US20210100746A1 - Method and devices for cellular transfer of compounds with augmented reality application - Google Patents
Method and devices for cellular transfer of compounds with augmented reality application Download PDFInfo
- Publication number
- US20210100746A1 US20210100746A1 US16/594,039 US201916594039A US2021100746A1 US 20210100746 A1 US20210100746 A1 US 20210100746A1 US 201916594039 A US201916594039 A US 201916594039A US 2021100746 A1 US2021100746 A1 US 2021100746A1
- Authority
- US
- United States
- Prior art keywords
- molecules
- aloe vera
- liposome
- constituents
- legal
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Abandoned
Links
- 150000001875 compounds Chemical class 0.000 title claims abstract description 70
- 238000000034 method Methods 0.000 title claims abstract description 29
- 238000012546 transfer Methods 0.000 title claims description 39
- 230000001413 cellular effect Effects 0.000 title claims description 32
- 230000003190 augmentative effect Effects 0.000 title claims description 17
- 239000002502 liposome Substances 0.000 claims abstract description 109
- 239000000470 constituent Substances 0.000 claims abstract description 36
- 229930003827 cannabinoid Natural products 0.000 claims abstract description 31
- 239000003557 cannabinoid Substances 0.000 claims abstract description 31
- 230000000699 topical effect Effects 0.000 claims abstract description 13
- 230000009286 beneficial effect Effects 0.000 claims abstract description 12
- 239000004615 ingredient Substances 0.000 claims abstract description 8
- 238000002156 mixing Methods 0.000 claims abstract description 8
- 230000037406 food intake Effects 0.000 claims abstract description 6
- 230000036541 health Effects 0.000 claims abstract description 3
- ZTGXAWYVTLUPDT-UHFFFAOYSA-N cannabidiol Natural products OC1=CC(CCCCC)=CC(O)=C1C1C(C(C)=C)CC=C(C)C1 ZTGXAWYVTLUPDT-UHFFFAOYSA-N 0.000 claims description 79
- QHMBSVQNZZTUGM-ZWKOTPCHSA-N cannabidiol Chemical compound OC1=CC(CCCCC)=CC(O)=C1[C@H]1[C@H](C(C)=C)CCC(C)=C1 QHMBSVQNZZTUGM-ZWKOTPCHSA-N 0.000 claims description 69
- QHMBSVQNZZTUGM-UHFFFAOYSA-N Trans-Cannabidiol Natural products OC1=CC(CCCCC)=CC(O)=C1C1C(C(C)=C)CCC(C)=C1 QHMBSVQNZZTUGM-UHFFFAOYSA-N 0.000 claims description 66
- 229950011318 cannabidiol Drugs 0.000 claims description 66
- PCXRACLQFPRCBB-ZWKOTPCHSA-N dihydrocannabidiol Natural products OC1=CC(CCCCC)=CC(O)=C1[C@H]1[C@H](C(C)C)CCC(C)=C1 PCXRACLQFPRCBB-ZWKOTPCHSA-N 0.000 claims description 66
- RHMXXJGYXNZAPX-UHFFFAOYSA-N emodin Chemical compound C1=C(O)C=C2C(=O)C3=CC(C)=CC(O)=C3C(=O)C2=C1O RHMXXJGYXNZAPX-UHFFFAOYSA-N 0.000 claims description 17
- XOYXESIZZFUVRD-UVSAJTFZSA-M acemannan Chemical compound CC(=O)O[C@@H]1[C@H](O)[C@@H](OC)O[C@H](CO)[C@H]1O[C@@H]1[C@@H](O)[C@@H](OC(C)=O)[C@H](O[C@@H]2[C@H]([C@@H](OC(C)=O)[C@H](O[C@@H]3[C@H]([C@@H](O)[C@H](O[C@@H]4[C@H]([C@@H](OC(C)=O)[C@H](O[C@@H]5[C@H]([C@@H](OC(C)=O)[C@H](O[C@@H]6[C@H]([C@@H](OC(C)=O)[C@H](O[C@@H]7[C@H]([C@@H](OC(C)=O)[C@H](OC)[C@@H](CO)O7)O)[C@@H](CO)O6)O)[C@H](O5)C([O-])=O)O)[C@@H](CO)O4)O)[C@@H](CO)O3)NC(C)=O)[C@@H](CO)O2)O)[C@@H](CO)O1 XOYXESIZZFUVRD-UVSAJTFZSA-M 0.000 claims description 15
- QXACEHWTBCFNSA-UHFFFAOYSA-N cannabigerol Natural products CCCCCC1=CC(O)=C(CC=C(C)CCC=C(C)C)C(O)=C1 QXACEHWTBCFNSA-UHFFFAOYSA-N 0.000 claims description 12
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 12
- VWDXGKUTGQJJHJ-UHFFFAOYSA-N Catenarin Natural products C1=C(O)C=C2C(=O)C3=C(O)C(C)=CC(O)=C3C(=O)C2=C1O VWDXGKUTGQJJHJ-UHFFFAOYSA-N 0.000 claims description 11
- 239000010282 Emodin Substances 0.000 claims description 11
- RBLJKYCRSCQLRP-UHFFFAOYSA-N Emodin-dianthron Natural products O=C1C2=CC(C)=CC(O)=C2C(=O)C2=C1CC(=O)C=C2O RBLJKYCRSCQLRP-UHFFFAOYSA-N 0.000 claims description 11
- YOOXNSPYGCZLAX-UHFFFAOYSA-N Helminthosporin Natural products C1=CC(O)=C2C(=O)C3=CC(C)=CC(O)=C3C(=O)C2=C1O YOOXNSPYGCZLAX-UHFFFAOYSA-N 0.000 claims description 11
- NTGIIKCGBNGQAR-UHFFFAOYSA-N Rheoemodin Natural products C1=C(O)C=C2C(=O)C3=CC(O)=CC(O)=C3C(=O)C2=C1O NTGIIKCGBNGQAR-UHFFFAOYSA-N 0.000 claims description 11
- 229960005327 acemannan Drugs 0.000 claims description 11
- VASFLQKDXBAWEL-UHFFFAOYSA-N emodin Natural products OC1=C(OC2=C(C=CC(=C2C1=O)O)O)C1=CC=C(C=C1)O VASFLQKDXBAWEL-UHFFFAOYSA-N 0.000 claims description 11
- PKUBGLYEOAJPEG-UHFFFAOYSA-N physcion Natural products C1=C(C)C=C2C(=O)C3=CC(C)=CC(O)=C3C(=O)C2=C1O PKUBGLYEOAJPEG-UHFFFAOYSA-N 0.000 claims description 11
- HKIKAXXIWJHWLY-ZIIYPAMZSA-N Aloesin Chemical compound C=12OC(CC(=O)C)=CC(=O)C2=C(C)C=C(O)C=1[C@@H]1O[C@H](CO)[C@@H](O)[C@H](O)[C@H]1O HKIKAXXIWJHWLY-ZIIYPAMZSA-N 0.000 claims description 9
- 241000282412 Homo Species 0.000 claims description 8
- QXACEHWTBCFNSA-SFQUDFHCSA-N cannabigerol Chemical compound CCCCCC1=CC(O)=C(C\C=C(/C)CCC=C(C)C)C(O)=C1 QXACEHWTBCFNSA-SFQUDFHCSA-N 0.000 claims description 8
- HKIKAXXIWJHWLY-QEVGBQTESA-N Aloesin Natural products O=C(CC=1Oc2c([C@H]3[C@H](O)[C@@H](O)[C@@H](O)[C@@H](CO)O3)c(O)cc(C)c2C(=O)C=1)C HKIKAXXIWJHWLY-QEVGBQTESA-N 0.000 claims description 6
- 230000007407 health benefit Effects 0.000 claims description 5
- 235000017807 phytochemicals Nutrition 0.000 claims description 3
- 229930000223 plant secondary metabolite Natural products 0.000 claims description 3
- 238000004088 simulation Methods 0.000 claims 1
- 239000007864 aqueous solution Substances 0.000 abstract description 8
- 238000003780 insertion Methods 0.000 abstract description 6
- 230000037431 insertion Effects 0.000 abstract description 6
- 239000007922 nasal spray Substances 0.000 abstract description 4
- 229940097496 nasal spray Drugs 0.000 abstract description 4
- 239000006218 nasal suppository Substances 0.000 abstract description 3
- CYQFCXCEBYINGO-IAGOWNOFSA-N delta1-THC Chemical compound C1=C(C)CC[C@H]2C(C)(C)OC3=CC(CCCCC)=CC(O)=C3[C@@H]21 CYQFCXCEBYINGO-IAGOWNOFSA-N 0.000 description 57
- 239000000047 product Substances 0.000 description 43
- 230000008901 benefit Effects 0.000 description 38
- CYQFCXCEBYINGO-UHFFFAOYSA-N THC Natural products C1=C(C)CCC2C(C)(C)OC3=CC(CCCCC)=CC(O)=C3C21 CYQFCXCEBYINGO-UHFFFAOYSA-N 0.000 description 36
- 229960004242 dronabinol Drugs 0.000 description 36
- 239000000126 substance Substances 0.000 description 33
- 241000218236 Cannabis Species 0.000 description 21
- 210000005260 human cell Anatomy 0.000 description 19
- 235000011399 aloe vera Nutrition 0.000 description 17
- 235000002961 Aloe barbadensis Nutrition 0.000 description 15
- 244000186892 Aloe vera Species 0.000 description 15
- 206010061218 Inflammation Diseases 0.000 description 15
- 230000004054 inflammatory process Effects 0.000 description 15
- 150000002632 lipids Chemical class 0.000 description 15
- 238000005538 encapsulation Methods 0.000 description 13
- 238000010586 diagram Methods 0.000 description 12
- 208000024891 symptom Diseases 0.000 description 11
- 238000011282 treatment Methods 0.000 description 11
- UVOLYTDXHDXWJU-NRFANRHFSA-N Cannabichromene Natural products C1=C[C@](C)(CCC=C(C)C)OC2=CC(CCCCC)=CC(O)=C21 UVOLYTDXHDXWJU-NRFANRHFSA-N 0.000 description 10
- 208000002193 Pain Diseases 0.000 description 10
- 210000003491 skin Anatomy 0.000 description 10
- 230000037303 wrinkles Effects 0.000 description 10
- 101100268917 Oryctolagus cuniculus ACOX2 gene Proteins 0.000 description 9
- UCONUSSAWGCZMV-UHFFFAOYSA-N Tetrahydro-cannabinol-carbonsaeure Natural products O1C(C)(C)C2CCC(C)=CC2C2=C1C=C(CCCCC)C(C(O)=O)=C2O UCONUSSAWGCZMV-UHFFFAOYSA-N 0.000 description 9
- 230000008569 process Effects 0.000 description 9
- ZROLHBHDLIHEMS-HUUCEWRRSA-N (6ar,10ar)-6,6,9-trimethyl-3-propyl-6a,7,8,10a-tetrahydrobenzo[c]chromen-1-ol Chemical compound C1=C(C)CC[C@H]2C(C)(C)OC3=CC(CCC)=CC(O)=C3[C@@H]21 ZROLHBHDLIHEMS-HUUCEWRRSA-N 0.000 description 8
- 206010028980 Neoplasm Diseases 0.000 description 8
- 230000003110 anti-inflammatory effect Effects 0.000 description 8
- 201000011510 cancer Diseases 0.000 description 8
- 208000006096 Attention Deficit Disorder with Hyperactivity Diseases 0.000 description 7
- -1 CBD compound Chemical class 0.000 description 7
- 210000004027 cell Anatomy 0.000 description 7
- 230000002209 hydrophobic effect Effects 0.000 description 7
- 239000000463 material Substances 0.000 description 7
- 239000012528 membrane Substances 0.000 description 7
- 229940100611 topical cream Drugs 0.000 description 7
- 208000036864 Attention deficit/hyperactivity disease Diseases 0.000 description 6
- 150000004056 anthraquinones Chemical class 0.000 description 6
- 208000015802 attention deficit-hyperactivity disease Diseases 0.000 description 6
- 230000000694 effects Effects 0.000 description 6
- 210000001061 forehead Anatomy 0.000 description 6
- 238000012545 processing Methods 0.000 description 6
- UVOLYTDXHDXWJU-UHFFFAOYSA-N Cannabichromene Chemical compound C1=CC(C)(CCC=C(C)C)OC2=CC(CCCCC)=CC(O)=C21 UVOLYTDXHDXWJU-UHFFFAOYSA-N 0.000 description 5
- 241000196324 Embryophyta Species 0.000 description 5
- 230000000844 anti-bacterial effect Effects 0.000 description 5
- WVOLTBSCXRRQFR-DLBZAZTESA-M cannabidiolate Chemical compound OC1=C(C([O-])=O)C(CCCCC)=CC(O)=C1[C@H]1[C@H](C(C)=C)CCC(C)=C1 WVOLTBSCXRRQFR-DLBZAZTESA-M 0.000 description 5
- 230000010261 cell growth Effects 0.000 description 5
- 235000000346 sugar Nutrition 0.000 description 5
- 239000011782 vitamin Substances 0.000 description 5
- 235000013343 vitamin Nutrition 0.000 description 5
- 229930003231 vitamin Natural products 0.000 description 5
- 229940088594 vitamin Drugs 0.000 description 5
- WVOLTBSCXRRQFR-SJORKVTESA-N Cannabidiolic acid Natural products OC1=C(C(O)=O)C(CCCCC)=CC(O)=C1[C@@H]1[C@@H](C(C)=C)CCC(C)=C1 WVOLTBSCXRRQFR-SJORKVTESA-N 0.000 description 4
- ZROLHBHDLIHEMS-UHFFFAOYSA-N Delta9 tetrahydrocannabivarin Natural products C1=C(C)CCC2C(C)(C)OC3=CC(CCC)=CC(O)=C3C21 ZROLHBHDLIHEMS-UHFFFAOYSA-N 0.000 description 4
- 102000004190 Enzymes Human genes 0.000 description 4
- 108090000790 Enzymes Proteins 0.000 description 4
- 208000021384 Obsessive-Compulsive disease Diseases 0.000 description 4
- 206010002026 amyotrophic lateral sclerosis Diseases 0.000 description 4
- 230000003078 antioxidant effect Effects 0.000 description 4
- 206010003246 arthritis Diseases 0.000 description 4
- 239000006071 cream Substances 0.000 description 4
- 229940088598 enzyme Drugs 0.000 description 4
- 210000003128 head Anatomy 0.000 description 4
- 208000035231 inattentive type attention deficit hyperactivity disease Diseases 0.000 description 4
- 229910052500 inorganic mineral Inorganic materials 0.000 description 4
- 238000004519 manufacturing process Methods 0.000 description 4
- 239000011707 mineral Substances 0.000 description 4
- 239000000203 mixture Substances 0.000 description 4
- 208000028173 post-traumatic stress disease Diseases 0.000 description 4
- YGSDEFSMJLZEOE-UHFFFAOYSA-N salicylic acid Chemical compound OC(=O)C1=CC=CC=C1O YGSDEFSMJLZEOE-UHFFFAOYSA-N 0.000 description 4
- 208000019901 Anxiety disease Diseases 0.000 description 3
- 206010010904 Convulsion Diseases 0.000 description 3
- 229920002581 Glucomannan Polymers 0.000 description 3
- 206010020772 Hypertension Diseases 0.000 description 3
- 206010028813 Nausea Diseases 0.000 description 3
- 238000010521 absorption reaction Methods 0.000 description 3
- 150000001413 amino acids Chemical class 0.000 description 3
- 239000003963 antioxidant agent Substances 0.000 description 3
- 235000006708 antioxidants Nutrition 0.000 description 3
- 230000036506 anxiety Effects 0.000 description 3
- 238000013473 artificial intelligence Methods 0.000 description 3
- 235000013361 beverage Nutrition 0.000 description 3
- 210000004369 blood Anatomy 0.000 description 3
- 239000008280 blood Substances 0.000 description 3
- 230000008468 bone growth Effects 0.000 description 3
- 206010012601 diabetes mellitus Diseases 0.000 description 3
- 201000006549 dyspepsia Diseases 0.000 description 3
- 238000009472 formulation Methods 0.000 description 3
- 230000006870 function Effects 0.000 description 3
- 239000000499 gel Substances 0.000 description 3
- 150000004676 glycans Chemical class 0.000 description 3
- 230000008693 nausea Effects 0.000 description 3
- 230000000149 penetrating effect Effects 0.000 description 3
- 229920001282 polysaccharide Polymers 0.000 description 3
- 239000005017 polysaccharide Substances 0.000 description 3
- 150000008163 sugars Chemical class 0.000 description 3
- 239000011800 void material Substances 0.000 description 3
- 230000029663 wound healing Effects 0.000 description 3
- 241001116389 Aloe Species 0.000 description 2
- YDQWDHRMZQUTBA-UHFFFAOYSA-N Aloe emodin Chemical compound C1=CC=C2C(=O)C3=CC(CO)=CC(O)=C3C(=O)C2=C1O YDQWDHRMZQUTBA-UHFFFAOYSA-N 0.000 description 2
- 206010006895 Cachexia Diseases 0.000 description 2
- 244000025254 Cannabis sativa Species 0.000 description 2
- 208000011231 Crohn disease Diseases 0.000 description 2
- 208000018522 Gastrointestinal disease Diseases 0.000 description 2
- 208000010412 Glaucoma Diseases 0.000 description 2
- WQZGKKKJIJFFOK-GASJEMHNSA-N Glucose Natural products OC[C@H]1OC(O)[C@H](O)[C@@H](O)[C@@H]1O WQZGKKKJIJFFOK-GASJEMHNSA-N 0.000 description 2
- 206010022489 Insulin Resistance Diseases 0.000 description 2
- 102000043136 MAP kinase family Human genes 0.000 description 2
- 108091054455 MAP kinase family Proteins 0.000 description 2
- 208000007101 Muscle Cramp Diseases 0.000 description 2
- FPIPGXGPPPQFEQ-OVSJKPMPSA-N all-trans-retinol Chemical compound OC\C=C(/C)\C=C\C=C(/C)\C=C\C1=C(C)CCCC1(C)C FPIPGXGPPPQFEQ-OVSJKPMPSA-N 0.000 description 2
- 230000000202 analgesic effect Effects 0.000 description 2
- 208000022531 anorexia Diseases 0.000 description 2
- 230000003712 anti-aging effect Effects 0.000 description 2
- 230000002421 anti-septic effect Effects 0.000 description 2
- 230000004596 appetite loss Effects 0.000 description 2
- 208000006673 asthma Diseases 0.000 description 2
- 230000001580 bacterial effect Effects 0.000 description 2
- 230000006399 behavior Effects 0.000 description 2
- 230000015572 biosynthetic process Effects 0.000 description 2
- HRHJHXJQMNWQTF-UHFFFAOYSA-N cannabichromenic acid Chemical compound O1C(C)(CCC=C(C)C)C=CC2=C1C=C(CCCCC)C(C(O)=O)=C2O HRHJHXJQMNWQTF-UHFFFAOYSA-N 0.000 description 2
- 229910052799 carbon Inorganic materials 0.000 description 2
- 125000004432 carbon atom Chemical group C* 0.000 description 2
- 230000008859 change Effects 0.000 description 2
