CA2700727A1 - Complex product with advanced assimilation efficacy for humans and its utilization - Google Patents
Complex product with advanced assimilation efficacy for humans and its utilization Download PDFInfo
- Publication number
- CA2700727A1 CA2700727A1 CA2700727A CA2700727A CA2700727A1 CA 2700727 A1 CA2700727 A1 CA 2700727A1 CA 2700727 A CA2700727 A CA 2700727A CA 2700727 A CA2700727 A CA 2700727A CA 2700727 A1 CA2700727 A1 CA 2700727A1
- Authority
- CA
- Canada
- Prior art keywords
- product
- assimilation
- vitamin
- efficacy
- chloride
- 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
- IAZDPXIOMUYVGZ-UHFFFAOYSA-N Dimethylsulphoxide Chemical compound CS(C)=O IAZDPXIOMUYVGZ-UHFFFAOYSA-N 0.000 claims abstract description 20
- ALYNCZNDIQEVRV-UHFFFAOYSA-N 4-aminobenzoic acid Chemical compound NC1=CC=C(C(O)=O)C=C1 ALYNCZNDIQEVRV-UHFFFAOYSA-N 0.000 claims abstract description 14
- 229960001760 dimethyl sulfoxide Drugs 0.000 claims abstract description 10
- 238000004519 manufacturing process Methods 0.000 claims abstract description 9
- ZXYAAVBXHKCJJB-UHFFFAOYSA-N uracil-5-carboxylic acid Chemical compound OC(=O)C1=CNC(=O)NC1=O ZXYAAVBXHKCJJB-UHFFFAOYSA-N 0.000 claims abstract description 9
- 239000004359 castor oil Substances 0.000 claims abstract description 6
- 235000019438 castor oil Nutrition 0.000 claims abstract description 6
- ZEMPKEQAKRGZGQ-XOQCFJPHSA-N glycerol triricinoleate Natural products CCCCCC[C@@H](O)CC=CCCCCCCCC(=O)OC[C@@H](COC(=O)CCCCCCCC=CC[C@@H](O)CCCCCC)OC(=O)CCCCCCCC=CC[C@H](O)CCCCCC ZEMPKEQAKRGZGQ-XOQCFJPHSA-N 0.000 claims abstract description 6
- 235000013305 food Nutrition 0.000 claims description 16
- 238000000034 method Methods 0.000 claims description 9
- MYGVPKMVGSXPCQ-JEDNCBNOSA-N Methylmethionine sulfonium salt Chemical compound [Cl-].C[S+](C)CC[C@H](N)C(O)=O MYGVPKMVGSXPCQ-JEDNCBNOSA-N 0.000 claims description 8
- 210000000936 intestine Anatomy 0.000 claims description 5
- CIWBSHSKHKDKBQ-JLAZNSOCSA-N Ascorbic acid Chemical compound OC[C@H](O)[C@H]1OC(=O)C(O)=C1O CIWBSHSKHKDKBQ-JLAZNSOCSA-N 0.000 claims description 4
- VYGQUTWHTHXGQB-FFHKNEKCSA-N Retinol Palmitate Chemical compound CCCCCCCCCCCCCCCC(=O)OC\C=C(/C)\C=C\C=C(/C)\C=C\C1=C(C)CCCC1(C)C VYGQUTWHTHXGQB-FFHKNEKCSA-N 0.000 claims description 4
- KEAYESYHFKHZAL-UHFFFAOYSA-N Sodium Chemical compound [Na] KEAYESYHFKHZAL-UHFFFAOYSA-N 0.000 claims description 4
- 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 claims description 4
- LXNHXLLTXMVWPM-UHFFFAOYSA-N pyridoxine Chemical compound CC1=NC=C(CO)C(CO)=C1O LXNHXLLTXMVWPM-UHFFFAOYSA-N 0.000 claims description 4
- JIAARYAFYJHUJI-UHFFFAOYSA-L zinc dichloride Chemical compound [Cl-].[Cl-].[Zn+2] JIAARYAFYJHUJI-UHFFFAOYSA-L 0.000 claims description 4
- GHOKWGTUZJEAQD-ZETCQYMHSA-N (D)-(+)-Pantothenic acid Chemical compound OCC(C)(C)[C@@H](O)C(=O)NCCC(O)=O GHOKWGTUZJEAQD-ZETCQYMHSA-N 0.000 claims description 2
- PHIQHXFUZVPYII-ZCFIWIBFSA-N (R)-carnitine Chemical compound C[N+](C)(C)C[C@H](O)CC([O-])=O PHIQHXFUZVPYII-ZCFIWIBFSA-N 0.000 claims description 2
- PZNPLUBHRSSFHT-RRHRGVEJSA-N 1-hexadecanoyl-2-octadecanoyl-sn-glycero-3-phosphocholine Chemical compound CCCCCCCCCCCCCCCCCC(=O)O[C@@H](COP([O-])(=O)OCC[N+](C)(C)C)COC(=O)CCCCCCCCCCCCCCC PZNPLUBHRSSFHT-RRHRGVEJSA-N 0.000 claims description 2
- PWKSKIMOESPYIA-UHFFFAOYSA-N 2-acetamido-3-sulfanylpropanoic acid Chemical compound CC(=O)NC(CS)C(O)=O PWKSKIMOESPYIA-UHFFFAOYSA-N 0.000 claims description 2
- JMGZEFIQIZZSBH-UHFFFAOYSA-N Bioquercetin Natural products CC1OC(OCC(O)C2OC(OC3=C(Oc4cc(O)cc(O)c4C3=O)c5ccc(O)c(O)c5)C(O)C2O)C(O)C(O)C1O JMGZEFIQIZZSBH-UHFFFAOYSA-N 0.000 claims description 2
- VEXZGXHMUGYJMC-UHFFFAOYSA-M Chloride anion Chemical compound [Cl-] VEXZGXHMUGYJMC-UHFFFAOYSA-M 0.000 claims description 2
- AUNGANRZJHBGPY-UHFFFAOYSA-N D-Lyxoflavin Natural products OCC(O)C(O)C(O)CN1C=2C=C(C)C(C)=CC=2N=C2C1=NC(=O)NC2=O AUNGANRZJHBGPY-UHFFFAOYSA-N 0.000 claims description 2
- ZAKOWWREFLAJOT-CEFNRUSXSA-N D-alpha-tocopherylacetate Chemical compound CC(=O)OC1=C(C)C(C)=C2O[C@@](CCC[C@H](C)CCC[C@H](C)CCCC(C)C)(C)CCC2=C1C ZAKOWWREFLAJOT-CEFNRUSXSA-N 0.000 claims description 2
- ZZZCUOFIHGPKAK-UHFFFAOYSA-N D-erythro-ascorbic acid Natural products OCC1OC(=O)C(O)=C1O ZZZCUOFIHGPKAK-UHFFFAOYSA-N 0.000 claims description 2
- WHUUTDBJXJRKMK-UHFFFAOYSA-N Glutamic acid Natural products OC(=O)C(N)CCC(O)=O WHUUTDBJXJRKMK-UHFFFAOYSA-N 0.000 claims description 2
- CKLJMWTZIZZHCS-REOHCLBHSA-N L-aspartic acid Chemical compound OC(=O)[C@@H](N)CC(O)=O CKLJMWTZIZZHCS-REOHCLBHSA-N 0.000 claims description 2
- 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 claims description 2
- DFPAKSUCGFBDDF-UHFFFAOYSA-N Nicotinamide Chemical compound NC(=O)C1=CC=CN=C1 DFPAKSUCGFBDDF-UHFFFAOYSA-N 0.000 claims description 2
- VYGQUTWHTHXGQB-UHFFFAOYSA-N Retinol hexadecanoate Natural products CCCCCCCCCCCCCCCC(=O)OCC=C(C)C=CC=C(C)C=CC1=C(C)CCCC1(C)C VYGQUTWHTHXGQB-UHFFFAOYSA-N 0.000 claims description 2
- AUNGANRZJHBGPY-SCRDCRAPSA-N Riboflavin Chemical compound OC[C@@H](O)[C@@H](O)[C@@H](O)CN1C=2C=C(C)C(C)=CC=2N=C2C1=NC(=O)NC2=O AUNGANRZJHBGPY-SCRDCRAPSA-N 0.000 claims description 2
- 229930003471 Vitamin B2 Natural products 0.000 claims description 2
- 229930003268 Vitamin C Natural products 0.000 claims description 2
- QYSXJUFSXHHAJI-XFEUOLMDSA-N Vitamin D3 Natural products C1(/[C@@H]2CC[C@@H]([C@]2(CCC1)C)[C@H](C)CCCC(C)C)=C/C=C1\C[C@@H](O)CCC1=C QYSXJUFSXHHAJI-XFEUOLMDSA-N 0.000 claims description 2
- MKJXYGKVIBWPFZ-UHFFFAOYSA-L calcium lactate Chemical compound [Ca+2].CC(O)C([O-])=O.CC(O)C([O-])=O MKJXYGKVIBWPFZ-UHFFFAOYSA-L 0.000 claims description 2
- 239000001527 calcium lactate Substances 0.000 claims description 2
- 235000011086 calcium lactate Nutrition 0.000 claims description 2
- 229960002401 calcium lactate Drugs 0.000 claims description 2
- GVPFVAHMJGGAJG-UHFFFAOYSA-L cobalt dichloride Chemical compound [Cl-].[Cl-].[Co+2] GVPFVAHMJGGAJG-UHFFFAOYSA-L 0.000 claims description 2
- ZAKOWWREFLAJOT-UHFFFAOYSA-N d-alpha-Tocopheryl acetate Natural products CC(=O)OC1=C(C)C(C)=C2OC(CCCC(C)CCCC(C)CCCC(C)C)(C)CCC2=C1C ZAKOWWREFLAJOT-UHFFFAOYSA-N 0.000 claims description 2
- IVTMALDHFAHOGL-UHFFFAOYSA-N eriodictyol 7-O-rutinoside Natural products OC1C(O)C(O)C(C)OC1OCC1C(O)C(O)C(O)C(OC=2C=C3C(C(C(O)=C(O3)C=3C=C(O)C(O)=CC=3)=O)=C(O)C=2)O1 IVTMALDHFAHOGL-UHFFFAOYSA-N 0.000 claims description 2
- 229960000304 folic acid Drugs 0.000 claims description 2
- 235000019152 folic acid Nutrition 0.000 claims description 2
- 239000011724 folic acid Substances 0.000 claims description 2
- 235000013922 glutamic acid Nutrition 0.000 claims description 2
- 239000004220 glutamic acid Substances 0.000 claims description 2
- 229960000367 inositol Drugs 0.000 claims description 2
- MEFBJEMVZONFCJ-UHFFFAOYSA-N molybdate Chemical compound [O-][Mo]([O-])(=O)=O MEFBJEMVZONFCJ-UHFFFAOYSA-N 0.000 claims description 2
- 239000006014 omega-3 oil Substances 0.000 claims description 2
- RADKZDMFGJYCBB-UHFFFAOYSA-N pyridoxal hydrochloride Natural products CC1=NC=C(CO)C(C=O)=C1O RADKZDMFGJYCBB-UHFFFAOYSA-N 0.000 claims description 2
- FDRQPMVGJOQVTL-UHFFFAOYSA-N quercetin rutinoside Natural products OC1C(O)C(O)C(CO)OC1OCC1C(O)C(O)C(O)C(OC=2C(C3=C(O)C=C(O)C=C3OC=2C=2C=C(O)C(O)=CC=2)=O)O1 FDRQPMVGJOQVTL-UHFFFAOYSA-N 0.000 claims description 2
- 229940108325 retinyl palmitate Drugs 0.000 claims description 2
- 235000019172 retinyl palmitate Nutrition 0.000 claims description 2
- 239000011769 retinyl palmitate Substances 0.000 claims description 2