- HVYWMOMLDIMFJA-DPAQBDIFSA-N cholesterol Chemical compound C1C=C2C[C@@H](O)CC[C@]2(C)[C@@H]2[C@@H]1[C@@H]1CC[C@H]([C@H](C)CCCC(C)C)[C@@]1(C)CC2 HVYWMOMLDIMFJA-DPAQBDIFSA-N 0.000 description 2
- 239000002537 cosmetic Substances 0.000 description 2
- 125000004122 cyclic group Chemical group 0.000 description 2
- 206010061428 decreased appetite Diseases 0.000 description 2
- 235000014113 dietary fatty acids Nutrition 0.000 description 2
- 239000003925 fat Substances 0.000 description 2
- 206010016256 fatigue Diseases 0.000 description 2
- 229930195729 fatty acid Natural products 0.000 description 2
- 239000000194 fatty acid Substances 0.000 description 2
- 150000004665 fatty acids Chemical class 0.000 description 2
- OVBPIULPVIDEAO-LBPRGKRZSA-N folic acid Chemical compound C=1N=C2NC(N)=NC(=O)C2=NC=1CNC1=CC=C(C(=O)N[C@@H](CCC(O)=O)C(O)=O)C=C1 OVBPIULPVIDEAO-LBPRGKRZSA-N 0.000 description 2
- 239000008103 glucose Substances 0.000 description 2
- 230000012010 growth Effects 0.000 description 2
- 230000035876 healing Effects 0.000 description 2
- 208000024798 heartburn Diseases 0.000 description 2
- 208000014617 hemorrhoid Diseases 0.000 description 2
- 229920005610 lignin Polymers 0.000 description 2
- 239000007788 liquid Substances 0.000 description 2
- PKGKOZOYXQMJNG-UHFFFAOYSA-N lupeol Natural products CC(=C)C1CC2C(C)(CCC3C4(C)CCC5C(C)(C)C(O)CCC5(C)C4CCC23C)C1 PKGKOZOYXQMJNG-UHFFFAOYSA-N 0.000 description 2
- MQYXUWHLBZFQQO-QGTGJCAVSA-N lupeol Chemical compound C1C[C@H](O)C(C)(C)[C@@H]2CC[C@@]3(C)[C@]4(C)CC[C@@]5(C)CC[C@@H](C(=C)C)[C@@H]5[C@H]4CC[C@@H]3[C@]21C MQYXUWHLBZFQQO-QGTGJCAVSA-N 0.000 description 2
- 150000002772 monosaccharides Chemical class 0.000 description 2
- 230000036651 mood Effects 0.000 description 2
- 201000006938 muscular dystrophy Diseases 0.000 description 2
- 235000015097 nutrients Nutrition 0.000 description 2
- 239000002674 ointment Substances 0.000 description 2
- FJKROLUGYXJWQN-UHFFFAOYSA-N papa-hydroxy-benzoic acid Natural products OC(=O)C1=CC=C(O)C=C1 FJKROLUGYXJWQN-UHFFFAOYSA-N 0.000 description 2
- 150000002989 phenols Chemical class 0.000 description 2
- 229960004889 salicylic acid Drugs 0.000 description 2
- 229930182490 saponin Natural products 0.000 description 2
- 150000007949 saponins Chemical class 0.000 description 2
- 235000017709 saponins Nutrition 0.000 description 2
- 230000019491 signal transduction Effects 0.000 description 2
- 239000007921 spray Substances 0.000 description 2
- 230000001954 sterilising effect Effects 0.000 description 2
- 230000035882 stress Effects 0.000 description 2
- 230000008685 targeting Effects 0.000 description 2
- 208000001072 type 2 diabetes mellitus Diseases 0.000 description 2
- LUEWUZLMQUOBSB-FSKGGBMCSA-N (2s,3s,4s,5s,6r)-2-[(2r,3s,4r,5r,6s)-6-[(2r,3s,4r,5s,6s)-4,5-dihydroxy-2-(hydroxymethyl)-6-[(2r,4r,5s,6r)-4,5,6-trihydroxy-2-(hydroxymethyl)oxan-3-yl]oxyoxan-3-yl]oxy-4,5-dihydroxy-2-(hydroxymethyl)oxan-3-yl]oxy-6-(hydroxymethyl)oxane-3,4,5-triol Chemical compound O[C@H]1[C@@H](O)[C@H](O)[C@@H](CO)O[C@H]1O[C@@H]1[C@@H](CO)O[C@@H](O[C@@H]2[C@H](O[C@@H](OC3[C@H](O[C@@H](O)[C@@H](O)[C@H]3O)CO)[C@@H](O)[C@H]2O)CO)[C@H](O)[C@H]1O LUEWUZLMQUOBSB-FSKGGBMCSA-N 0.000 description 1
- FPIPGXGPPPQFEQ-UHFFFAOYSA-N 13-cis retinol Natural products OCC=C(C)C=CC=C(C)C=CC1=C(C)CCCC1(C)C FPIPGXGPPPQFEQ-UHFFFAOYSA-N 0.000 description 1
- 208000002874 Acne Vulgaris Diseases 0.000 description 1
- 102000011690 Adiponectin Human genes 0.000 description 1
- 108010076365 Adiponectin Proteins 0.000 description 1
- 102000002260 Alkaline Phosphatase Human genes 0.000 description 1
- 108020004774 Alkaline Phosphatase Proteins 0.000 description 1
- AFHJQYHRLPMKHU-XXWVOBANSA-N Aloin Natural products O=C1c2c(O)cc(CO)cc2[C@H]([C@H]2[C@H](O)[C@@H](O)[C@@H](O)[C@@H](CO)O2)c2c1c(O)ccc2 AFHJQYHRLPMKHU-XXWVOBANSA-N 0.000 description 1
- 201000004384 Alopecia Diseases 0.000 description 1
- 239000004382 Amylase Substances 0.000 description 1
- 102000013142 Amylases Human genes 0.000 description 1
- 108010065511 Amylases Proteins 0.000 description 1
- 208000023275 Autoimmune disease Diseases 0.000 description 1
- 229930192334 Auxin Natural products 0.000 description 1
- 206010006187 Breast cancer Diseases 0.000 description 1
- 208000026310 Breast neoplasm Diseases 0.000 description 1
- 210000001239 CD8-positive, alpha-beta cytotoxic T lymphocyte Anatomy 0.000 description 1
- OYPRJOBELJOOCE-UHFFFAOYSA-N Calcium Chemical compound [Ca] OYPRJOBELJOOCE-UHFFFAOYSA-N 0.000 description 1
- SGNBVLSWZMBQTH-FGAXOLDCSA-N Campesterol Natural products O[C@@H]1CC=2[C@@](C)([C@@H]3[C@H]([C@H]4[C@@](C)([C@H]([C@H](CC[C@H](C(C)C)C)C)CC4)CC3)CC=2)CC1 SGNBVLSWZMBQTH-FGAXOLDCSA-N 0.000 description 1
- 235000012766 Cannabis sativa ssp. sativa var. sativa Nutrition 0.000 description 1
- 235000012765 Cannabis sativa ssp. sativa var. spontanea Nutrition 0.000 description 1
- 102000005367 Carboxypeptidases Human genes 0.000 description 1
- 108010006303 Carboxypeptidases Proteins 0.000 description 1
- 102000016938 Catalase Human genes 0.000 description 1
- 108010053835 Catalase Proteins 0.000 description 1
- 108010059892 Cellulase Proteins 0.000 description 1
- VYZAMTAEIAYCRO-UHFFFAOYSA-N Chromium Chemical compound [Cr] VYZAMTAEIAYCRO-UHFFFAOYSA-N 0.000 description 1
- 208000035473 Communicable disease Diseases 0.000 description 1
- RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 description 1
- NBSCHQHZLSJFNQ-QTVWNMPRSA-N D-Mannose-6-phosphate Chemical group OC1O[C@H](COP(O)(O)=O)[C@@H](O)[C@H](O)[C@@H]1O NBSCHQHZLSJFNQ-QTVWNMPRSA-N 0.000 description 1
- 208000002064 Dental Plaque Diseases 0.000 description 1
- 208000020401 Depressive disease Diseases 0.000 description 1
- 201000004624 Dermatitis Diseases 0.000 description 1
- 206010012438 Dermatitis atopic Diseases 0.000 description 1
- 208000001640 Fibromyalgia Diseases 0.000 description 1
- 229930091371 Fructose Natural products 0.000 description 1
- 239000005715 Fructose Substances 0.000 description 1
- RFSUNEUAIZKAJO-ARQDHWQXSA-N Fructose Chemical compound OC[C@H]1O[C@](O)(CO)[C@@H](O)[C@@H]1O RFSUNEUAIZKAJO-ARQDHWQXSA-N 0.000 description 1
- 206010017533 Fungal infection Diseases 0.000 description 1
- 229930191978 Gibberellin Natural products 0.000 description 1
- 102000003886 Glycoproteins Human genes 0.000 description 1
- 108090000288 Glycoproteins Proteins 0.000 description 1
- 229920002683 Glycosaminoglycan Polymers 0.000 description 1
- BTEISVKTSQLKST-UHFFFAOYSA-N Haliclonasterol Natural products CC(C=CC(C)C(C)(C)C)C1CCC2C3=CC=C4CC(O)CCC4(C)C3CCC12C BTEISVKTSQLKST-UHFFFAOYSA-N 0.000 description 1
- 206010019233 Headaches Diseases 0.000 description 1
- 206010019280 Heart failures Diseases 0.000 description 1
- 206010020601 Hyperchlorhydria Diseases 0.000 description 1
- 206010020751 Hypersensitivity Diseases 0.000 description 1
- DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 description 1
- 208000022559 Inflammatory bowel disease Diseases 0.000 description 1
- 102000014150 Interferons Human genes 0.000 description 1
- 108010050904 Interferons Proteins 0.000 description 1
- 102000015696 Interleukins Human genes 0.000 description 1
- 108010063738 Interleukins Proteins 0.000 description 1
- 239000004166 Lanolin Substances 0.000 description 1
- 102000004856 Lectins Human genes 0.000 description 1
- 108090001090 Lectins Proteins 0.000 description 1
- 102000004882 Lipase Human genes 0.000 description 1
- 108090001060 Lipase Proteins 0.000 description 1
- 239000004367 Lipase Substances 0.000 description 1
- 239000000232 Lipid Bilayer Substances 0.000 description 1
- FYYHWMGAXLPEAU-UHFFFAOYSA-N Magnesium Chemical compound [Mg] FYYHWMGAXLPEAU-UHFFFAOYSA-N 0.000 description 1
- 229920000057 Mannan Polymers 0.000 description 1
- 206010027476 Metastases Diseases 0.000 description 1
- 208000019695 Migraine disease Diseases 0.000 description 1
- 229920000715 Mucilage Polymers 0.000 description 1
- 208000008238 Muscle Spasticity Diseases 0.000 description 1
- 208000031888 Mycoses Diseases 0.000 description 1
- OVBPIULPVIDEAO-UHFFFAOYSA-N N-Pteroyl-L-glutaminsaeure Natural products C=1N=C2NC(N)=NC(=O)C2=NC=1CNC1=CC=C(C(=O)NC(CCC(O)=O)C(O)=O)C=C1 OVBPIULPVIDEAO-UHFFFAOYSA-N 0.000 description 1
- 208000012902 Nervous system disease Diseases 0.000 description 1
- 208000025966 Neurological disease Diseases 0.000 description 1
- 208000001132 Osteoporosis Diseases 0.000 description 1
- 206010033128 Ovarian cancer Diseases 0.000 description 1
- 206010061535 Ovarian neoplasm Diseases 0.000 description 1
- 208000008469 Peptic Ulcer Diseases 0.000 description 1
- 102000003992 Peroxidases Human genes 0.000 description 1
- 208000004983 Phantom Limb Diseases 0.000 description 1
- 241000223960 Plasmodium falciparum Species 0.000 description 1
- ZLMJMSJWJFRBEC-UHFFFAOYSA-N Potassium Chemical compound [K] ZLMJMSJWJFRBEC-UHFFFAOYSA-N 0.000 description 1
- 201000004681 Psoriasis Diseases 0.000 description 1
- 201000001263 Psoriatic Arthritis Diseases 0.000 description 1
- 208000036824 Psoriatic arthropathy Diseases 0.000 description 1
- 206010037660 Pyrexia Diseases 0.000 description 1
- BUGBHKTXTAQXES-UHFFFAOYSA-N Selenium Chemical compound [Se] BUGBHKTXTAQXES-UHFFFAOYSA-N 0.000 description 1
- 206010072170 Skin wound Diseases 0.000 description 1
- 208000013738 Sleep Initiation and Maintenance disease Diseases 0.000 description 1
- 208000005392 Spasm Diseases 0.000 description 1
- 208000020339 Spinal injury Diseases 0.000 description 1
- 206010042496 Sunburn Diseases 0.000 description 1
- 210000001744 T-lymphocyte Anatomy 0.000 description 1
- 206010067584 Type 1 diabetes mellitus Diseases 0.000 description 1
- 230000006750 UV protection Effects 0.000 description 1
- 241000700605 Viruses Species 0.000 description 1
- 229930003779 Vitamin B12 Natural products 0.000 description 1
- 206010047700 Vomiting Diseases 0.000 description 1
- 208000027418 Wounds and injury Diseases 0.000 description 1
- HCHKCACWOHOZIP-UHFFFAOYSA-N Zinc Chemical compound [Zn] HCHKCACWOHOZIP-UHFFFAOYSA-N 0.000 description 1
- 206010000496 acne Diseases 0.000 description 1
- 239000004480 active ingredient Substances 0.000 description 1
- 239000000853 adhesive Substances 0.000 description 1
- 230000032683 aging Effects 0.000 description 1
- 229930013930 alkaloid Natural products 0.000 description 1
- OENHQHLEOONYIE-UKMVMLAPSA-N all-trans beta-carotene Natural products CC=1CCCC(C)(C)C=1/C=C/C(/C)=C/C=C/C(/C)=C/C=C/C=C(C)C=CC=C(C)C=CC1=C(C)CCCC1(C)C OENHQHLEOONYIE-UKMVMLAPSA-N 0.000 description 1
- CPUHNROBVJNNPW-UHFFFAOYSA-N aloin A Natural products OC1C(O)C(O)C(CO)OC1OC1C2=CC(CO)=CC(O)=C2C(=O)C2=C(O)C=CC=C21 CPUHNROBVJNNPW-UHFFFAOYSA-N 0.000 description 1
- AFHJQYHRLPMKHU-WEZNYRQKSA-N aloin B Chemical compound O[C@@H]1[C@@H](O)[C@H](O)[C@@H](CO)O[C@H]1[C@H]1C2=CC(CO)=CC(O)=C2C(=O)C2=C(O)C=CC=C21 AFHJQYHRLPMKHU-WEZNYRQKSA-N 0.000 description 1
- 239000009581 alprogen Substances 0.000 description 1
- 235000019418 amylase Nutrition 0.000 description 1
- 229940035676 analgesics Drugs 0.000 description 1
- 239000000730 antalgic agent Substances 0.000 description 1
- 230000003266 anti-allergic effect Effects 0.000 description 1
- 230000001093 anti-cancer Effects 0.000 description 1
- 230000002082 anti-convulsion Effects 0.000 description 1
- 230000003178 anti-diabetic effect Effects 0.000 description 1
- 230000000078 anti-malarial effect Effects 0.000 description 1
- 230000001203 anti-plasmodial effect Effects 0.000 description 1
- 230000001153 anti-wrinkle effect Effects 0.000 description 1
- 229940088710 antibiotic agent Drugs 0.000 description 1
- 239000003472 antidiabetic agent Substances 0.000 description 1
- 239000003430 antimalarial agent Substances 0.000 description 1
- 239000003443 antiviral agent Substances 0.000 description 1
- 229940121357 antivirals Drugs 0.000 description 1
- 239000002948 appetite stimulant Substances 0.000 description 1
- 210000001367 artery Anatomy 0.000 description 1
- 230000002917 arthritic effect Effects 0.000 description 1
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 1
- 201000008937 atopic dermatitis Diseases 0.000 description 1
- 208000010668 atopic eczema Diseases 0.000 description 1
- 239000002363 auxin Substances 0.000 description 1
- 244000052616 bacterial pathogen Species 0.000 description 1
- WQZGKKKJIJFFOK-VFUOTHLCSA-N beta-D-glucose Chemical compound OC[C@H]1O[C@@H](O)[C@H](O)[C@@H](O)[C@@H]1O WQZGKKKJIJFFOK-VFUOTHLCSA-N 0.000 description 1
- 235000013734 beta-carotene Nutrition 0.000 description 1
- 239000011648 beta-carotene Substances 0.000 description 1
- TUPZEYHYWIEDIH-WAIFQNFQSA-N beta-carotene Natural products CC(=C/C=C/C=C(C)/C=C/C=C(C)/C=C/C1=C(C)CCCC1(C)C)C=CC=C(/C)C=CC2=CCCCC2(C)C TUPZEYHYWIEDIH-WAIFQNFQSA-N 0.000 description 1
- 229960002747 betacarotene Drugs 0.000 description 1
- 230000004071 biological effect Effects 0.000 description 1
- 230000036772 blood pressure Effects 0.000 description 1
- 210000001185 bone marrow Anatomy 0.000 description 1
- 239000006227 byproduct Substances 0.000 description 1
- 239000011575 calcium Substances 0.000 description 1
- 229910052791 calcium Inorganic materials 0.000 description 1
- 235000009120 camo Nutrition 0.000 description 1
- SGNBVLSWZMBQTH-PODYLUTMSA-N campesterol Chemical compound C1C=C2C[C@@H](O)CC[C@]2(C)[C@@H]2[C@@H]1[C@@H]1CC[C@H]([C@H](C)CC[C@@H](C)C(C)C)[C@@]1(C)CC2 SGNBVLSWZMBQTH-PODYLUTMSA-N 0.000 description 1
- 235000000431 campesterol Nutrition 0.000 description 1
- SEEZIOZEUUMJME-FOWTUZBSSA-N cannabigerolic acid Chemical group CCCCCC1=CC(O)=C(C\C=C(/C)CCC=C(C)C)C(O)=C1C(O)=O SEEZIOZEUUMJME-FOWTUZBSSA-N 0.000 description 1
- SEEZIOZEUUMJME-UHFFFAOYSA-N cannabinerolic acid Natural products CCCCCC1=CC(O)=C(CC=C(C)CCC=C(C)C)C(O)=C1C(O)=O SEEZIOZEUUMJME-UHFFFAOYSA-N 0.000 description 1
- 229940065144 cannabinoids Drugs 0.000 description 1
- 239000002775 capsule Substances 0.000 description 1
- 229940077731 carbohydrate nutrients Drugs 0.000 description 1
- 150000001720 carbohydrates Chemical class 0.000 description 1
- 235000014633 carbohydrates Nutrition 0.000 description 1
- 230000015556 catabolic process Effects 0.000 description 1
- 230000019522 cellular metabolic process Effects 0.000 description 1
- 229940106157 cellulase Drugs 0.000 description 1
- 235000005607 chanvre indien Nutrition 0.000 description 1
- 235000012000 cholesterol Nutrition 0.000 description 1
- OEYIOHPDSNJKLS-UHFFFAOYSA-N choline Chemical compound C[N+](C)(C)CCO OEYIOHPDSNJKLS-UHFFFAOYSA-N 0.000 description 1
- 229960001231 choline Drugs 0.000 description 1
- 239000011651 chromium Substances 0.000 description 1
- 229910052804 chromium Inorganic materials 0.000 description 1
- FDJOLVPMNUYSCM-WZHZPDAFSA-L cobalt(3+);[(2r,3s,4r,5s)-5-(5,6-dimethylbenzimidazol-1-yl)-4-hydroxy-2-(hydroxymethyl)oxolan-3-yl] [(2r)-1-[3-[(1r,2r,3r,4z,7s,9z,12s,13s,14z,17s,18s,19r)-2,13,18-tris(2-amino-2-oxoethyl)-7,12,17-tris(3-amino-3-oxopropyl)-3,5,8,8,13,15,18,19-octamethyl-2 Chemical compound [Co+3].N#[C-].N([C@@H]([C@]1(C)[N-]\C([C@H]([C@@]1(CC(N)=O)C)CCC(N)=O)=C(\C)/C1=N/C([C@H]([C@@]1(CC(N)=O)C)CCC(N)=O)=C\C1=N\C([C@H](C1(C)C)CCC(N)=O)=C/1C)[C@@H]2CC(N)=O)=C\1[C@]2(C)CCC(=O)NC[C@@H](C)OP([O-])(=O)O[C@H]1[C@@H](O)[C@@H](N2C3=CC(C)=C(C)C=C3N=C2)O[C@@H]1CO FDJOLVPMNUYSCM-WZHZPDAFSA-L 0.000 description 1
- 206010009887 colitis Diseases 0.000 description 1
- 230000008602 contraction Effects 0.000 description 1
- 230000036461 convulsion Effects 0.000 description 1
- 229910052802 copper Inorganic materials 0.000 description 1
- 239000010949 copper Substances 0.000 description 1
- 230000006378 damage Effects 0.000 description 1
- 238000002716 delivery method Methods 0.000 description 1
- 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 description 1
- 208000035475 disorder Diseases 0.000 description 1
- 208000000718 duodenal ulcer Diseases 0.000 description 1
- 206010015037 epilepsy Diseases 0.000 description 1
- 239000003797 essential amino acid Substances 0.000 description 1
- 235000020776 essential amino acid Nutrition 0.000 description 1
- 238000011156 evaluation Methods 0.000 description 1
- 238000005562 fading Methods 0.000 description 1
- 239000012467 final product Substances 0.000 description 1
- 235000021554 flavoured beverage Nutrition 0.000 description 1
- 235000019152 folic acid Nutrition 0.000 description 1
- 229960000304 folic acid Drugs 0.000 description 1
- 239000011724 folic acid Substances 0.000 description 1
- 210000002683 foot Anatomy 0.000 description 1
- 235000011389 fruit/vegetable juice Nutrition 0.000 description 1
- 230000002496 gastric effect Effects 0.000 description 1
- 210000001035 gastrointestinal tract Anatomy 0.000 description 1
- 239000003448 gibberellin Substances 0.000 description 1
- IXORZMNAPKEEDV-OBDJNFEBSA-N gibberellin A3 Chemical class C([C@@]1(O)C(=C)C[C@@]2(C1)[C@H]1C(O)=O)C[C@H]2[C@]2(C=C[C@@H]3O)[C@H]1[C@]3(C)C(=O)O2 IXORZMNAPKEEDV-OBDJNFEBSA-N 0.000 description 1
- 229940046240 glucomannan Drugs 0.000 description 1
- 208000024963 hair loss Diseases 0.000 description 1
- 230000003676 hair loss Effects 0.000 description 1
- 210000004247 hand Anatomy 0.000 description 1
- 231100000869 headache Toxicity 0.000 description 1
- 239000011487 hemp Substances 0.000 description 1
- 230000002440 hepatic effect Effects 0.000 description 1
- 235000012907 honey Nutrition 0.000 description 1
- 239000005556 hormone Substances 0.000 description 1
- 229940088597 hormone Drugs 0.000 description 1
- 125000002887 hydroxy group Chemical group [H]O* 0.000 description 1
- 210000000987 immune system Anatomy 0.000 description 1
- 230000036039 immunity Effects 0.000 description 1
- 230000004968 inflammatory condition Effects 0.000 description 1
- 230000005764 inhibitory process Effects 0.000 description 1
- 208000014674 injury Diseases 0.000 description 1
- 150000002484 inorganic compounds Chemical class 0.000 description 1
- 229910010272 inorganic material Inorganic materials 0.000 description 1
- 206010022437 insomnia Diseases 0.000 description 1
- 229940079322 interferon Drugs 0.000 description 1
- 229940047122 interleukins Drugs 0.000 description 1
- 208000028774 intestinal disease Diseases 0.000 description 1
- AFHJQYHRLPMKHU-UHFFFAOYSA-N isobarbaloin Natural products OC1C(O)C(O)C(CO)OC1C1C2=CC(CO)=CC(O)=C2C(=O)C2=C(O)C=CC=C21 AFHJQYHRLPMKHU-UHFFFAOYSA-N 0.000 description 1
- 230000005722 itchiness Effects 0.000 description 1
- 230000003907 kidney function Effects 0.000 description 1
- 210000003127 knee Anatomy 0.000 description 1
- 229940039717 lanolin Drugs 0.000 description 1
- 235000019388 lanolin Nutrition 0.000 description 1
- 239000008141 laxative Substances 0.000 description 1
- 229940125722 laxative agent Drugs 0.000 description 1
- 239000002523 lectin Substances 0.000 description 1
- 210000002414 leg Anatomy 0.000 description 1
- 230000003902 lesion Effects 0.000 description 1
- 235000019421 lipase Nutrition 0.000 description 1
- 238000005461 lubrication Methods 0.000 description 1
- 239000011777 magnesium Substances 0.000 description 1
- 229910052749 magnesium Inorganic materials 0.000 description 1
- 201000004792 malaria Diseases 0.000 description 1
- WPBNNNQJVZRUHP-UHFFFAOYSA-L manganese(2+);methyl n-[[2-(methoxycarbonylcarbamothioylamino)phenyl]carbamothioyl]carbamate;n-[2-(sulfidocarbothioylamino)ethyl]carbamodithioate Chemical compound [Mn+2].[S-]C(=S)NCCNC([S-])=S.COC(=O)NC(=S)NC1=CC=CC=C1NC(=S)NC(=O)OC WPBNNNQJVZRUHP-UHFFFAOYSA-L 0.000 description 1
- 230000009401 metastasis Effects 0.000 description 1
- 206010027599 migraine Diseases 0.000 description 1
- 238000012544 monitoring process Methods 0.000 description 1
- 210000001616 monocyte Anatomy 0.000 description 1
- 201000006417 multiple sclerosis Diseases 0.000 description 1
- 210000003205 muscle Anatomy 0.000 description 1
- 230000000926 neurological effect Effects 0.000 description 1
- 230000000324 neuroprotective effect Effects 0.000 description 1
- 239000003921 oil Substances 0.000 description 1
- 150000007524 organic acids Chemical class 0.000 description 1
- 235000005985 organic acids Nutrition 0.000 description 1
- 229910052760 oxygen Inorganic materials 0.000 description 1
- 239000001301 oxygen Substances 0.000 description 1
- 238000004806 packaging method and process Methods 0.000 description 1
- 229940124641 pain reliever Drugs 0.000 description 1
- 244000045947 parasite Species 0.000 description 1
- 230000001175 peptic effect Effects 0.000 description 1
- 108040007629 peroxidase activity proteins Proteins 0.000 description 1
- 150000003904 phospholipids Chemical class 0.000 description 1
- 239000006187 pill Substances 0.000 description 1
- 239000011591 potassium Substances 0.000 description 1
- 229910052700 potassium Inorganic materials 0.000 description 1
- 239000000843 powder Substances 0.000 description 1
- 238000002360 preparation method Methods 0.000 description 1
- 239000006215 rectal suppository Substances 0.000 description 1
- 230000004044 response Effects 0.000 description 1
- 235000020944 retinol Nutrition 0.000 description 1
- 239000011607 retinol Substances 0.000 description 1
- 229960003471 retinol Drugs 0.000 description 1
- 206010039073 rheumatoid arthritis Diseases 0.000 description 1
- 150000003870 salicylic acids Chemical class 0.000 description 1
- 230000037390 scarring Effects 0.000 description 1
- 229930000044 secondary metabolite Natural products 0.000 description 1
- 239000011669 selenium Substances 0.000 description 1
- 229910052711 selenium Inorganic materials 0.000 description 1
- 230000001953 sensory effect Effects 0.000 description 1
- 210000002966 serum Anatomy 0.000 description 1
- 210000002832 shoulder Anatomy 0.000 description 1
- 231100000075 skin burn Toxicity 0.000 description 1
- 210000004927 skin cell Anatomy 0.000 description 1
- 201000002859 sleep apnea Diseases 0.000 description 1
- 210000000813 small intestine Anatomy 0.000 description 1
- 239000011734 sodium Substances 0.000 description 1
- 229910052708 sodium Inorganic materials 0.000 description 1
- 208000018198 spasticity Diseases 0.000 description 1
- 210000000952 spleen Anatomy 0.000 description 1
- 230000007480 spreading Effects 0.000 description 1
- 238000003892 spreading Methods 0.000 description 1
- 238000004659 sterilization and disinfection Methods 0.000 description 1
- 150000003431 steroids Chemical class 0.000 description 1
- 230000000475 sunscreen effect Effects 0.000 description 1
- 239000000516 sunscreening agent Substances 0.000 description 1
- 230000003319 supportive effect Effects 0.000 description 1
- 239000000829 suppository Substances 0.000 description 1
- 208000011580 syndromic disease Diseases 0.000 description 1
- 239000003826 tablet Substances 0.000 description 1
- 230000002936 tranquilizing effect Effects 0.000 description 1
- UFTFJSFQGQCHQW-UHFFFAOYSA-N triformin Chemical compound O=COCC(OC=O)COC=O UFTFJSFQGQCHQW-UHFFFAOYSA-N 0.000 description 1
- 230000002792 vascular Effects 0.000 description 1
- 230000002883 vasorelaxation effect Effects 0.000 description 1
- 235000019155 vitamin A Nutrition 0.000 description 1
- 239000011719 vitamin A Substances 0.000 description 1
- 235000019163 vitamin B12 Nutrition 0.000 description 1
- 239000011715 vitamin B12 Substances 0.000 description 1
- 150000003722 vitamin derivatives Chemical class 0.000 description 1
- 230000008673 vomiting Effects 0.000 description 1
- 239000011701 zinc Substances 0.000 description 1
- 229910052725 zinc Inorganic materials 0.000 description 1
- OENHQHLEOONYIE-JLTXGRSLSA-N β-Carotene Chemical compound CC=1CCCC(C)(C)C=1\C=C\C(\C)=C\C=C\C(\C)=C\C=C\C=C(/C)\C=C\C=C(/C)\C=C\C1=C(C)CCCC1(C)C OENHQHLEOONYIE-JLTXGRSLSA-N 0.000 description 1
Images
Classifications
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/12—Ketones
- A61K31/122—Ketones having the oxygen directly attached to a ring, e.g. quinones, vitamin K1, anthralin
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K9/00—Medicinal preparations characterised by special physical form
- A61K9/10—Dispersions; Emulsions
- A61K9/127—Liposomes
- A61K9/1277—Processes for preparing; Proliposomes
-
- A—HUMAN NECESSITIES
- A23—FOODS OR FOODSTUFFS; TREATMENT THEREOF, NOT COVERED BY OTHER CLASSES
- A23L—FOODS, FOODSTUFFS, OR NON-ALCOHOLIC BEVERAGES, NOT COVERED BY SUBCLASSES A21D OR A23B-A23J; THEIR PREPARATION OR TREATMENT, e.g. COOKING, MODIFICATION OF NUTRITIVE QUALITIES, PHYSICAL TREATMENT; PRESERVATION OF FOODS OR FOODSTUFFS, IN GENERAL
- A23L2/00—Non-alcoholic beverages; Dry compositions or concentrates therefor; Their preparation
- A23L2/52—Adding ingredients
- A23L2/56—Flavouring or bittering agents
-
- A—HUMAN NECESSITIES
- A23—FOODS OR FOODSTUFFS; TREATMENT THEREOF, NOT COVERED BY OTHER CLASSES
- A23L—FOODS, FOODSTUFFS, OR NON-ALCOHOLIC BEVERAGES, NOT COVERED BY SUBCLASSES A21D OR A23B-A23J; THEIR PREPARATION OR TREATMENT, e.g. COOKING, MODIFICATION OF NUTRITIVE QUALITIES, PHYSICAL TREATMENT; PRESERVATION OF FOODS OR FOODSTUFFS, IN GENERAL
- A23L2/00—Non-alcoholic beverages; Dry compositions or concentrates therefor; Their preparation
- A23L2/52—Adding ingredients
- A23L2/68—Acidifying substances
-
- A—HUMAN NECESSITIES
- A23—FOODS OR FOODSTUFFS; TREATMENT THEREOF, NOT COVERED BY OTHER CLASSES
- A23L—FOODS, FOODSTUFFS, OR NON-ALCOHOLIC BEVERAGES, NOT COVERED BY SUBCLASSES A21D OR A23B-A23J; THEIR PREPARATION OR TREATMENT, e.g. COOKING, MODIFICATION OF NUTRITIVE QUALITIES, PHYSICAL TREATMENT; PRESERVATION OF FOODS OR FOODSTUFFS, IN GENERAL
- A23L2/00—Non-alcoholic beverages; Dry compositions or concentrates therefor; Their preparation
- A23L2/70—Clarifying or fining of non-alcoholic beverages; Removing unwanted matter
- A23L2/72—Clarifying or fining of non-alcoholic beverages; Removing unwanted matter by filtration
-
- A—HUMAN NECESSITIES
- A23—FOODS OR FOODSTUFFS; TREATMENT THEREOF, NOT COVERED BY OTHER CLASSES
- A23L—FOODS, FOODSTUFFS, OR NON-ALCOHOLIC BEVERAGES, NOT COVERED BY SUBCLASSES A21D OR A23B-A23J; THEIR PREPARATION OR TREATMENT, e.g. COOKING, MODIFICATION OF NUTRITIVE QUALITIES, PHYSICAL TREATMENT; PRESERVATION OF FOODS OR FOODSTUFFS, IN GENERAL
- A23L2/00—Non-alcoholic beverages; Dry compositions or concentrates therefor; Their preparation
- A23L2/70—Clarifying or fining of non-alcoholic beverages; Removing unwanted matter
- A23L2/80—Clarifying or fining of non-alcoholic beverages; Removing unwanted matter by adsorption
-
- A—HUMAN NECESSITIES
- A23—FOODS OR FOODSTUFFS; TREATMENT THEREOF, NOT COVERED BY OTHER CLASSES
- A23L—FOODS, FOODSTUFFS, OR NON-ALCOHOLIC BEVERAGES, NOT COVERED BY SUBCLASSES A21D OR A23B-A23J; THEIR PREPARATION OR TREATMENT, e.g. COOKING, MODIFICATION OF NUTRITIVE QUALITIES, PHYSICAL TREATMENT; PRESERVATION OF FOODS OR FOODSTUFFS, IN GENERAL
- A23L3/00—Preservation of foods or foodstuffs, in general, e.g. pasteurising, sterilising, specially adapted for foods or foodstuffs
- A23L3/005—Preservation of foods or foodstuffs, in general, e.g. pasteurising, sterilising, specially adapted for foods or foodstuffs by heating using irradiation or electric treatment
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/045—Hydroxy compounds, e.g. alcohols; Salts thereof, e.g. alcoholates
- A61K31/05—Phenols
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/33—Heterocyclic compounds
- A61K31/335—Heterocyclic compounds having oxygen as the only ring hetero atom, e.g. fungichromin
- A61K31/35—Heterocyclic compounds having oxygen as the only ring hetero atom, e.g. fungichromin having six-membered rings with one oxygen as the only ring hetero atom
- A61K31/352—Heterocyclic compounds having oxygen as the only ring hetero atom, e.g. fungichromin having six-membered rings with one oxygen as the only ring hetero atom condensed with carbocyclic rings, e.g. methantheline
- A61K31/353—3,4-Dihydrobenzopyrans, e.g. chroman, catechin
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/70—Carbohydrates; Sugars; Derivatives thereof
- A61K31/715—Polysaccharides, i.e. having more than five saccharide radicals attached to each other by glycosidic linkages; Derivatives thereof, e.g. ethers, esters
- A61K31/726—Glycosaminoglycans, i.e. mucopolysaccharides
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K36/00—Medicinal preparations of undetermined constitution containing material from algae, lichens, fungi or plants, or derivatives thereof, e.g. traditional herbal medicines
- A61K36/18—Magnoliophyta (angiosperms)
- A61K36/185—Magnoliopsida (dicotyledons)
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K36/00—Medicinal preparations of undetermined constitution containing material from algae, lichens, fungi or plants, or derivatives thereof, e.g. traditional herbal medicines
- A61K36/18—Magnoliophyta (angiosperms)
- A61K36/88—Liliopsida (monocotyledons)
- A61K36/886—Aloeaceae (Aloe family), e.g. aloe vera