- 229960002477 riboflavin Drugs 0.000 claims description 2
- IKGXIBQEEMLURG-BKUODXTLSA-N rutin Chemical compound O[C@H]1[C@H](O)[C@@H](O)[C@H](C)O[C@@H]1OC[C@H]1[C@H](O)[C@@H](O)[C@H](O)[C@@H](OC=2C(C3=C(O)C=C(O)C=C3OC=2C=2C=C(O)C(O)=CC=2)=O)O1 IKGXIBQEEMLURG-BKUODXTLSA-N 0.000 claims description 2
- ALABRVAAKCSLSC-UHFFFAOYSA-N rutin Natural products CC1OC(OCC2OC(O)C(O)C(O)C2O)C(O)C(O)C1OC3=C(Oc4cc(O)cc(O)c4C3=O)c5ccc(O)c(O)c5 ALABRVAAKCSLSC-UHFFFAOYSA-N 0.000 claims description 2
- 235000005493 rutin Nutrition 0.000 claims description 2
- 229960004555 rutoside Drugs 0.000 claims description 2
- 229940082569 selenite Drugs 0.000 claims description 2
- MCAHWIHFGHIESP-UHFFFAOYSA-L selenite(2-) Chemical compound [O-][Se]([O-])=O MCAHWIHFGHIESP-UHFFFAOYSA-L 0.000 claims description 2
- 239000008347 soybean phospholipid Substances 0.000 claims description 2
- FUPJHCRCSQAQET-XRIGFGBMSA-N sulfanium;(2s)-2-(methylamino)-4-methylsulfanylbutanoic acid;iodide Chemical compound [SH3+].[I-].CN[C@H](C(O)=O)CCSC FUPJHCRCSQAQET-XRIGFGBMSA-N 0.000 claims description 2
- 229940042585 tocopherol acetate Drugs 0.000 claims description 2
- 235000019164 vitamin B2 Nutrition 0.000 claims description 2
- 239000011716 vitamin B2 Substances 0.000 claims description 2
- 235000019158 vitamin B6 Nutrition 0.000 claims description 2
- 239000011726 vitamin B6 Substances 0.000 claims description 2
- 235000019154 vitamin C Nutrition 0.000 claims description 2
- 239000011718 vitamin C Substances 0.000 claims description 2
- QYSXJUFSXHHAJI-YRZJJWOYSA-N vitamin D3 Chemical compound C1(/[C@@H]2CC[C@@H]([C@]2(CCC1)C)[C@H](C)CCCC(C)C)=C\C=C1\C[C@@H](O)CCC1=C QYSXJUFSXHHAJI-YRZJJWOYSA-N 0.000 claims description 2
- 235000005282 vitamin D3 Nutrition 0.000 claims description 2
- 239000011647 vitamin D3 Substances 0.000 claims description 2
- 229940011671 vitamin b6 Drugs 0.000 claims description 2
- 229940021056 vitamin d3 Drugs 0.000 claims description 2
- 239000011592 zinc chloride Substances 0.000 claims description 2
- 235000005074 zinc chloride Nutrition 0.000 claims description 2
- 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 claims description 2
- YBJHBAHKTGYVGT-ZKWXMUAHSA-N (+)-Biotin Chemical compound N1C(=O)N[C@@H]2[C@H](CCCCC(=O)O)SC[C@@H]21 YBJHBAHKTGYVGT-ZKWXMUAHSA-N 0.000 claims 1
- QGTJPQKCSDXPDW-XRIGFGBMSA-N (2s)-2-(methylamino)-4-methylsulfanylbutanoic acid;sulfane;hydrochloride Chemical compound [SH3+].[Cl-].CN[C@H](C(O)=O)CCSC QGTJPQKCSDXPDW-XRIGFGBMSA-N 0.000 claims 1
- ODKSFYDXXFIFQN-BYPYZUCNSA-N L-arginine Chemical compound OC(=O)[C@@H](N)CCCN=C(N)N ODKSFYDXXFIFQN-BYPYZUCNSA-N 0.000 claims 1
- 229930064664 L-arginine Natural products 0.000 claims 1
- 235000014852 L-arginine Nutrition 0.000 claims 1
- 229930003451 Vitamin B1 Natural products 0.000 claims 1
- 229940068840 d-biotin Drugs 0.000 claims 1
- -1 methyl-methionine sulphonium iodide carboxyl-uracil Chemical compound 0.000 claims 1
- 229960003495 thiamine Drugs 0.000 claims 1
- DPJRMOMPQZCRJU-UHFFFAOYSA-M thiamine hydrochloride Chemical compound Cl.[Cl-].CC1=C(CCO)SC=[N+]1CC1=CN=C(C)N=C1N DPJRMOMPQZCRJU-UHFFFAOYSA-M 0.000 claims 1
- 235000010374 vitamin B1 Nutrition 0.000 claims 1
- 239000011691 vitamin B1 Substances 0.000 claims 1
- YDBYJHTYSHBBAU-YFKPBYRVSA-N S-methyl-L-methioninate Chemical compound C[S+](C)CC[C@H](N)C([O-])=O YDBYJHTYSHBBAU-YFKPBYRVSA-N 0.000 abstract 1
- RWSOTUBLDIXVET-UHFFFAOYSA-O sulfonium Chemical compound [SH3+] RWSOTUBLDIXVET-UHFFFAOYSA-O 0.000 abstract 1
- 239000000839 emulsion Substances 0.000 description 6
- 230000009931 harmful effect Effects 0.000 description 6
- 239000000203 mixture Substances 0.000 description 6
- XMBWDFGMSWQBCA-UHFFFAOYSA-N hydrogen iodide Chemical compound I XMBWDFGMSWQBCA-UHFFFAOYSA-N 0.000 description 5
- 239000000843 powder Substances 0.000 description 5
- 239000002253 acid Substances 0.000 description 4
- 239000002775 capsule Substances 0.000 description 4
- 230000002354 daily effect Effects 0.000 description 4
- 239000000126 substance Substances 0.000 description 4
- 238000001356 surgical procedure Methods 0.000 description 4
- ZLMJMSJWJFRBEC-UHFFFAOYSA-N Potassium Chemical compound [K] ZLMJMSJWJFRBEC-UHFFFAOYSA-N 0.000 description 3
- 230000032683 aging Effects 0.000 description 3
- 210000004027 cell Anatomy 0.000 description 3
- 210000004207 dermis Anatomy 0.000 description 3
- 229910052500 inorganic mineral Inorganic materials 0.000 description 3
- 239000007788 liquid Substances 0.000 description 3
- 239000011707 mineral Substances 0.000 description 3
- 235000010755 mineral Nutrition 0.000 description 3
- 229940088594 vitamin Drugs 0.000 description 3
- 229930003231 vitamin Natural products 0.000 description 3
- 235000013343 vitamin Nutrition 0.000 description 3
- 239000011782 vitamin Substances 0.000 description 3
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 3
- ZCYVEMRRCGMTRW-UHFFFAOYSA-N 7553-56-2 Chemical compound [I] ZCYVEMRRCGMTRW-UHFFFAOYSA-N 0.000 description 2
- 206010020751 Hypersensitivity Diseases 0.000 description 2
- OFOBLEOULBTSOW-UHFFFAOYSA-N Malonic acid Chemical compound OC(=O)CC(O)=O OFOBLEOULBTSOW-UHFFFAOYSA-N 0.000 description 2
- 230000007815 allergy Effects 0.000 description 2
- 229940024606 amino acid Drugs 0.000 description 2
- 235000001014 amino acid Nutrition 0.000 description 2
- 150000001413 amino acids Chemical class 0.000 description 2
- 239000003963 antioxidant agent Substances 0.000 description 2
- 230000003078 antioxidant effect Effects 0.000 description 2
- 235000006708 antioxidants Nutrition 0.000 description 2
- 230000008901 benefit Effects 0.000 description 2
- 238000002512 chemotherapy Methods 0.000 description 2
- 150000001875 compounds Chemical group 0.000 description 2
- 239000000428 dust Substances 0.000 description 2
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- 239000004615 ingredient Substances 0.000 description 2
- 239000011630 iodine Substances 0.000 description 2
- 229910052740 iodine Inorganic materials 0.000 description 2
- 230000004060 metabolic process Effects 0.000 description 2
- 230000008569 process Effects 0.000 description 2
- 230000002285 radioactive effect Effects 0.000 description 2
- 238000001959 radiotherapy Methods 0.000 description 2
- 238000012827 research and development Methods 0.000 description 2
- 238000011282 treatment Methods 0.000 description 2
- 241000894006 Bacteria Species 0.000 description 1
- 108090000790 Enzymes Proteins 0.000 description 1
- 102000004190 Enzymes Human genes 0.000 description 1
- 206010017533 Fungal infection Diseases 0.000 description 1
- 241000233866 Fungi Species 0.000 description 1
- FYYHWMGAXLPEAU-UHFFFAOYSA-N Magnesium Chemical compound [Mg] FYYHWMGAXLPEAU-UHFFFAOYSA-N 0.000 description 1
- 241001465754 Metazoa Species 0.000 description 1
- 208000031888 Mycoses Diseases 0.000 description 1
- NTNWOCRCBQPEKQ-YFKPBYRVSA-N N(omega)-methyl-L-arginine Chemical compound CN=C(N)NCCC[C@H](N)C(O)=O NTNWOCRCBQPEKQ-YFKPBYRVSA-N 0.000 description 1
- 206010028980 Neoplasm Diseases 0.000 description 1
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 description 1
- 239000005864 Sulphur Substances 0.000 description 1
- 241000700605 Viruses Species 0.000 description 1
- 229930003270 Vitamin B Natural products 0.000 description 1
- 239000003242 anti bacterial agent Substances 0.000 description 1
- 230000000845 anti-microbial effect Effects 0.000 description 1
- 229940088710 antibiotic agent Drugs 0.000 description 1