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K8/00—Cosmetics or similar toiletry preparations
- A61K8/02—Cosmetics or similar toiletry preparations characterised by special physical form
- A61K8/14—Liposomes; Vesicles
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K8/00—Cosmetics or similar toiletry preparations
- A61K8/18—Cosmetics or similar toiletry preparations characterised by the composition
- A61K8/96—Cosmetics or similar toiletry preparations characterised by the composition containing materials, or derivatives thereof of undetermined constitution
- A61K8/97—Cosmetics or similar toiletry preparations characterised by the composition containing materials, or derivatives thereof of undetermined constitution from algae, fungi, lichens or plants; from derivatives thereof
- A61K8/9783—Angiosperms [Magnoliophyta]
- A61K8/9794—Liliopsida [monocotyledons]
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K9/00—Medicinal preparations characterised by special physical form
- A61K9/0012—Galenical forms characterised by the site of application
- A61K9/0014—Skin, i.e. galenical aspects of topical compositions
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K9/00—Medicinal preparations characterised by special physical form
- A61K9/0012—Galenical forms characterised by the site of application
- A61K9/0053—Mouth and digestive tract, i.e. intraoral and peroral administration
- A61K9/0056—Mouth soluble or dispersible forms; Suckable, eatable, chewable coherent forms; Forms rapidly disintegrating in the mouth; Lozenges; Lollipops; Bite capsules; Baked products; Baits or other oral forms for animals
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K9/00—Medicinal preparations characterised by special physical form
- A61K9/0012—Galenical forms characterised by the site of application
- A61K9/0053—Mouth and digestive tract, i.e. intraoral and peroral administration
- A61K9/006—Oral mucosa, e.g. mucoadhesive forms, sublingual droplets; Buccal patches or films; Buccal sprays
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K9/00—Medicinal preparations characterised by special physical form
- A61K9/08—Solutions
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K9/00—Medicinal preparations characterised by special physical form
- A61K9/10—Dispersions; Emulsions
- A61K9/127—Liposomes
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61Q—SPECIFIC USE OF COSMETICS OR SIMILAR TOILETRY PREPARATIONS
- A61Q11/00—Preparations for care of the teeth, of the oral cavity or of dentures; Dentifrices, e.g. toothpastes; Mouth rinses
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61Q—SPECIFIC USE OF COSMETICS OR SIMILAR TOILETRY PREPARATIONS
- A61Q19/00—Preparations for care of the skin
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61Q—SPECIFIC USE OF COSMETICS OR SIMILAR TOILETRY PREPARATIONS
- A61Q19/00—Preparations for care of the skin
- A61Q19/08—Anti-ageing preparations
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61Q—SPECIFIC USE OF COSMETICS OR SIMILAR TOILETRY PREPARATIONS
- A61Q7/00—Preparations for affecting hair growth
-
- C—CHEMISTRY; METALLURGY
- C02—TREATMENT OF WATER, WASTE WATER, SEWAGE, OR SLUDGE
- C02F—TREATMENT OF WATER, WASTE WATER, SEWAGE, OR SLUDGE
- C02F1/00—Treatment of water, waste water, or sewage
- C02F1/001—Processes for the treatment of water whereby the filtration technique is of importance
-
- C—CHEMISTRY; METALLURGY
- C02—TREATMENT OF WATER, WASTE WATER, SEWAGE, OR SLUDGE
- C02F—TREATMENT OF WATER, WASTE WATER, SEWAGE, OR SLUDGE
- C02F1/00—Treatment of water, waste water, or sewage
- C02F1/28—Treatment of water, waste water, or sewage by sorption
- C02F1/283—Treatment of water, waste water, or sewage by sorption using coal, charred products, or inorganic mixtures containing them
-
- C—CHEMISTRY; METALLURGY
- C02—TREATMENT OF WATER, WASTE WATER, SEWAGE, OR SLUDGE
- C02F—TREATMENT OF WATER, WASTE WATER, SEWAGE, OR SLUDGE
- C02F1/00—Treatment of water, waste water, or sewage
- C02F1/30—Treatment of water, waste water, or sewage by irradiation
- C02F1/32—Treatment of water, waste water, or sewage by irradiation with ultraviolet light
- C02F1/325—Irradiation devices or lamp constructions
-
- C—CHEMISTRY; METALLURGY
- C02—TREATMENT OF WATER, WASTE WATER, SEWAGE, OR SLUDGE
- C02F—TREATMENT OF WATER, WASTE WATER, SEWAGE, OR SLUDGE
- C02F1/00—Treatment of water, waste water, or sewage
- C02F1/66—Treatment of water, waste water, or sewage by neutralisation; pH adjustment
-
- C—CHEMISTRY; METALLURGY
- C02—TREATMENT OF WATER, WASTE WATER, SEWAGE, OR SLUDGE
- C02F—TREATMENT OF WATER, WASTE WATER, SEWAGE, OR SLUDGE
- C02F1/00—Treatment of water, waste water, or sewage
- C02F1/68—Treatment of water, waste water, or sewage by addition of specified substances, e.g. trace elements, for ameliorating potable water
- C02F1/685—Devices for dosing the additives
-
- C—CHEMISTRY; METALLURGY
- C02—TREATMENT OF WATER, WASTE WATER, SEWAGE, OR SLUDGE
- C02F—TREATMENT OF WATER, WASTE WATER, SEWAGE, OR SLUDGE
- C02F1/00—Treatment of water, waste water, or sewage
- C02F1/68—Treatment of water, waste water, or sewage by addition of specified substances, e.g. trace elements, for ameliorating potable water
- C02F1/685—Devices for dosing the additives
- C02F1/686—Devices for dosing liquid additives
-
- A—HUMAN NECESSITIES
- A23—FOODS OR FOODSTUFFS; TREATMENT THEREOF, NOT COVERED BY OTHER CLASSES
- A23V—INDEXING SCHEME RELATING TO FOODS, FOODSTUFFS OR NON-ALCOHOLIC BEVERAGES AND LACTIC OR PROPIONIC ACID BACTERIA USED IN FOODSTUFFS OR FOOD PREPARATION
- A23V2002/00—Food compositions, function of food ingredients or processes for food or foodstuffs
-
- C—CHEMISTRY; METALLURGY
- C02—TREATMENT OF WATER, WASTE WATER, SEWAGE, OR SLUDGE
- C02F—TREATMENT OF WATER, WASTE WATER, SEWAGE, OR SLUDGE
- C02F2101/00—Nature of the contaminant
- C02F2101/10—Inorganic compounds
- C02F2101/12—Halogens or halogen-containing compounds
-
- C—CHEMISTRY; METALLURGY
- C02—TREATMENT OF WATER, WASTE WATER, SEWAGE, OR SLUDGE
- C02F—TREATMENT OF WATER, WASTE WATER, SEWAGE, OR SLUDGE
- C02F2103/00—Nature of the water, waste water, sewage or sludge to be treated
- C02F2103/32—Nature of the water, waste water, sewage or sludge to be treated from the food or foodstuff industry, e.g. brewery waste waters
-
- C—CHEMISTRY; METALLURGY
- C02—TREATMENT OF WATER, WASTE WATER, SEWAGE, OR SLUDGE
- C02F—TREATMENT OF WATER, WASTE WATER, SEWAGE, OR SLUDGE
- C02F2303/00—Specific treatment goals
- C02F2303/04—Disinfection
-
- C—CHEMISTRY; METALLURGY
- C02—TREATMENT OF WATER, WASTE WATER, SEWAGE, OR SLUDGE
- C02F—TREATMENT OF WATER, WASTE WATER, SEWAGE, OR SLUDGE
- C02F2303/00—Specific treatment goals
- C02F2303/16—Regeneration of sorbents, filters
-
- C—CHEMISTRY; METALLURGY
- C02—TREATMENT OF WATER, WASTE WATER, SEWAGE, OR SLUDGE
- C02F—TREATMENT OF WATER, WASTE WATER, SEWAGE, OR SLUDGE
- C02F2303/00—Specific treatment goals
- C02F2303/18—Removal of treatment agents after treatment
- C02F2303/185—The treatment agent being halogen or a halogenated compound
Definitions
- Delivery methods of medically beneficial products can a difference in whether a person will take the medically beneficial products. How the medically beneficial products ingredients are prepared affects the forms of delivery available to make the person consuming the medically beneficial products and can affect the potency and medical benefit efficacy.
- FIG. 1A shows for illustrative purposes only an example of a method and devices for cellular transfer of compounds with augmented reality application of one embodiment.
- FIG. 1B shows for illustrative purposes only an example of a liposome lipid chemical structure of one embodiment.
- FIG. 2A shows for illustrative purposes only an example of a liposome encapsulated CBD compound of one embodiment.
- FIG. 2B shows for illustrative purposes only an example of a liposome encapsulated Aloe Vera compound of one embodiment.
- FIG. 2C shows for illustrative purposes only an example of a liposome encapsulated Inflacin compound of one embodiment.
- FIG. 2D shows for illustrative purposes only an example of liposome encapsulated CBD, Aloe Vera, and Inflacin compounds of one embodiment.
- FIG. 3A shows for illustrative purposes only an example of a chemical structure of Aloe Vera compound emodin of one embodiment.
- FIG. 3B shows for illustrative purposes only an example of a chemical structure of Aloe Vera compound aleosin of one embodiment.
- FIG. 3C shows for illustrative purposes only an example of a chemical structure of Aloe Vera compound acemannan of one embodiment.
- FIG. 4A shows for illustrative purposes only an example of a chemical structure of CBD of one embodiment.
- FIG. 4B shows for illustrative purposes only an example of a chemical structure of THC of one embodiment.
- FIG. 5A shows for illustrative purposes only an example of a liposome 3D structure of one embodiment.
- FIG. 5B shows for illustrative purposes only an example of a liposome encapsulated molecule of one embodiment.
- FIG. 6 shows a block diagram of an overview of a liposome delivery system of combined Aloe Vera components and cannabis components of one embodiment.
- FIG. 7 shows for illustrative purposes only an example of a liposome attaching to human cell and both opening for transfer of Aloe Vera and CBD into the human cell of one embodiment.
- FIG. 8 shows a block diagram of an overview of examples of liposome cannabis product benefits of one embodiment.
- FIG. 9 shows a block diagram of an overview of continuation of examples of liposome cannabis product benefits of one embodiment.
- FIG. 10 shows a block diagram of an overview of examples of cannabinoid component product benefits of one embodiment.
- FIG. 11 shows a block diagram of an overview of examples of CBD component product benefits of one embodiment.
- FIG. 12 shows a block diagram of an overview of examples of Aloe Vera component product benefits of one embodiment.
- FIG. 13 shows for illustrative purposes only an example of nano sensors suspended in an encapsulation delivery application of one embodiment.
- FIG. 14 shows for illustrative purposes only an example of liposome delivery system cellular transfer into a user's skin of one embodiment.
- FIG. 15 shows for illustrative purposes only an example of a cellular transfer augmented reality application previewing treatment potential results of one embodiment.
- FIG. 16 shows for illustrative purposes only an example of a liposome lipid processing devices for encapsulating compounds and creating application delivery products of one embodiment.
- the method and devices for cellular transfer of compounds with augmented reality application can be configured using a combination of CBD and Aloe Vera.
- the method and devices for cellular transfer of compounds with augmented reality application can be configured to include only encapsulated CBD molecules and can be configured to include only encapsulated Aloe Vera molecules using the present invention.
- FIG. 1A shows for illustrative purposes only an example of a method and devices for cellular transfer of compounds with augmented reality application of one embodiment.
- FIG. 1A shows a bilayer liposome 100 .
- the bilayer liposome 100 is shown in a 2D illustration encapsulating CBD molecules 110 and Aloe Vera molecules 120 .
- the spherical liposome shape is formed by the hydrophobic tail 130 and hydrophilic head 140 of its compounds in an aqueous solution 150 .
- Cannabinoid compounds including the CBD molecules 110 and Aloe Vera molecules 120 are suspended in the aqueous solution 150 and encapsulated while the liposome is forming of one embodiment.
- FIG. 1A shows a liposome encapsulation of CBD and Aloe Vera molecules in combination.
- the liposome encapsulation may be used to encapsulate CBD molecules alone and Aloe Vera molecules alone.
- Separate liposome encapsulation of the two ingredients provides a method in which the proportioning of the separated CBD and Aloe Vera liposome encapsulations may be used to increase the health benefits of each for a specific purpose for a specific medical condition.
- a treatment product that is targeted for persons suffering from depression may receive the benefits of CBD constituents that treat depression in a larger proportion than Aloe Vera constituents that treat depression based on studies on the efficacy of the different constituents for the treatment of depression of one embodiment.
- a device may be used for blending varying proportions of separately encapsulated cannabinoid compound molecules and Aloe Vera molecules for increasing health benefits of each for a specific purpose for a specific medical condition.
- the device may be coupled to a digital server, a plurality of databases and a computer.
- the plurality of databases have recorded and stored data on varying proportional formulations of cannabinoid compound molecules and Aloe Vera molecules and their benefits for various medical conditions.
- the computer is used for querying the database for a specific medical condition and the cannabinoid and Aloe Vera constituent benefits.
- the digital server is used to instruct the blending device to blend with the liposome lipid in an aqueous solution proportional quantities of the various constituents using the varying proportional formulations of cannabinoid compound molecules and Aloe Vera molecules for blending a beneficial product and delivery system for a human to use for treatment of the specific medical condition of one embodiment.
- FIG. 1B shows for illustrative purposes only an example of a liposome lipid chemical structure of one embodiment.
- FIG. 1B shows an example of one lipid chemical structure 160 .
- the liposomes may be made of other lipid chemical structures of lipid compounds used for creating lipid 170 liposomes.
- the liposomes created from the lipid compounds and methods are characterized by the ability to inhibit biological activity, open readily due to a change in pH, may open readily due to a change in photo intensity and other characteristics that facilitate the delivery of the encapsulated molecules of one embodiment.
- FIG. 2A shows for illustrative purposes only an example of a liposome encapsulated CBD compound of one embodiment.
- FIG. 2A shows the bilayer liposome 100 in a 2D illustration encapsulating CBD molecules 110 .