- 235000019789 appetite Nutrition 0.000 description 1
- 230000036528 appetite Effects 0.000 description 1
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 1
- 229960002685 biotin Drugs 0.000 description 1
- 239000011616 biotin Substances 0.000 description 1
- SXDBWCPKPHAZSM-UHFFFAOYSA-M bromate Inorganic materials [O-]Br(=O)=O SXDBWCPKPHAZSM-UHFFFAOYSA-M 0.000 description 1
- 201000011510 cancer Diseases 0.000 description 1
- 210000000170 cell membrane Anatomy 0.000 description 1
- 210000002421 cell wall Anatomy 0.000 description 1
- OZECDDHOAMNMQI-UHFFFAOYSA-H cerium(3+);trisulfate Chemical compound [Ce+3].[Ce+3].[O-]S([O-])(=O)=O.[O-]S([O-])(=O)=O.[O-]S([O-])(=O)=O OZECDDHOAMNMQI-UHFFFAOYSA-H 0.000 description 1
- 230000008859 change Effects 0.000 description 1
- 239000000084 colloidal system Substances 0.000 description 1
- 230000006866 deterioration Effects 0.000 description 1
- 238000011161 development Methods 0.000 description 1
- 230000018109 developmental process Effects 0.000 description 1
- 235000005911 diet Nutrition 0.000 description 1
- 230000000378 dietary effect Effects 0.000 description 1
- 230000001079 digestive effect Effects 0.000 description 1
- 210000002249 digestive system Anatomy 0.000 description 1
- 238000010790 dilution Methods 0.000 description 1
- 239000012895 dilution Substances 0.000 description 1
- 201000010099 disease Diseases 0.000 description 1
- 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 description 1
- 229940079593 drug Drugs 0.000 description 1
- 239000003814 drug Substances 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 238000005516 engineering process Methods 0.000 description 1
- 230000003203 everyday effect Effects 0.000 description 1
- 235000003642 hunger Nutrition 0.000 description 1
- 238000000338 in vitro Methods 0.000 description 1
- PNDPGZBMCMUPRI-UHFFFAOYSA-N iodine Chemical compound II PNDPGZBMCMUPRI-UHFFFAOYSA-N 0.000 description 1
- 230000000670 limiting effect Effects 0.000 description 1
- 239000011777 magnesium Substances 0.000 description 1
- 229910052749 magnesium Inorganic materials 0.000 description 1
- 239000000463 material Substances 0.000 description 1
- 239000002207 metabolite Substances 0.000 description 1
- 235000016709 nutrition Nutrition 0.000 description 1
- 230000035764 nutrition Effects 0.000 description 1
- 239000001301 oxygen Substances 0.000 description 1
- 229910052760 oxygen Inorganic materials 0.000 description 1
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- 230000003019 stabilising effect Effects 0.000 description 1
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- 239000003053 toxin Substances 0.000 description 1
- 231100000765 toxin Toxicity 0.000 description 1
- 108700012359 toxins Proteins 0.000 description 1
- 150000004670 unsaturated fatty acids Chemical class 0.000 description 1
- 235000021122 unsaturated fatty acids Nutrition 0.000 description 1
- 235000019156 vitamin B Nutrition 0.000 description 1
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Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C381/00—Compounds containing carbon and sulfur and having functional groups not covered by groups C07C301/00 - C07C337/00
- C07C381/12—Sulfonium compounds
-
- A—HUMAN NECESSITIES
- A23—FOODS OR FOODSTUFFS; TREATMENT THEREOF, NOT COVERED BY OTHER CLASSES
- A23L—FOODS, FOODSTUFFS OR NON-ALCOHOLIC BEVERAGES, NOT OTHERWISE PROVIDED FOR; PREPARATION OR TREATMENT THEREOF
- A23L33/00—Modifying nutritive qualities of foods; Dietetic products; Preparation or treatment thereof
- A23L33/10—Modifying nutritive qualities of foods; Dietetic products; Preparation or treatment thereof using additives
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P1/00—Drugs for disorders of the alimentary tract or the digestive system
- A61P1/04—Drugs for disorders of the alimentary tract or the digestive system for ulcers, gastritis or reflux esophagitis, e.g. antacids, inhibitors of acid secretion, mucosal protectants
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P1/00—Drugs for disorders of the alimentary tract or the digestive system
- A61P1/14—Prodigestives, e.g. acids, enzymes, appetite stimulants, antidyspeptics, tonics, antiflatulents
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P39/00—General protective or antinoxious agents
- A61P39/06—Free radical scavengers or antioxidants
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C229/00—Compounds containing amino and carboxyl groups bound to the same carbon skeleton
- C07C229/52—Compounds containing amino and carboxyl groups bound to the same carbon skeleton having amino and carboxyl groups bound to carbon atoms of six-membered aromatic rings of the same carbon skeleton
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Abstract
For the manufacturing of a complex product with advanced assimilation efficacy, including methyl-methionine sul-phonium, carboxyl-uracil, paraaminobenzoic acid, dimethyl-sulfoxide and poliethoxy castor oil, and its utilization.
Description
Complex Product with Advanced Assimilation Efficacy for Humans and its Utilization We created our invention with the aim of restoring the appropriate level of food supply that has become reduced or insufficient due to viral-, bacterial-, fungal infections, harmful environmental emissions causing, amongst others, pollen-, and dust allergies, along with radiation-, and chemotherapy treatments, surgeries, UV-, X-ray and radioactive rays.
Also, the aim of the inventon is to improve the assimilation of food that has become insufficient due to ageing as well as the harmful multiple effects caused during the process of natural ageing.
In order for us to achieve these goals, the objective of our invention is to develop and implement the simplest possible procedure that is feasible with ease.
The product, in accordance with the innovation, consists of water-soluble methyl-methionine sulphonium iodide and paraaminobenzoic acid as well as fat-soluble carboxyl-uracil along with a unique emulsion system belonging to the latter to make it water-soluble without limitation.
To produce this emulsion, the invention uses poliethoxy castor oil (ChremophorR EL, BASF) degraded during the metabolism and dimethyl-sulfoxide, thus making the use of the product of the invention possible for humans.
This product is assimilated in the form of water-soluble substance through the intestines, and contains no digestive and other enzymes.
Considering the achievements of state-of-the-art technologies, no publication questioning the novelty of our procedure has been found in the literature.
Although the complex product with vitamins and minerals manufactured for animals under the Patent number of HU 224 444 contains methyl-methionine sulphonium chloride and kalium iodide, ad 1.: they are only used as components in the food, ad 2.: the advantages of the proper use of these two components are not recognised.
Moreover, the emulsion system of the complex product varies too.
Using our method protected by Patent number P0700175 (applied for by ACHENTY
S.A.: /
UY) we can manufacture a water-soluble product for humans that is capable of restoring the reduced efficacy of food assimilation caused by various reasons.
However, this result is achieved using an emulsion system including all the necessary vitamins, amino acids, minerals and micro elements known to be fundamental, that is completely djerent from our patented procedure presented hereby.