- the bilayer liposome 100 encapsulated CBD molecules 110 form a base for a delivery system for products for consumption by humans.
- CBD provides a variety of benefits.
- Some of the benefits include treating anorexia, cachexia, gastrointestinal disorders, and nausea, appetite loss, control diabetes, treat Crohn's symptoms, Mood/behavior conditions, depression, Anxiety, control ADD/ADHD, stress, bipolar, OCD, PTSD, treating asthma, fatigue, hypertension, glaucoma, HIV/Aids, muscular dystrophy, providing relief from cancer and cancer treatment symptoms of one embodiment
- FIG. 2B shows for illustrative purposes only an example of a liposome encapsulated Aloe Vera compound of one embodiment.
- FIG. 2B shows the bilayer liposome 100 in a 2D illustration encapsulating Aloe Vera molecules 120 .
- the bilayer liposome 100 encapsulated Aloe Vera molecules 120 form a base for a delivery system for products for consumption by humans.
- Aloe vera is a rich source of over 200 naturally occurring nutrients which contain water soluble and fat soluble vitamins, minerals, enzymes, polysaccharides, phenolic compounds and organic acids. Its secondary metabolites have multiple properties such as anti-inflammatory, antibacterial, antioxidant, immune boosting, anticancer, antiaging, sunburn relief and antidiabetic potentials. Several traditional uses also have been reported such as burn injury, eczema, cosmetics, inflammation, and fever.
- Nine categories of phytochemical constituents of Aloe vera can be classified as, anthraquinones, inorganic compounds, amino acids, fatty acids, alkaloids, carbohydrates, enzymes, and vitamins along with other miscellaneous compounds.
- Aloe vera contains 75 potentially active constituents: vitamins, enzymes, minerals, sugars, lignin, saponins, salicylic acids and amino acids.
- Aloe vera vitamins include vitamins A (beta-carotene), C and E, which are antioxidants and vitamin B12, folic acid, and choline.
- Aloe vera enzymes include aliiase, alkaline phosphatase, amylase, bradykinase, carboxypeptidase, catalase, cellulase, lipase, and peroxidase. Bradykinase helps to reduce excessive inflammation when applied to the skin topically, while others help in the breakdown of sugars and fats.
- Aloe vera minerals include calcium, chromium, copper, selenium, magnesium, manganese, potassium, sodium and zinc.
- Aloe vera sugars include monosaccharides (glucose and fructose) and polysaccharides (glucomannans/polymannose). These are derived from the mucilage layer of the plant and are known as mucopolysaccharides. The most prominent monosaccharide is mannose-6-phosphate, and the most common polysaccharides are called glucomannans [beta-(1,4)-acetylated mannan]. Acemannan, a prominent glucomannan has also been found.
- a glycoprotein with antiallergic properties, called alprogen and novel anti-inflammatory compound, C-glucosyl chromone has been isolated from Aloe vera gel.
- Aloe vera anthraquinones include phenolic compounds traditionally known as laxatives and Aloin and emodin act as analgesics, antibacterials and antivirals.
- Aloe vera fatty acids include 4 plant steroids; cholesterol, campesterol, ⁇ -sisosterol and lupeol. All these have anti-inflammatory action and lupeol also possesses antiseptic and analgesic properties.
- Aloe vera hormones include auxins and gibberellins that help in wound healing and have anti-inflammatory action.
- Aloe vera other potentially active constituents include 20 of the 22 human required amino acids and 7 of the 8 essential amino acids. It also contains salicylic acid that possesses anti-inflammatory and antibacterial properties.
- Lignin an inert substance, when included in topical preparations, enhances penetrative effect of the other ingredients into the skin. Saponins that are the soapy substances form about 3% of the gel and have cleansing and antiseptic properties.
- Aloe Vera One example of the benefits of Aloe Vera is found in the use of Aloe Vera juice mixed with water and honey used as an effective antimalarial cure in Iraq. There are many other reported and studied uses and benefits throughout the world of one embodiment.
- Aloe Vera phytochemical constituents of anthraquinones as one of the most important active ingredients of Aloe Vera.
- the antiplasmodial activity of Aloe Vera may be explained in the light of the presence of anthraquinones and other quinoid compounds which exert good activity against P. falciparum .
- the four main anthraquinones showing quite high medical values are acemannan, aloe-emodin, aloe bitter and aloe lectin of one embodiment.
- FIG. 2C shows for illustrative purposes only an example of a liposome encapsulated Inflacin compound of one embodiment.
- FIG. 2C shows the bilayer liposome 100 in a 2D illustration encapsulating Inflacin molecules 200 .
- the bilayer liposome 100 encapsulated Inflacin molecules 200 form a base for a delivery system for products for consumption by humans.
- a group of compounds called Inflacin may be topically applied to alleviate pain associated with arthritis and increased joint mobility.
- Inflacin provides its analgesic benefit when applying the topical cream to areas of the body affected by stiffness, soreness and pain. These include: hands, feet, knees and shoulders and muscles of the neck, arms, legs and back.
- liposome encapsulated Inflacin in for example a topical cream delivers rapid absorption through the skin cells to deliver pain relief and increased mobility for example hand gripping within minutes of one embodiment.
- FIG. 2D shows for illustrative purposes only an example of liposome encapsulated CBD, Aloe Vera, and Inflacin compounds of one embodiment.
- FIG. 2D shows the bilayer liposome 100 in a 2D illustration encapsulating CBD molecules 110 , Aloe Vera molecules 120 , and Inflacin molecules 200 . These three compounds may be included in the liposome encapsulation process singularly, or in any combination of two or all three as shown.
- the liposome encapsulation process may also include other compounds for example other cannabinoids for targeting specific medical benefits for specific conditions and symptoms of one embodiment.
- FIG. 3A shows for illustrative purposes only an example of a chemical structure of Aloe Vera compound emodin of one embodiment.
- FIG. 3A shows a chemical structure of Aloe Vera compound emodin 300 .
- An emodin 302 molecule as shown in the chemical structure of Aloe Vera compound emodin 300 contains anthraquinones that generate reactive oxygen and thus inactivate malaria parasites.
- Emodin 302 also provides beneficial properties for immunity and inflammation, antioxidant property, inflammatory bowel disease, supportive care of heart failure/function, hypertension and related disorders, diabetes mellitus, aging-related neurological diseases, atopic dermatitis, hepatic inflammation, autoimmune disorders including rheumatoid arthritis and autoimmune diabetes mellitus, renal inflammatory conditions, and infectious diseases of one embodiment.
- FIG. 3B shows for illustrative purposes only an example of a chemical structure of Aloe Vera compound aleosin of one embodiment.
- FIG. 3B shows a chemical structure of Aloe Vera compound aleosin 310 .
- An aleosin 312 molecule as shown in the chemical structure of Aloe Vera compound aleosin 310 and is an active constituent of the herb Aloe Vera.
- Aloesin suppresses cell growth and metastasis in ovarian cancer SKOV3 cells through the Inhibition of the MAPK Signaling Pathway, and plays a crucial role in anti-inflammatory activity, ultraviolet protection, and antibacterium.
- Aloesin accelerates skin wound healing by modulating MAPK/Rho and Smad signaling pathways, has antioxidant properties, provides a significant beneficial effect in lowering blood glucose and improving insulin resistance in humans, and the activity of aloesin increases adiponectin production and improves the insulin sensitivity of one embodiment.
- FIG. 3C shows for illustrative purposes only an example of a chemical structure of Aloe Vera compound acemannan of one embodiment.
- FIG. 3C shows a chemical structure of Aloe Vera compound acemannan 320 .
- Acemannan 322 is found in the Aloe Vera plant.
- Acemannan 322 has various properties and benefits including helps cells to be more resistant to viruses and pathogenic bacteria, improves overall cellular metabolism and functioning, promotes healthy inflammation response, provides critical lubrication of joints, aids in the absorption of water, minerals, and nutrients in the GI tract, reduces pain, improves vascular flow, reduces scarring, increases the body's own production of interferon, interleukins, increase the number of antibody forming T-cells in the spleen, increases the number and activity of killer T-cell and increase monocyte activity, soothes and promotes healing of intestinal disorders such as indigestion, heartburn, hyper-acidity, peptic and duodenal ulcers, colitis, and hemorrhoids, promotes healthy kidney function, speeds wound healing, reduces allergic reactions, stimulates bone marrow activity, anti-aging properties, and supports healthy blood pressure of one embodiment.
- FIG. 4A shows for illustrative purposes only an example of a chemical structure of CBD of one embodiment.
- FIG. 4A shows a chemical structure of CBD 400 with a molecular name of cannabidiol (CBD) 410 .
- CBD cannabidiol
- the illustration shows a hydroxyl group 420 bonded to one of a group of carbon atom cyclic rings that create the bonds for the branch and chain structures of one embodiment.
- FIG. 4B shows for illustrative purposes only an example of a chemical structure of THC of one embodiment.
- FIG. 4B shows a chemical structure of THC 430 .
- This chemical structure of THC 430 has a molecular name of tetrahydrocannabinol (THC) 440 .
- the illustration shows the carbon atom cyclic ring 450 structures that create the branch bonds.
- THC 430 is not a legal compound federally. Its use may only be legal in States and only within that State that has legalized its use. Therefore the embodiments of this invention may exclude the addition of THC 430 where it is not legal without changing the method or non-THC embodiments.
- CBD derived from hemp is federally legal.
- CBD may also be derived from non-hemp cannabis plants and must meet minimum THC 430 levels to be used for interstate purposes of one embodiment.
- FIG. 5A shows for illustrative purposes only an example of a liposome 3D structure of one embodiment.
- FIG. 5A shows a liposome 3D structure 500 .
- the liposome 3D structure 500 is formed during a liposome CBD-Aloe Vera process cell disruption operation.
- FIG. 5A shows an internal aqueous compartment 510 is created when the hydrophobic tail 130 and hydrophilic head 140 elements of lipid materials are aligned during the cell disruption operation.
- the liposome 3D structure 500 can be seen to be spherical.
- the hydrophobic tail 130 and hydrophilic head 140 alignments also form bonds between the hydrophilic head 140 elements and the hydrophobic and hydrophilic attractions and repulsions cause the spherical associations of the lipid elements of one embodiment.
- FIG. 5B shows for illustrative purposes only an example of a liposome encapsulated molecule of one embodiment.
- FIG. 5B shows the liposome 3D structure 500 .
- the liposome 3D structure 500 forms a bilayer vesicle with an internal void.
- the liposome CBD-Aloe Vera process suspends molecules of a component in an aqueous solution as illustrated by a liposome encapsulated molecule 520 .
- the suspended molecule fills the internal void during cell disruption and becomes encapsulated as the liposome completes the formation of the bilayer vesicle of one embodiment.
- FIG. 6 shows a block diagram of an overview of a liposome delivery system of combined Aloe Vera components and cannabis components of one embodiment.
- FIG. 6 shows a liposome delivery system of Aloe Vera components 600 emodin 302 , aloesin 312 and acemannan 322 .
- a liposome delivery system of combined Aloe Vera components and cannabis components 610 including emodin 302 , aloesin 312 , acemannan 322 , CBD 400 and THC 430 .
- Other liposome delivery system components including lanolin, retinol, vitamin e, anti-wrinkle creams and treatments for transporting liposome encapsulated ingredients 625 .
- Aloe Vera components and cannabis components can be formulated as any of the components alone or in various combinations of components from each group of Aloe Vera components and cannabis components.
- the products for oral sublingual ingestion and nasal spray, and suppository insertion and tampon vaginal insertion 630 or topical applications including underarm topical application 640 may be formulated for targeting specific medical benefits for specific conditions and symptoms.
- Aloe Vera has anti-inflammatory properties 1237 and cannabis components of a combined group of CBC, CBD, CBDA, CBG, CBN, THC, THCA 925 relieves and reduces arthritis, inflammation 935 .
- a liposome delivery system may include products for oral sublingual ingestion and nasal spray, and suppository insertion and tampon vaginal insertion 630 or topical applications including underarm topical application 640 .
- Liposome delivery system products for oral including sublingual ingestion and nasal spray may include at least one of a group beverages, flavored beverages, pills, capsules, tablets and sprays and for suppository insertion include rectal suppositories used by humans.
- Liposome delivery system products for topical applications including underarm topical application 640 include at least one of a group of forms including creams, gels, ointments, salves, sprays, powders, serums, liquids, toners, and oils for use in cosmetics, first aid, and sunscreens by humans.
- a liposome delivery system in topical applications including underarm topical application 640 may be formulated with these combined Aloe Vera and cannabis components to target arthritic inflammation where a topical cream is formed for applying to a person's hands that are suffering from arthritis of one embodiment.
- FIG. 7 shows for illustrative purposes only an example of a liposome attaching to human cell and both opening for transfer of Aloe Vera and CBD into the human cell of one embodiment.
- FIG. 7 shows a liposome encapsulated Aloe Vera and CBD 700 liposome attached to a human cell.
- FIG. 7 shows a liposome attaching to a human cell and both bilayer structures opening for transfer of Aloe Vera and CBD into the human cell 730 .
- a human cell membrane is composed of a lipid bilayer structure. The human cell membrane lipid molecules each have a hydrophilic and a hydrophobic end. Rapid absorption occurs with the liposome bilayer spreading over a human cell.
- the liposome encapsulating bilayer structure 710 begins to breach as does the human cell 720 membrane upon contact.
- the liposome bilayer with the encapsulated material reacts with the human cell membrane bilayer wherein the hydrophobic characteristic of the hydrophobic tail grouping creates a breach in the human cell membrane.
- the encapsulated material passes through the breach into the human cell and the human cell material passes through the breach into newly created voids of the vesicle interior filling the void left by the passing encapsulated material thereby accelerating the rate of the transfer of substances.
- the bilayer collapses across the surface of the human cell membrane resealing the human cell membrane and the excess bilayer material is absorbed and excreted through normal bodily functions of one embodiment.
- FIG. 8 shows a block diagram of an overview of examples of liposome cannabis product benefits of one embodiment.
- FIG. 8 shows examples of liposome cannabis product benefits 800 in different groupings of medical conditions and symptoms. For example conditions related to gastrointestinal 810 involvements.
- a combination of cannabis product components CBD, THC 820 is used to treat anorexia, cachexia, gastrointestinal disorders, and nausea 830 .
- CBN, THC 822 reduces appetite loss 832 .
- a combination of CBD, THCV 824 helps control diabetes 834 .
- CBD, THC 826 is used to treat Crohn's 836 symptoms of one embodiment.
- Mood/behavior 840 conditions are treated using a combination of CBC, CBD, CBG, CBN, and THC 850 for depression 860 .
- CBD, CBG 852 is used to treat anxiety 862 .
- CBD, THC 854 helps control ADD/ADHD, stress 864 , attention deficit disorder (ADD) and attention deficit hyperactivity disorder (ADHD).
- the combination of CBD, CBG, and THC 856 is used to treat bipolar, OCD, PTSD 866 , obsessive-compulsive disorder (OCD) and post-traumatic stress disorder (PTSD) of one embodiment.
- Other 870 conditions and symptoms include the use of CBD, THC 880 for treating asthma, fatigue, hypertension 890 , and CBG, THC 881 for glaucoma 891 .
- Treatments with CBC, CBD, CBG, and THC 883 are beneficial for muscular dystrophy 893 .
- the liposome cannabis product combination of components CBC, CBD, CBDA, CBG, THC, and THCA 884 is used for providing relief from cancer 894 and cancer treatment symptoms of one embodiment. The benefits are further described in FIG. 9 .
- FIG. 9 shows a block diagram of an overview of continuation of examples of liposome cannabis product benefits of one embodiment.
- FIG. 9 shows continuing from FIG. 8 a continuation of examples of liposome cannabis product benefits 900 .
- Medical conditions that affect pain/sleep 910 can benefit from combinations of cannabis product components for example CBD, THC 920 for treating sleep apnea 930 ; CBD, THC 921 for reduced cramps, migraine/headache, phantom limb, spinal injury 931 .
- CBD, CBN, THC 922 is used to treat fibromyalgia 932 .
- CBC, CBD, CBN, THC 923 provides relief for insomnia 933 .
- the combination of CBC, CBD, CBN, THC, and THCV 924 reduces pain 934 .
- the combined group of CBC, CBD, CBDA, CBG, CBN, THC, and THCA 925 relieves and reduces arthritis, inflammation 935 .
- Neurological 940 conditions are treated using liposome combinations of cannabis product components.
- CBD, THC 950 is used to treat Tourette's 960 syndrome symptoms.
- CBD, CBN, THCA, THCV 951 help control epilepsy, seizures 961 onsets.
- CBCD, CBN, THC, THCA 952 is used to treat the symptoms of multiple sclerosis 962 .
- CBC, CBD, CBG, THC, and THCA 953 is used to treat Alzheimer's, Parkinson's 963 .
- CBD, CBG, CBN, THC, THCA 954 reduces spasticity 964 .
- CBC, CBD, CBG, CBN, THCV 955 benefit osteoporosis 965 effects.
- CBC, CBD, CBG, CBN, THC, THCA 956 is used to treat ALS 966 , Amyotrophic lateral sclerosis (ALS), also known as Lou Gehrig's disease of one embodiment.
- ALS Amyotrophic lateral sclerosis
- FIG. 10 shows a block diagram of an overview of examples of cannabinoid component product benefits of one embodiment.
- FIG. 10 shows examples of cannabinoid component product benefits 1000 .
- CBDA 1001 is a cannabinoid component that reduces inflammation 1002 and inhibits cancer cell growth 1003 .
- CBG 1030 is a cannabinoid component that aids sleep 1031 , inhibits cancer cell growth 1032 , and promotes bone growth 1033 .
- Another cannabinoid component is CBGA 1010 that reduces inflammation 1011 , relieves pain 1012 , and slows bacterial growth 1013 .
- CBC 1040 with properties that inhibits cancer cell growth 1041 , promotes bone growth 1042 , reduces inflammation 1043 , and relieves pain 1044 .
- One of the cannabinoid components is CBCA 1020 that reduces inflammation 1021 and treats fungal infection 1022 .
- Still another one of the group of cannabinoid components is CBN 1050 that reduces inflammation 1051 , relieves pain 1052 , aids sleep 1053 , is an appetite stimulant 1054 , and is an anti-convulsive 1055 of one embodiment.
- FIG. 11 shows a block diagram of an overview of examples of CBD component product benefits of one embodiment.
- FIG. 11 shows examples of CBD component product benefits 1100 .
- CBD 1110 benefits include properties that promotes function in the immune system 1120 , reduces small intestine contractions 1121 , reduces vomiting and nausea 1122 , suppresses muscle spasms 1123 , vasorelaxant 1124 , tranquillizing 1125 , relieves pain 1126 , relieves anxiety 1127 , treats psoriasis 1128 , reduces inflammation 1130 , reduces seizures and convulsions 1131 , reduces risk of artery blockage 1132 , reduces blood sugar levels 1133 , inhibits cancer cell growth 1134 , promotes bone growth 1135 , slows bacterial growth 1136 , neuro-protective 1137 , and antibacterial 1138 of one embodiment.
- FIG. 12 shows a block diagram of an overview of examples of Aloe Vera component product benefits of one embodiment.
- FIG. 12 shows examples of Aloe Vera component product benefits 1200 .
- Aloe vera 1210 is a succulent has been used for health purposes, dating back to ancient Egypt. The Aloe vera 1210 plant is grown in tropical climates worldwide. It is known for relieving heartburn to potentially slowing the spread of breast cancer, researchers are just beginning to unlock the benefits of this universal plant and its many byproducts.
- Aloe vera 1210 has benefits that include antioxidant and antibacterial properties 1220 , lowers the triglyceride levels among people with type 2 diabetes 1221 , accelerates the healing of burns 1222 , reduces dental plaque 1223 , improve skin and prevent wrinkles 1224 , lowers blood sugar levels in diabetics 1225 , reduce hair loss 1226 , relieve psoriatic arthritis symptoms 1230 , treat acne lesions 1231 , keeping skin hydrated and clear 1232 , treat skin burns 1233 , reduce itchiness and inflammation 1234 , a pain reliever salicylic acid found in Aloe Vera 1235 , treat hemorrhoids 1236 , and anti-inflammatory properties 1237 of one embodiment.
- FIG. 13 shows for illustrative purposes only an example of nano sensors suspended in an encapsulation delivery application of one embodiment.
- FIG. 13 shows a plurality of nano sensors 1300 suspended in delivery application 1310 of a liposome encapsulation of CBD molecules 110 and Aloe Vera molecules 120 in a bilayer liposome 100 .
- the plurality of nano sensors 1300 will be included in a liposome encapsulation of compounds delivery application media 1320 for example a cream for external delivery of the encapsulated compounds for example topical creams.
- the plurality of nano sensors 1300 may include temperature sensors, chemical analyzing sensors and other sensors to determine the biological conditions in the cells.
- the plurality of nano sensors 1300 may be read using an external device.
- the external device may include a user digital device with a cellular transfer augmented reality application installed.
- the external device will receive and process the data gathering results of the plurality of nano sensors 1300 determinations and prepare a digital and printed report for a user's physician's evaluation for one embodiment.
- FIG. 14 shows for illustrative purposes only an example of liposome delivery system cellular transfer into a user's skin of one embodiment.
- FIG. 14 shows a user with forehead wrinkles 1400 .
- the user has applied a topical application of the liposome delivery system cellular transfer compounds.
- An initial liposome opening to transfer compounds into user cells 1410 takes place open application to the user's skin.
- a 3d depth camera 1420 is used for capturing images of user's forehead 1425 . After the initial period of time wrinkles are beginning to fade 1430 . Liposome released compounds are penetrating deeper into the user's skin 1440 .
- the 3d depth camera 1420 is capturing images of wrinkles beginning to fade 1455 .
- the 3d depth camera 1420 has been capturing images of the significantly faded wrinkles on the user's forehead 1485 .
- the user's application of the topical cream of the liposome delivery system cellular transfer compounds has quickly and effectively reduced the user's forehead wrinkles of one embodiment.
- FIG. 15 shows for illustrative purposes only an example of a cellular transfer augmented reality application previewing treatment potential results of one embodiment.
- FIG. 15 shows a cellular transfer network 1500 including a digital server 1510 , plurality of databases 1520 , a cellular transfer augmented reality application 1530 installed on a cellular transfer network computer 1540 and an artificial intelligence 1550 module.
- a user may connect to the cellular transfer network 1500 via the internet 1560 using a user's digital device with depth camera 1570 with the cellular transfer augmented reality application 1530 installed.
- the user with forehead wrinkles 1400 can use the depth camera to provide a “before” 3D photograph of the wrinkles.
- the cellular transfer network 1500 artificial intelligence 1550 module can produce an Augmented Reality (AR) 3D preview for the user to allow the user to see at least an average result using data stored on the plurality of databases 1520 .
- Augmented Reality (AR) is a live, direct or indirect view of a physical, real-world environment whose elements are augmented (or supplemented) by computer-generated sensory input such as sound, video, graphics or GPS data. In this instance the user will see the progress of the wrinkles fading in real time after the application of the topical cream with the liposome delivery system cellular transfer compounds. The user is made aware that their results may differ but based on their physical conditions input this is the possible outcome of one embodiment.
- FIG. 16 shows for illustrative purposes only an example of a liposome lipid processing devices for encapsulating compounds and creating application delivery products of one embodiment.
- FIG. 16 shows the cellular transfer network 1500 , digital server 1510 , plurality of data bases 1520 , cellular transfer augmented reality application 1530 and cellular transfer network computer 1540 controlling the production of the lipid liposome encapsulation process and additional processing to create the application delivery products.
- the artificial intelligence cloud 1610 monitoring the processing conditions including temperatures, ingredient proportioning to the volume of liposome volume and can adjust those factors to produce a predetermine formulation of the products.
- cellular transfer network 1500 processes controls 1620 are connected to the processing devices using a processes controls interface 1630 .
- a container sterilization processor 1632 For example the temperature of a container sterilization processor 1632 is adjusted for the predetermined container type and materials to prevent damaging the container.
- a phospholipids supply tank 1640 , CBD supply tank 1642 for example and an Aloe Vera supply tank 1644 for example are shown to convey those compounds into the pre-disrupting liposome combination chamber 1650 .
- Disrupting processes 1660 create the conditions for the formation of the liposomes and encapsulation of the compounds in this illustration CBD and Aloe Vera.
- a production line will include for example a beverage liquid or topical cream supply tank 1646 .
- a sterilizing mixing tank 1665 is used to blend the liposome encapsulated compounds with the product delivery ingredient.
- a mixture temperature controller and filling pump with digital valve 1670 measures the filling of the beverage containers or topical cream pump containers 1672 and upon completion initiates a container capping processor 1674 . After capping the containers are processed for packaging 1680 of one embodiment.
Landscapes
- Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Veterinary Medicine (AREA)
- Public Health (AREA)
- General Health & Medical Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- Epidemiology (AREA)
- Medicinal Chemistry (AREA)
- Pharmacology & Pharmacy (AREA)
- Engineering & Computer Science (AREA)
- Nutrition Science (AREA)
- Dermatology (AREA)
- Environmental & Geological Engineering (AREA)
- Organic Chemistry (AREA)
- Hydrology & Water Resources (AREA)
- Water Supply & Treatment (AREA)
- Natural Medicines & Medicinal Plants (AREA)
- Polymers & Plastics (AREA)
- Food Science & Technology (AREA)
- Birds (AREA)
- Botany (AREA)
- Biotechnology (AREA)
- Microbiology (AREA)
- Mycology (AREA)
- Dispersion Chemistry (AREA)
- Molecular Biology (AREA)
- Gerontology & Geriatric Medicine (AREA)
- Alternative & Traditional Medicine (AREA)
- Medical Informatics (AREA)
- Physiology (AREA)
- Toxicology (AREA)
- Zoology (AREA)
- Oral & Maxillofacial Surgery (AREA)
- Medicinal Preparation (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Physical Water Treatments (AREA)
Abstract
The embodiments disclose a method, including suspending cannabinoid compound molecules and constituents in an aqueous solution, suspending Aloe Vera molecules and its constituents in an aqueous solution, wherein a combination of cannabinoid compound molecules and constituents and Aloe Vera molecules and its constituents may be used for suspending in an aqueous solution, encapsulating cannabinoid compound molecules and Aloe Vera molecules within a liposome in an aqueous solution, and blending the liposome encapsulated cannabinoid compound molecules and Aloe Vera molecules with other ingredients into a health beneficial product and delivery system for oral including sublingual ingestion and nasal spray and suppository insertion or topical application with a plurality of nano sensors by humans.
Description
- Delivery methods of medically beneficial products can a difference in whether a person will take the medically beneficial products. How the medically beneficial products ingredients are prepared affects the forms of delivery available to make the person consuming the medically beneficial products and can affect the potency and medical benefit efficacy.
-
FIG. 1A shows for illustrative purposes only an example of a method and devices for cellular transfer of compounds with augmented reality application of one embodiment. -
FIG. 1B shows for illustrative purposes only an example of a liposome lipid chemical structure of one embodiment. -
FIG. 2A shows for illustrative purposes only an example of a liposome encapsulated CBD compound of one embodiment. -
FIG. 2B shows for illustrative purposes only an example of a liposome encapsulated Aloe Vera compound of one embodiment. -
FIG. 2C shows for illustrative purposes only an example of a liposome encapsulated Inflacin compound of one embodiment. -
FIG. 2D shows for illustrative purposes only an example of liposome encapsulated CBD, Aloe Vera, and Inflacin compounds of one embodiment. -
FIG. 3A shows for illustrative purposes only an example of a chemical structure of Aloe Vera compound emodin of one embodiment. -
FIG. 3B shows for illustrative purposes only an example of a chemical structure of Aloe Vera compound aleosin of one embodiment. -
FIG. 3C shows for illustrative purposes only an example of a chemical structure of Aloe Vera compound acemannan of one embodiment. -
FIG. 4A shows for illustrative purposes only an example of a chemical structure of CBD of one embodiment. -
FIG. 4B shows for illustrative purposes only an example of a chemical structure of THC of one embodiment. -
FIG. 5A shows for illustrative purposes only an example of aliposome 3D structure of one embodiment. -
FIG. 5B shows for illustrative purposes only an example of a liposome encapsulated molecule of one embodiment. -
FIG. 6 shows a block diagram of an overview of a liposome delivery system of combined Aloe Vera components and cannabis components of one embodiment. -
FIG. 7 shows for illustrative purposes only an example of a liposome attaching to human cell and both opening for transfer of Aloe Vera and CBD into the human cell of one embodiment. -
FIG. 8 shows a block diagram of an overview of examples of liposome cannabis product benefits of one embodiment. -
FIG. 9 shows a block diagram of an overview of continuation of examples of liposome cannabis product benefits of one embodiment. -
FIG. 10 shows a block diagram of an overview of examples of cannabinoid component product benefits of one embodiment. -
FIG. 11 shows a block diagram of an overview of examples of CBD component product benefits of one embodiment. -
FIG. 12 shows a block diagram of an overview of examples of Aloe Vera component product benefits of one embodiment. -
FIG. 13 shows for illustrative purposes only an example of nano sensors suspended in an encapsulation delivery application of one embodiment. -
FIG. 14 shows for illustrative purposes only an example of liposome delivery system cellular transfer into a user's skin of one embodiment. -
FIG. 15 shows for illustrative purposes only an example of a cellular transfer augmented reality application previewing treatment potential results of one embodiment. -
FIG. 16 shows for illustrative purposes only an example of a liposome lipid processing devices for encapsulating compounds and creating application delivery products of one embodiment. - In a following description, reference is made to the accompanying drawings, which form a part hereof, and in which is shown by way of illustration a specific example in which the invention may be practiced. It is to be understood that other embodiments may be utilized and structural changes may be made without departing from the scope of the present invention.
- It should be noted that the descriptions that follow, for example, in terms of a method and devices for cellular transfer of compounds with augmented reality application is described for illustrative purposes and the underlying system can apply to any number and multiple types encapsulated molecules. In one embodiment of the present invention, the method and devices for cellular transfer of compounds with augmented reality application can be configured using a combination of CBD and Aloe Vera. The method and devices for cellular transfer of compounds with augmented reality application can be configured to include only encapsulated CBD molecules and can be configured to include only encapsulated Aloe Vera molecules using the present invention.
-
FIG. 1A shows for illustrative purposes only an example of a method and devices for cellular transfer of compounds with augmented reality application of one embodiment.FIG. 1A shows abilayer liposome 100. Thebilayer liposome 100 is shown in a 2D illustration encapsulatingCBD molecules 110 and AloeVera molecules 120. The spherical liposome shape is formed by thehydrophobic tail 130 andhydrophilic head 140 of its compounds in anaqueous solution 150. Cannabinoid compounds including theCBD molecules 110 and Aloe Veramolecules 120 are suspended in theaqueous solution 150 and encapsulated while the liposome is forming of one embodiment. -
FIG. 1A shows a liposome encapsulation of CBD and Aloe Vera molecules in combination. In other embodiments the liposome encapsulation may be used to encapsulate CBD molecules alone and Aloe Vera molecules alone. Separate liposome encapsulation of the two ingredients provides a method in which the proportioning of the separated CBD and Aloe Vera liposome encapsulations may be used to increase the health benefits of each for a specific purpose for a specific medical condition. - For example a treatment product that is targeted for persons suffering from depression may receive the benefits of CBD constituents that treat depression in a larger proportion than Aloe Vera constituents that treat depression based on studies on the efficacy of the different constituents for the treatment of depression of one embodiment. A device may be used for blending varying proportions of separately encapsulated cannabinoid compound molecules and Aloe Vera molecules for increasing health benefits of each for a specific purpose for a specific medical condition. The device may be coupled to a digital server, a plurality of databases and a computer.
- The plurality of databases have recorded and stored data on varying proportional formulations of cannabinoid compound molecules and Aloe Vera molecules and their benefits for various medical conditions. The computer is used for querying the database for a specific medical condition and the cannabinoid and Aloe Vera constituent benefits. The digital server is used to instruct the blending device to blend with the liposome lipid in an aqueous solution proportional quantities of the various constituents using the varying proportional formulations of cannabinoid compound molecules and Aloe Vera molecules for blending a beneficial product and delivery system for a human to use for treatment of the specific medical condition of one embodiment.
-
FIG. 1B shows for illustrative purposes only an example of a liposome lipid chemical structure of one embodiment.FIG. 1B shows an example of onelipid chemical structure 160. The liposomes may be made of other lipid chemical structures of lipid compounds used for creatinglipid 170 liposomes. The liposomes created from the lipid compounds and methods are characterized by the ability to inhibit biological activity, open readily due to a change in pH, may open readily due to a change in photo intensity and other characteristics that facilitate the delivery of the encapsulated molecules of one embodiment. -
FIG. 2A shows for illustrative purposes only an example of a liposome encapsulated CBD compound of one embodiment.FIG. 2A shows thebilayer liposome 100 in a 2D illustration encapsulatingCBD molecules 110. Thebilayer liposome 100 encapsulatedCBD molecules 110 form a base for a delivery system for products for consumption by humans. CBD provides a variety of benefits. Some of the benefits include treating anorexia, cachexia, gastrointestinal disorders, and nausea, appetite loss, control diabetes, treat Crohn's symptoms, Mood/behavior conditions, depression, Anxiety, control ADD/ADHD, stress, bipolar, OCD, PTSD, treating asthma, fatigue, hypertension, glaucoma, HIV/Aids, muscular dystrophy, providing relief from cancer and cancer treatment symptoms of one embodiment -
FIG. 2B shows for illustrative purposes only an example of a liposome encapsulated Aloe Vera compound of one embodiment.FIG. 2B shows thebilayer liposome 100 in a 2D illustration encapsulatingAloe Vera molecules 120. Thebilayer liposome 100 encapsulatedAloe Vera molecules 120 form a base for a delivery system for products for consumption by humans. - Aloe vera is a rich source of over 200 naturally occurring nutrients which contain water soluble and fat soluble vitamins, minerals, enzymes, polysaccharides, phenolic compounds and organic acids. Its secondary metabolites have multiple properties such as anti-inflammatory, antibacterial, antioxidant, immune boosting, anticancer, antiaging, sunburn relief and antidiabetic potentials. Several traditional uses also have been reported such as burn injury, eczema, cosmetics, inflammation, and fever. Nine categories of phytochemical constituents of Aloe vera can be classified as, anthraquinones, inorganic compounds, amino acids, fatty acids, alkaloids, carbohydrates, enzymes, and vitamins along with other miscellaneous compounds.
- Aloe vera contains 75 potentially active constituents: vitamins, enzymes, minerals, sugars, lignin, saponins, salicylic acids and amino acids. Aloe vera vitamins include vitamins A (beta-carotene), C and E, which are antioxidants and vitamin B12, folic acid, and choline. Aloe vera enzymes include aliiase, alkaline phosphatase, amylase, bradykinase, carboxypeptidase, catalase, cellulase, lipase, and peroxidase. Bradykinase helps to reduce excessive inflammation when applied to the skin topically, while others help in the breakdown of sugars and fats.