In order for us to achieve our goals, and above all, we need to know the reasons that cause reduced assimilation of food, which eventually can be partially or fully stopped, in terminal phase.
Science undoubtedly has already proved that reduced or insufficient assimilation of food and destroyed assimilation dermises are to blame on the so-called free radicals' that are generated both by metabolites, toxins of viruses, bacteria and fungi, and by harmful environmental emissions causing, amongst others, pollen-, and dust allergies along with radiation-, and chemotherapy treatments, surgeries, UV-, X-ray and radioactive rays.
Similarly, unhealthy nutrition habits or dietary rules, N02-N03 content of food along with medicines, antibiotics causing harm to the wall of intestines and destroying the natural flora of intestines will also multiply the number of free radicals.
For the implementation of the innovation, it undoubtedly was of decisive importance for us to recognise that, first of all, we had to clarify the essence of these 'harmful effects' to be able then to restore the normal functioning of the assimilation dermises of the organism.
The essence of free radicals' was also clarified as being one of all different forms containing one electron-deficit oxygen.
This made it clear for us that, in order for us to achieve the goal of our innovation, we had to develop a product that could get food temporarily into the human organism through - and with the help of- its oxidiser-reductor system, called 'redox'.
First, we had to construct this so-called 'redox' system, day-by-day, using the above mentioned building components in a way that the quantity and proportion of them match the fundamental requirements of a starving organism.
We must emphasize this fact, since now it is not replenishing special foods, but supplying the organism with basic foods using our product, stating at the same time that, using this specific product manufactured during our research and development work, we are capable of restoring the normal level of food assimilation with the highest possible.
speed and efficacy.
During the research and development phase, we found the following composition to be the best at restoring reduced or nearly terminal food assimilation:
A mixture of daily dosage of 30-150 mg of Methyl-methionine sulphonium chloride, 0.20-3.15 mg of kalium-iodide, 11-56 mg ofparaaminobenzoic acid and 6.5-31.0 mg of carboxyl-uracil, transformed in a proper way into water-soluble phase.
Water-solubility was achieved with the highest success by the innovation for this specific occasion through a mixture of 15-43 mg of dimethyl-sulfoxide and 70-350 mg of poliethoxy castor oil.
The direct and indirect anti-oxidant effects ofparaaminobenzoic acid along with methyl-methionine sulphonium chloride are well known and so is the anti-microbial effect of paraaminobenzoic acid.
It is known that the carboxyl-uracil remarkably improves the assimilation of minerals, primarily that of magnesium from intestines.
According to the latest research, but mainly theoratical considerations, this product plays an active role in reparing defficiencies of DNA as well.
Also, the aim of the inventon is to improve the assimilation of food that has become insufficient due to ageing as well as the harmful multiple effects caused during the process of natural ageing.
In order for us to achieve these goals, the objective of our invention is to develop and implement the simplest possible procedure that is feasible with ease.
The product, in accordance with the innovation, consists of water-soluble methyl-methionine sulphonium iodide and paraaminobenzoic acid as well as fat-soluble carboxyl-uracil along with a unique emulsion system belonging to the latter to make it water-soluble without limitation.
To produce this emulsion, the invention uses poliethoxy castor oil (ChremophorR EL, BASF) degraded during the metabolism and dimethyl-sulfoxide, thus making the use of the product of the invention possible for humans.
This product is assimilated in the form of water-soluble substance through the intestines, and contains no digestive and other enzymes.
Considering the achievements of state-of-the-art technologies, no publication questioning the novelty of our procedure has been found in the literature.
Although the complex product with vitamins and minerals manufactured for animals under the Patent number of HU 224 444 contains methyl-methionine sulphonium chloride and kalium iodide, ad 1.: they are only used as components in the food, ad 2.: the advantages of the proper use of these two components are not recognised.
Moreover, the emulsion system of the complex product varies too.
Using our method protected by Patent number P0700175 (applied for by ACHENTY
S.A.: /
UY) we can manufacture a water-soluble product for humans that is capable of restoring the reduced efficacy of food assimilation caused by various reasons.
However, this result is achieved using an emulsion system including all the necessary vitamins, amino acids, minerals and micro elements known to be fundamental, that is completely djerent from our patented procedure presented hereby.
In order for us to achieve our goals, and above all, we need to know the reasons that cause reduced assimilation of food, which eventually can be partially or fully stopped, in terminal phase.
Science undoubtedly has already proved that reduced or insufficient assimilation of food and destroyed assimilation dermises are to blame on the so-called free radicals' that are generated both by metabolites, toxins of viruses, bacteria and fungi, and by harmful environmental emissions causing, amongst others, pollen-, and dust allergies along with radiation-, and chemotherapy treatments, surgeries, UV-, X-ray and radioactive rays.
Similarly, unhealthy nutrition habits or dietary rules, N02-N03 content of food along with medicines, antibiotics causing harm to the wall of intestines and destroying the natural flora of intestines will also multiply the number of free radicals.