- Aloe vera minerals include calcium, chromium, copper, selenium, magnesium, manganese, potassium, sodium and zinc. Aloe vera sugars include monosaccharides (glucose and fructose) and polysaccharides (glucomannans/polymannose). These are derived from the mucilage layer of the plant and are known as mucopolysaccharides. The most prominent monosaccharide is mannose-6-phosphate, and the most common polysaccharides are called glucomannans [beta-(1,4)-acetylated mannan]. Acemannan, a prominent glucomannan has also been found. A glycoprotein with antiallergic properties, called alprogen and novel anti-inflammatory compound, C-glucosyl chromone has been isolated from Aloe vera gel.
- Aloe vera anthraquinones include phenolic compounds traditionally known as laxatives and Aloin and emodin act as analgesics, antibacterials and antivirals. Aloe vera fatty acids include 4 plant steroids; cholesterol, campesterol, β-sisosterol and lupeol. All these have anti-inflammatory action and lupeol also possesses antiseptic and analgesic properties. Aloe vera hormones include auxins and gibberellins that help in wound healing and have anti-inflammatory action. Aloe vera other potentially active constituents include 20 of the 22 human required amino acids and 7 of the 8 essential amino acids. It also contains salicylic acid that possesses anti-inflammatory and antibacterial properties. Lignin, an inert substance, when included in topical preparations, enhances penetrative effect of the other ingredients into the skin. Saponins that are the soapy substances form about 3% of the gel and have cleansing and antiseptic properties.
- One example of the benefits of Aloe Vera is found in the use of Aloe Vera juice mixed with water and honey used as an effective antimalarial cure in Yemen. There are many other reported and studied uses and benefits throughout the world of one embodiment.
- Some studies characterize the Aloe Vera phytochemical constituents of anthraquinones as one of the most important active ingredients of Aloe Vera. The antiplasmodial activity of Aloe Vera may be explained in the light of the presence of anthraquinones and other quinoid compounds which exert good activity against P. falciparum. The four main anthraquinones showing quite high medical values are acemannan, aloe-emodin, aloe bitter and aloe lectin of one embodiment.
-
FIG. 2C shows for illustrative purposes only an example of a liposome encapsulated Inflacin compound of one embodiment.FIG. 2C shows thebilayer liposome 100 in a 2D illustration encapsulatingInflacin molecules 200. Thebilayer liposome 100 encapsulatedInflacin molecules 200 form a base for a delivery system for products for consumption by humans. A group of compounds called Inflacin may be topically applied to alleviate pain associated with arthritis and increased joint mobility. - Inflacin provides its analgesic benefit when applying the topical cream to areas of the body affected by stiffness, soreness and pain. These include: hands, feet, knees and shoulders and muscles of the neck, arms, legs and back. liposome encapsulated Inflacin in for example a topical cream delivers rapid absorption through the skin cells to deliver pain relief and increased mobility for example hand gripping within minutes of one embodiment.
-
FIG. 2D shows for illustrative purposes only an example of liposome encapsulated CBD, Aloe Vera, and Inflacin compounds of one embodiment.FIG. 2D shows thebilayer liposome 100 in a 2D illustration encapsulatingCBD molecules 110,Aloe Vera molecules 120, andInflacin molecules 200. These three compounds may be included in the liposome encapsulation process singularly, or in any combination of two or all three as shown. The liposome encapsulation process may also include other compounds for example other cannabinoids for targeting specific medical benefits for specific conditions and symptoms of one embodiment. -
FIG. 3A shows for illustrative purposes only an example of a chemical structure of Aloe Vera compound emodin of one embodiment.FIG. 3A shows a chemical structure of AloeVera compound emodin 300. Anemodin 302 molecule as shown in the chemical structure of AloeVera compound emodin 300 contains anthraquinones that generate reactive oxygen and thus inactivate malaria parasites.Emodin 302 also provides beneficial properties for immunity and inflammation, antioxidant property, inflammatory bowel disease, supportive care of heart failure/function, hypertension and related disorders, diabetes mellitus, aging-related neurological diseases, atopic dermatitis, hepatic inflammation, autoimmune disorders including rheumatoid arthritis and autoimmune diabetes mellitus, renal inflammatory conditions, and infectious diseases of one embodiment. -
FIG. 3B shows for illustrative purposes only an example of a chemical structure of Aloe Vera compound aleosin of one embodiment.FIG. 3B shows a chemical structure of AloeVera compound aleosin 310. Analeosin 312 molecule as shown in the chemical structure of AloeVera compound aleosin 310 and is an active constituent of the herb Aloe Vera. Aloesin suppresses cell growth and metastasis in ovarian cancer SKOV3 cells through the Inhibition of the MAPK Signaling Pathway, and plays a crucial role in anti-inflammatory activity, ultraviolet protection, and antibacterium. Aloesin accelerates skin wound healing by modulating MAPK/Rho and Smad signaling pathways, has antioxidant properties, provides a significant beneficial effect in lowering blood glucose and improving insulin resistance in humans, and the activity of aloesin increases adiponectin production and improves the insulin sensitivity of one embodiment. -
FIG. 3C shows for illustrative purposes only an example of a chemical structure of Aloe Vera compound acemannan of one embodiment.FIG. 3C shows a chemical structure of AloeVera compound acemannan 320.Acemannan 322 is found in the Aloe Vera plant.Acemannan 322 has various properties and benefits including helps cells to be more resistant to viruses and pathogenic bacteria, improves overall cellular metabolism and functioning, promotes healthy inflammation response, provides critical lubrication of joints, aids in the absorption of water, minerals, and nutrients in the GI tract, reduces pain, improves vascular flow, reduces scarring, increases the body's own production of interferon, interleukins, increase the number of antibody forming T-cells in the spleen, increases the number and activity of killer T-cell and increase monocyte activity, soothes and promotes healing of intestinal disorders such as indigestion, heartburn, hyper-acidity, peptic and duodenal ulcers, colitis, and hemorrhoids, promotes healthy kidney function, speeds wound healing, reduces allergic reactions, stimulates bone marrow activity, anti-aging properties, and supports healthy blood pressure of one embodiment. -
FIG. 4A shows for illustrative purposes only an example of a chemical structure of CBD of one embodiment.FIG. 4A shows a chemical structure ofCBD 400 with a molecular name of cannabidiol (CBD) 410. The illustration shows ahydroxyl group 420 bonded to one of a group of carbon atom cyclic rings that create the bonds for the branch and chain structures of one embodiment. -
FIG. 4B shows for illustrative purposes only an example of a chemical structure of THC of one embodiment.FIG. 4B shows a chemical structure ofTHC 430. This chemical structure ofTHC 430 has a molecular name of tetrahydrocannabinol (THC) 440. The illustration shows the carbon atomcyclic ring 450 structures that create the branch bonds.THC 430 is not a legal compound federally. Its use may only be legal in States and only within that State that has legalized its use. Therefore the embodiments of this invention may exclude the addition ofTHC 430 where it is not legal without changing the method or non-THC embodiments. CBD derived from hemp is federally legal. CBD may also be derived from non-hemp cannabis plants and must meetminimum THC 430 levels to be used for interstate purposes of one embodiment. -
FIG. 5A shows for illustrative purposes only an example of aliposome 3D structure of one embodiment.FIG. 5A shows aliposome 3D structureliposome 3D structureFIG. 5A shows an internalaqueous compartment 510 is created when thehydrophobic tail 130 andhydrophilic head 140 elements of lipid materials are aligned during the cell disruption operation. Theliposome 3D structurehydrophobic tail 130 andhydrophilic head 140 alignments also form bonds between thehydrophilic head 140 elements and the hydrophobic and hydrophilic attractions and repulsions cause the spherical associations of the lipid elements of one embodiment. -
FIG. 5B shows for illustrative purposes only an example of a liposome encapsulated molecule of one embodiment.FIG. 5B shows theliposome 3D structureliposome 3D structuremolecule 520. The suspended molecule fills the internal void during cell disruption and becomes encapsulated as the liposome completes the formation of the bilayer vesicle of one embodiment. -
FIG. 6 shows a block diagram of an overview of a liposome delivery system of combined Aloe Vera components and cannabis components of one embodiment. FIG. 6 shows a liposome delivery system ofAloe Vera components 600emodin 302,aloesin 312 andacemannan 322. A liposome delivery system of combined Aloe Vera components andcannabis components 610 includingemodin 302,aloesin 312,acemannan 322,CBD 400 andTHC 430. A liposome delivery system of cannabinoid andcannabis components 620 withCBD 400 andTHC 430. Other liposome delivery system components including lanolin, retinol, vitamin e, anti-wrinkle creams and treatments for transporting liposome encapsulatedingredients 625. - It should be understood that the selection of both Aloe Vera components and cannabis components can be formulated as any of the components alone or in various combinations of components from each group of Aloe Vera components and cannabis components. The products for oral sublingual ingestion and nasal spray, and suppository insertion and tampon
vaginal insertion 630 or topical applications including underarmtopical application 640 may be formulated for targeting specific medical benefits for specific conditions and symptoms. For example as shown inFIG. 12 Aloe Vera hasanti-inflammatory properties 1237 and cannabis components of a combined group of CBC, CBD, CBDA, CBG, CBN, THC,THCA 925 relieves and reduces arthritis,inflammation 935. - A liposome delivery system may include products for oral sublingual ingestion and nasal spray, and suppository insertion and tampon
vaginal insertion 630 or topical applications including underarmtopical application 640. Liposome delivery system products for oral including sublingual ingestion and nasal spray may include at least one of a group beverages, flavored beverages, pills, capsules, tablets and sprays and for suppository insertion include rectal suppositories used by humans. Liposome delivery system products for topical applications including underarmtopical application 640 include at least one of a group of forms including creams, gels, ointments, salves, sprays, powders, serums, liquids, toners, and oils for use in cosmetics, first aid, and sunscreens by humans. - A liposome delivery system in topical applications including underarm
topical application 640 may be formulated with these combined Aloe Vera and cannabis components to target arthritic inflammation where a topical cream is formed for applying to a person's hands that are suffering from arthritis of one embodiment. - Liposome Attaching to Human Cell and Both Opening for Transfer of Aloe Vera and CBD into the Human Cell:
-
FIG. 7 shows for illustrative purposes only an example of a liposome attaching to human cell and both opening for transfer of Aloe Vera and CBD into the human cell of one embodiment.FIG. 7 shows a liposome encapsulated Aloe Vera andCBD 700 liposome attached to a human cell.FIG. 7 shows a liposome attaching to a human cell and both bilayer structures opening for transfer of Aloe Vera and CBD into thehuman cell 730. A human cell membrane is composed of a lipid bilayer structure. The human cell membrane lipid molecules each have a hydrophilic and a hydrophobic end. Rapid absorption occurs with the liposome bilayer spreading over a human cell. The liposome encapsulatingbilayer structure 710 begins to breach as does thehuman cell 720 membrane upon contact. The liposome bilayer with the encapsulated material reacts with the human cell membrane bilayer wherein the hydrophobic characteristic of the hydrophobic tail grouping creates a breach in the human cell membrane. The encapsulated material passes through the breach into the human cell and the human cell material passes through the breach into newly created voids of the vesicle interior filling the void left by the passing encapsulated material thereby accelerating the rate of the transfer of substances. Once the transfers of the substances are completed the bilayer collapses across the surface of the human cell membrane resealing the human cell membrane and the excess bilayer material is absorbed and excreted through normal bodily functions of one embodiment. -
FIG. 8 shows a block diagram of an overview of examples of liposome cannabis product benefits of one embodiment.FIG. 8 shows examples of liposomecannabis product benefits 800 in different groupings of medical conditions and symptoms. For example conditions related to gastrointestinal 810 involvements. A combination of cannabis product components CBD,THC 820 is used to treat anorexia, cachexia, gastrointestinal disorders, andnausea 830. CBN,THC 822 reducesappetite loss 832. A combination of CBD,THCV 824 helps controldiabetes 834. CBD,THC 826 is used to treat Crohn's 836 symptoms of one embodiment. - Mood/
behavior 840 conditions are treated using a combination of CBC, CBD, CBG, CBN, andTHC 850 fordepression 860. CBD,CBG 852 is used to treatanxiety 862. - CBD,
THC 854 helps control ADD/ADHD,stress 864, attention deficit disorder (ADD) and attention deficit hyperactivity disorder (ADHD). The combination of CBD, CBG, andTHC 856 is used to treat bipolar, OCD,PTSD 866, obsessive-compulsive disorder (OCD) and post-traumatic stress disorder (PTSD) of one embodiment. - Other 870 conditions and symptoms include the use of CBD,
THC 880 for treating asthma, fatigue,hypertension 890, and CBG,THC 881 forglaucoma 891. Another combination of CBD, THC,THCA 882 for treatment of HIV/Aids 892. Treatments with CBC, CBD, CBG, andTHC 883 are beneficial formuscular dystrophy 893. The liposome cannabis product combination of components CBC, CBD, CBDA, CBG, THC, andTHCA 884 is used for providing relief fromcancer 894 and cancer treatment symptoms of one embodiment. The benefits are further described inFIG. 9 . -
FIG. 9 shows a block diagram of an overview of continuation of examples of liposome cannabis product benefits of one embodiment.FIG. 9 shows continuing fromFIG. 8 a continuation of examples of liposome cannabis product benefits 900. Medical conditions that affect pain/sleep 910 can benefit from combinations of cannabis product components for example CBD,THC 920 for treatingsleep apnea 930; CBD,THC 921 for reduced cramps, migraine/headache, phantom limb,spinal injury 931. CBD, CBN,THC 922 is used to treatfibromyalgia 932. CBC, CBD, CBN,THC 923 provides relief forinsomnia 933. The combination of CBC, CBD, CBN, THC, andTHCV 924 reducespain 934. The combined group of CBC, CBD, CBDA, CBG, CBN, THC, andTHCA 925 relieves and reduces arthritis,inflammation 935. -
Neurological 940 conditions are treated using liposome combinations of cannabis product components. CBD,THC 950 is used to treat Tourette's 960 syndrome symptoms. CBD, CBN, THCA,THCV 951 help control epilepsy,seizures 961 onsets. CBCD, CBN, THC,THCA 952 is used to treat the symptoms ofmultiple sclerosis 962. - The combination of CBC, CBD, CBG, THC, and
THCA 953 is used to treat Alzheimer's, Parkinson's 963. CBD, CBG, CBN, THC,THCA 954 reducesspasticity 964. CBC, CBD, CBG, CBN,THCV 955benefit osteoporosis 965 effects. CBC, CBD, CBG, CBN, THC,THCA 956 is used to treatALS 966, Amyotrophic lateral sclerosis (ALS), also known as Lou Gehrig's disease of one embodiment. -
FIG. 10 shows a block diagram of an overview of examples of cannabinoid component product benefits of one embodiment.FIG. 10 shows examples of cannabinoidcomponent product benefits 1000.CBDA 1001 is a cannabinoid component that reducesinflammation 1002 and inhibitscancer cell growth 1003.CBG 1030 is a cannabinoid component that aidssleep 1031, inhibitscancer cell growth 1032, and promotesbone growth 1033. Another cannabinoid component isCBGA 1010 that reducesinflammation 1011, relievespain 1012, and slowsbacterial growth 1013. Yet another cannabinoid component isCBC 1040 with properties that inhibitscancer cell growth 1041, promotesbone growth 1042, reducesinflammation 1043, and relievespain 1044. One of the cannabinoid components isCBCA 1020 that reducesinflammation 1021 and treatsfungal infection 1022. Still another one of the group of cannabinoid components isCBN 1050 that reducesinflammation 1051, relievespain 1052, aidssleep 1053, is anappetite stimulant 1054, and is an anti-convulsive 1055 of one embodiment. -
FIG. 11 shows a block diagram of an overview of examples of CBD component product benefits of one embodiment.FIG. 11 shows examples of CBDcomponent product benefits 1100.CBD 1110 benefits include properties that promotes function in theimmune system 1120, reducessmall intestine contractions 1121, reduces vomiting andnausea 1122, suppressesmuscle spasms 1123, vasorelaxant 1124, tranquillizing 1125, relievespain 1126, relievesanxiety 1127, treatspsoriasis 1128, reducesinflammation 1130, reduces seizures andconvulsions 1131, reduces risk ofartery blockage 1132, reducesblood sugar levels 1133, inhibitscancer cell growth 1134, promotesbone growth 1135, slowsbacterial growth 1136, neuro-protective 1137, and antibacterial 1138 of one embodiment. -
FIG. 12 shows a block diagram of an overview of examples of Aloe Vera component product benefits of one embodiment.FIG. 12 shows examples of Aloe Veracomponent product benefits 1200.Aloe vera 1210 is a succulent has been used for health purposes, dating back to ancient Egypt. TheAloe vera 1210 plant is grown in tropical climates worldwide. It is known for relieving heartburn to potentially slowing the spread of breast cancer, researchers are just beginning to unlock the benefits of this universal plant and its many byproducts. -
Aloe vera 1210 has benefits that include antioxidant andantibacterial properties 1220, lowers the triglyceride levels among people withtype 2diabetes 1221, accelerates the healing ofburns 1222, reducesdental plaque 1223, improve skin and preventwrinkles 1224, lowers blood sugar levels indiabetics 1225, reducehair loss 1226, relievepsoriatic arthritis symptoms 1230, treatacne lesions 1231, keeping skin hydrated and clear 1232, treatskin burns 1233, reduce itchiness andinflammation 1234, a pain reliever salicylic acid found inAloe Vera 1235, treathemorrhoids 1236, andanti-inflammatory properties 1237 of one embodiment. -
FIG. 13 shows for illustrative purposes only an example of nano sensors suspended in an encapsulation delivery application of one embodiment.FIG. 13 shows a plurality ofnano sensors 1300 suspended in delivery application 1310 of a liposome encapsulation ofCBD molecules 110 andAloe Vera molecules 120 in abilayer liposome 100. The plurality ofnano sensors 1300 will be included in a liposome encapsulation of compounds delivery application media 1320 for example a cream for external delivery of the encapsulated compounds for example topical creams. The plurality ofnano sensors 1300 may include temperature sensors, chemical analyzing sensors and other sensors to determine the biological conditions in the cells. The plurality ofnano sensors 1300 may be read using an external device. The external device may include a user digital device with a cellular transfer augmented reality application installed. The external device will receive and process the data gathering results of the plurality ofnano sensors 1300 determinations and prepare a digital and printed report for a user's physician's evaluation for one embodiment. - Liposome Delivery System Cellular Transfer into a User's Skin:
-
FIG. 14 shows for illustrative purposes only an example of liposome delivery system cellular transfer into a user's skin of one embodiment.FIG. 14 shows a user withforehead wrinkles 1400. The user has applied a topical application of the liposome delivery system cellular transfer compounds. An initial liposome opening to transfer compounds intouser cells 1410 takes place open application to the user's skin. A3d depth camera 1420 is used for capturing images of user'sforehead 1425. After the initial period of time wrinkles are beginning to fade 1430. Liposome released compounds are penetrating deeper into the user'sskin 1440. - The
3d depth camera 1420 is capturing images of wrinkles beginning to fade 1455. When the liposome released compounds are fully penetrating deeper into user'sskin 1470 the user's forehead wrinkles are significantly lessened inprominence 1460. The3d depth camera 1420 has been capturing images of the significantly faded wrinkles on the user'sforehead 1485. The user's application of the topical cream of the liposome delivery system cellular transfer compounds has quickly and effectively reduced the user's forehead wrinkles of one embodiment. -
FIG. 15 shows for illustrative purposes only an example of a cellular transfer augmented reality application previewing treatment potential results of one embodiment.FIG. 15 shows acellular transfer network 1500 including adigital server 1510, plurality ofdatabases 1520, a cellular transfer augmentedreality application 1530 installed on a cellulartransfer network computer 1540 and anartificial intelligence 1550 module. A user may connect to thecellular transfer network 1500 via theinternet 1560 using a user's digital device withdepth camera 1570 with the cellular transfer augmentedreality application 1530 installed. In this example the user withforehead wrinkles 1400 can use the depth camera to provide a “before” 3D photograph of the wrinkles. Thecellular transfer network 1500artificial intelligence 1550 module can produce an Augmented Reality (AR) 3D preview for the user to allow the user to see at least an average result using data stored on the plurality ofdatabases 1520. Augmented Reality (AR) is a live, direct or indirect view of a physical, real-world environment whose elements are augmented (or supplemented) by computer-generated sensory input such as sound, video, graphics or GPS data. In this instance the user will see the progress of the wrinkles fading in real time after the application of the topical cream with the liposome delivery system cellular transfer compounds. The user is made aware that their results may differ but based on their physical conditions input this is the possible outcome of one embodiment. -
FIG. 16 shows for illustrative purposes only an example of a liposome lipid processing devices for encapsulating compounds and creating application delivery products of one embodiment.FIG. 16 shows thecellular transfer network 1500,digital server 1510, plurality ofdata bases 1520, cellular transfer augmentedreality application 1530 and cellulartransfer network computer 1540 controlling the production of the lipid liposome encapsulation process and additional processing to create the application delivery products. Theartificial intelligence cloud 1610 monitoring the processing conditions including temperatures, ingredient proportioning to the volume of liposome volume and can adjust those factors to produce a predetermine formulation of the products.cellular transfer network 1500 processes controls 1620 are connected to the processing devices using a processes controlsinterface 1630. For example the temperature of acontainer sterilization processor 1632 is adjusted for the predetermined container type and materials to prevent damaging the container. Aphospholipids supply tank 1640,CBD supply tank 1642 for example and an AloeVera supply tank 1644 for example are shown to convey those compounds into the pre-disruptingliposome combination chamber 1650. Disruptingprocesses 1660 create the conditions for the formation of the liposomes and encapsulation of the compounds in this illustration CBD and Aloe Vera. Depending on the final product being produced for example a production line will include for example a beverage liquid or topicalcream supply tank 1646. A sterilizingmixing tank 1665 is used to blend the liposome encapsulated compounds with the product delivery ingredient. A mixture temperature controller and filling pump withdigital valve 1670 measures the filling of the beverage containers or topicalcream pump containers 1672 and upon completion initiates acontainer capping processor 1674. After capping the containers are processed forpackaging 1680 of one embodiment. - The foregoing has described the principles, embodiments and modes of operation of the present invention. However, the invention should not be construed as being limited to the particular embodiments discussed. The above described embodiments should be regarded as illustrative rather than restrictive, and it should be appreciated that variations may be made in those embodiments by workers skilled in the art without departing from the scope of the present invention as defined by the following claims.
Claims (11)
1. A method, comprising:
suspending legal cannabinoid compound molecules and constituents selected for increasing health benefits of each selected constituent in water;
suspending Aloe Vera molecules and constituents selected for increasing health benefits of each selected constituent in water;
suspending Inflacin molecules in water;
encapsulating within a liposome at least one of a group comprising legal cannabinoid compound molecules and selected constituents, Aloe Vera compound molecules and selected constituents suspended, and Inflacin molecules suspended in water; and
blending at least one of a group comprising liposome encapsulated legal cannabinoid compound molecules and selected constituents, Aloe Vera molecules and selected constituents, and Inflacin molecules into beneficial cellular transfer products and cellular transfer delivery systems for human use.
2. The method of claim 1 , further comprising using a cellular transfer augmented reality application for providing users with a real time simulation of cellular transfer physical results of cellular transfer products.
3. The method of claim 1 , further comprising suspending legal cannabinoid compound molecules including cannabidiol and cannabigerol and selected constituents.
4. The method of claim 1 , further comprising suspending legal cannabinoid compound molecules and its selected constituents in water including Cannabidiol and cannabigerol.
5. The method of claim 1 , further comprising suspending legal cannabinoid compound molecules and selected constituents in water.
6. The method of claim 1 , further comprising suspending Aloe Vera molecules and its selected constituents in water including phytochemical constituents.
7. The method of claim 1 , further comprising suspending Aloe Vera molecules and its selected constituents in water including emodin, aloesin, and acemannan.
8. The method of claim 1 , further comprising encapsulating legal cannabinoid compound molecules and selected constituents and Aloe Vera molecules and selected constituents within a liposome in water may be configured to include varying proportions of separately encapsulated legal cannabinoid compound molecules and selected constituents and Aloe Vera molecules and selected constituents for increasing health benefits of each for a specific purpose for a specific health condition.
9. The method of claim 1 , further comprising blending the liposome encapsulated legal cannabinoid compound molecules and selected constituents and Aloe Vera molecules and selected constituents into a cellular transfer beneficial product and delivery system for oral ingestion including sublingual ingestion by humans.
10. The method of claim 1 , further comprising blending the liposome encapsulated legal cannabinoid compound molecules and selected constituents and Aloe Vera molecules and selected constituents with other ingredients into a healthy beneficial product and delivery system for topical applications by humans.
11-20. (canceled)
Priority Applications (3)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US16/594,039 US20210100746A1 (en) | 2019-10-06 | 2019-10-06 | Method and devices for cellular transfer of compounds with augmented reality application |
US17/962,461 US20230121026A1 (en) | 2019-10-06 | 2022-10-07 | Method and devices for cellular transfer of compounds with augmented reality application |
US18/394,841 US20240260615A1 (en) | 2019-10-06 | 2023-12-22 | Humic and fulvic black water based beverage for human consumption |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US16/594,039 US20210100746A1 (en) | 2019-10-06 | 2019-10-06 | Method and devices for cellular transfer of compounds with augmented reality application |
Related Child Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
US17/962,461 Continuation US20230121026A1 (en) | 2019-10-06 | 2022-10-07 | Method and devices for cellular transfer of compounds with augmented reality application |
Publications (1)
Publication Number | Publication Date |
---|---|
US20210100746A1 true US20210100746A1 (en) | 2021-04-08 |
Family
ID=75273735
Family Applications (3)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
US16/594,039 Abandoned US20210100746A1 (en) | 2019-10-06 | 2019-10-06 | Method and devices for cellular transfer of compounds with augmented reality application |
US17/962,461 Pending US20230121026A1 (en) | 2019-10-06 | 2022-10-07 | Method and devices for cellular transfer of compounds with augmented reality application |
US18/394,841 Pending US20240260615A1 (en) | 2019-10-06 | 2023-12-22 | Humic and fulvic black water based beverage for human consumption |
Family Applications After (2)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
US17/962,461 Pending US20230121026A1 (en) | 2019-10-06 | 2022-10-07 | Method and devices for cellular transfer of compounds with augmented reality application |
US18/394,841 Pending US20240260615A1 (en) | 2019-10-06 | 2023-12-22 | Humic and fulvic black water based beverage for human consumption |
Country Status (1)
Country | Link |
---|---|
US (3) | US20210100746A1 (en) |
Family Cites Families (27)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2380800A (en) * | 1939-05-20 | 1945-07-31 | Howard V Smith | Water treatment |
US5626881A (en) * | 1995-05-16 | 1997-05-06 | Menefee Mining Corporation | Humate dietary supplement |
US6758345B2 (en) * | 2002-02-08 | 2004-07-06 | Aquatune, Inc. | Treatment media for water purification |
KR100549662B1 (en) * | 2003-03-29 | 2006-02-07 | 이뮤노믹스 주식회사 | Composition comprising the extract or fraction isolated from Russian Mumie for activation of Immunity |
CN1287693C (en) * | 2003-07-16 | 2006-12-06 | 刘南凯 | Humic acid healthy drink and application of humic acid to drink |
US7906160B2 (en) * | 2004-10-07 | 2011-03-15 | Next Proteins, Inc. | Protein beverage and method of making the same |
US20080311253A1 (en) * | 2007-06-15 | 2008-12-18 | Sakura Properties, Llc | Gender-specific herbal and mineral supplement drinks |
EP3441323A1 (en) * | 2008-08-29 | 2019-02-13 | Pepsico, Inc. | Post-mix beverage system |
US20120152755A1 (en) * | 2010-12-17 | 2012-06-21 | William John Martin | Energy Charged Liquids to Enhance Enerceutical Activation of the Alternative Cellular Energy (ACE) Pathway in the Therapy of Diseases |
US20120207850A1 (en) * | 2011-02-16 | 2012-08-16 | William John Martin | Methods for Increasing the Kinetic Activity of Alcohol, Water and Other Liquids, so as to Render the Liquids More Useful in Enhancing the Alternative Cellular Energy Pathway in the Prevention and Therapy of Diseases |
US20120213756A1 (en) * | 2011-02-21 | 2012-08-23 | Rosemary Petralia | Nutraceutical beverage |
US20140010922A1 (en) * | 2012-07-09 | 2014-01-09 | William John Martin | Electrostatic Activation of Vaporized Fluids |
US10314874B2 (en) * | 2014-04-08 | 2019-06-11 | Christopher Vandecar | Plant and animal extracts and related methods |
US10000304B2 (en) * | 2014-05-19 | 2018-06-19 | Arthur MONCAYO, JR. | Method for sanitizing and filling containers |
US20150344399A1 (en) * | 2014-06-02 | 2015-12-03 | William John Martin | Heat as a Method to Enhance the Fluid Activating Ability of Humic Acids, Zeolites and related Enerceuticals |
US20180028473A1 (en) * | 2014-06-30 | 2018-02-01 | Mitochondrial Substrate Invention Ltd. | Nutrients solutions |
US20160095877A1 (en) * | 2014-10-06 | 2016-04-07 | William John Martin | Use of Certain Foods and Dietary Supplements as Water and Beverage Activating Enerceuticals |
CN104257843A (en) * | 2014-10-14 | 2015-01-07 | 贵州兴邦生物工程有限公司 | Multi-component compound liquid prepared by minerals and plants as well as preparation method and application of multi-component compound liquid |
WO2017007833A1 (en) * | 2015-07-06 | 2017-01-12 | George Marc | Healthful supplements |
CN106673775A (en) * | 2015-11-05 | 2017-05-17 | 山东泉林纸业有限责任公司 | Humic acid combination and application thereof |
CN106497821A (en) * | 2016-09-20 | 2017-03-15 | 杭州益儒信息科技有限公司 | A kind of food materials are used for the method for probiotic's culture and its application |
CN107260842A (en) * | 2017-07-25 | 2017-10-20 | 冯敏杰 | A kind of anti-large intestine cancer treating oral liquid of compound root of herbaceous peony Sculellaria barbata and its preparation technology |
US10934511B2 (en) * | 2018-09-06 | 2021-03-02 | Louise Wilkie | Humic and fulvic black water based beverage for human consumption |
US10421670B1 (en) * | 2018-07-10 | 2019-09-24 | Louise Wilkie | Humic and fulvic black water based beverage for human consumption |
US10849340B2 (en) * | 2018-07-10 | 2020-12-01 | Louise Wilkie | Humic and fulvic mineral extraction method and beverage for human consumption |
US10918690B2 (en) * | 2018-09-06 | 2021-02-16 | Louise Wilkie | Apparatus and method for processing organic bamboo leaf extract products |
US10894937B2 (en) * | 2019-04-07 | 2021-01-19 | Louise Wilkie | Fulvic acid and humic acid mix for alcoholic beverages method and devices |
-
2019
- 2019-10-06 US US16/594,039 patent/US20210100746A1/en not_active Abandoned
-
2022
- 2022-10-07 US US17/962,461 patent/US20230121026A1/en active Pending
-
2023
- 2023-12-22 US US18/394,841 patent/US20240260615A1/en active Pending
Also Published As
Publication number | Publication date |
---|---|
US20230121026A1 (en) | 2023-04-20 |
US20240260615A1 (en) | 2024-08-08 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
US20090155392A1 (en) | Methods and Systems for Sublingual Guarana Administration | |
Alamgir et al. | Classification of drugs, nutraceuticals, functional food, and cosmeceuticals; proteins, peptides, and enzymes as drugs | |
CN108452275A (en) | It is a kind of to have effects that the composition, medicament and preparation method of relaxing tendons and activating collaterals | |
US20090208593A1 (en) | Phyto aroma micro-nutritherapeutic compositions in orodietology | |
CN101829189B (en) | Traditional Chinese medicine composition for treating allergic dermatitis | |
US20210100746A1 (en) | Method and devices for cellular transfer of compounds with augmented reality application | |
CN116807942A (en) | Centella asiatica extract, guaiacum sky blue hydrocarbon micro-gel beads and preparation method thereof | |
CN101085149A (en) | Porridge containing Chinese yam and almond | |
CN109364011A (en) | It is a kind of to be dissipated and preparation method thereof so that the coated of whitening spot-removing new eight is white | |
Rimple et al. | Poly pharmacological effects of green blood therapy: An update | |
CN109125641A (en) | Compound cortex dictamni ointment and preparation method thereof | |
CN100444850C (en) | Chinese traditional medicine for treating skin diseases | |
CN108785384A (en) | A kind of Chinese medicine composition containing zinc and its preparation for treating acne | |
CN108309910A (en) | Vigor frost and preparation method thereof | |
CN107822135A (en) | A kind of preparation method for the nutrient protected and improve male prostate function | |
CN107753582B (en) | Composition for treating acne, external gel and preparation method thereof | |
CN1294960C (en) | Anti-senescence bee medicine health care preparation | |
CN101669995A (en) | Composite for treatment and health care of heart cerebrovascular diseases and preparation method thereof | |
CA2745579C (en) | Thick pine needle extract composition for capsulation | |
CN106334176B (en) | Chilblain ointment capable of relieving swelling, pain and itching and preparation method thereof | |
CN102772351A (en) | Pearl E cream | |
CN108094776A (en) | A kind of anti-oxidative beverage and its preparation method and application | |
CN107648313A (en) | A kind of Western medicine compound for treating obesity and preparation method thereof | |
CN1785052A (en) | Method for preparing sour milk contg. micron sugared ginseng, bee-glue etc. for tonifying-Yin and nourishing-stomach | |
CN102579642A (en) | Compound grapefruit oil nanoemulsion oral liquid for losing weight and preparation method thereof |
Legal Events
Date | Code | Title | Description |
---|---|---|---|
STPP | Information on status: patent application and granting procedure in general |
Free format text: FINAL REJECTION MAILED |
|
STPP | Information on status: patent application and granting procedure in general |
Free format text: NON FINAL ACTION MAILED |
|
STPP | Information on status: patent application and granting procedure in general |
Free format text: RESPONSE TO NON-FINAL OFFICE ACTION ENTERED AND FORWARDED TO EXAMINER |
|
STPP | Information on status: patent application and granting procedure in general |
Free format text: FINAL REJECTION MAILED |
|
STCB | Information on status: application discontinuation |
Free format text: ABANDONED -- FAILURE TO RESPOND TO AN OFFICE ACTION |