For the implementation of the innovation, it undoubtedly was of decisive importance for us to recognise that, first of all, we had to clarify the essence of these 'harmful effects' to be able then to restore the normal functioning of the assimilation dermises of the organism.
The essence of free radicals' was also clarified as being one of all different forms containing one electron-deficit oxygen.
This made it clear for us that, in order for us to achieve the goal of our innovation, we had to develop a product that could get food temporarily into the human organism through - and with the help of- its oxidiser-reductor system, called 'redox'.
First, we had to construct this so-called 'redox' system, day-by-day, using the above mentioned building components in a way that the quantity and proportion of them match the fundamental requirements of a starving organism.
We must emphasize this fact, since now it is not replenishing special foods, but supplying the organism with basic foods using our product, stating at the same time that, using this specific product manufactured during our research and development work, we are capable of restoring the normal level of food assimilation with the highest possible.
speed and efficacy.
During the research and development phase, we found the following composition to be the best at restoring reduced or nearly terminal food assimilation:
A mixture of daily dosage of 30-150 mg of Methyl-methionine sulphonium chloride, 0.20-3.15 mg of kalium-iodide, 11-56 mg ofparaaminobenzoic acid and 6.5-31.0 mg of carboxyl-uracil, transformed in a proper way into water-soluble phase.
Water-solubility was achieved with the highest success by the innovation for this specific occasion through a mixture of 15-43 mg of dimethyl-sulfoxide and 70-350 mg of poliethoxy castor oil.
The direct and indirect anti-oxidant effects ofparaaminobenzoic acid along with methyl-methionine sulphonium chloride are well known and so is the anti-microbial effect of paraaminobenzoic acid.
It is known that the carboxyl-uracil remarkably improves the assimilation of minerals, primarily that of magnesium from intestines.
According to the latest research, but mainly theoratical considerations, this product plays an active role in reparing defficiencies of DNA as well.
The dimethyl-sulfoxide is famous for its successful penetration carrying various organic molecules through the dermis, and since it is generated during intermediate-metabolism, its utilization is obvious.
However, it took us by surprise, as it was unexpected, that it was only the dimethyl-sulfoxide that was able to mix carboxyl-uracil with the emulsion system of our innovation.
Adding iodine to the product manufactured during the implemenation phase seems surprising and question was raised as to how such a strong oxidising substance can be mixed with a system that is basically anti-oxidant.
However, on the other hand, iodine is very important for the organism that considerably improves metabolism, which is especially necessary in our case.
In the course of manufacturing the patented product we have come to a surprising result of unexpected when mixing the non-organic iodine, that is kalium iodide, used for this product, with methyl-methionine sulphonium chloride in a separate procedure, during the manufacturing process.
This unexpected surprising result, the new complex iodide, under certain circumstances - that are determined by the actual 'redox-potential' or electro-motor power of various compounds or compound groups existing in the environment of this new complex - is capable of oxidising and reducing, thus it can restore positive or negative fluctuations in the potential of cell walls / cell membranes, caused by various harmful effects, that eventually result in reduced or fully terminated assimilation offoods.
This phenomenon is similar but not identical to the so-called 'dissipative' systems, known to colloid chemists and physio-chemists, such as the mixture of cerium-sulphate, kalium-bromate, malonic acid and sulphur acid, in which the oxidisation status of the mixture changes in time and space within different time windows.
The discovery of this phenomenon is of paramount importance because any kind of positive or negative of change in the 'redox potential ' of given cell-organelles within the cells of living organisms spells out the beginning of harmful effects including all sorts of diseases and processes of ageing as well.
These changes will also bring about fatal deterioration, and, eventually, a complete loss of efficacy of assimilation through the alimentary canal.
This is what makes it clear how crucial it is that, through the development of our innovative product, we can provide a system that contains anti-oxidants the functioning of which will be secured by a 'redox-molecule' that stabilises the system in a complex formula as detailed above.
This stabilising effect can be detected 'in vitro' as well.
However, it took us by surprise, as it was unexpected, that it was only the dimethyl-sulfoxide that was able to mix carboxyl-uracil with the emulsion system of our innovation.
Adding iodine to the product manufactured during the implemenation phase seems surprising and question was raised as to how such a strong oxidising substance can be mixed with a system that is basically anti-oxidant.
However, on the other hand, iodine is very important for the organism that considerably improves metabolism, which is especially necessary in our case.
In the course of manufacturing the patented product we have come to a surprising result of unexpected when mixing the non-organic iodine, that is kalium iodide, used for this product, with methyl-methionine sulphonium chloride in a separate procedure, during the manufacturing process.
This unexpected surprising result, the new complex iodide, under certain circumstances - that are determined by the actual 'redox-potential' or electro-motor power of various compounds or compound groups existing in the environment of this new complex - is capable of oxidising and reducing, thus it can restore positive or negative fluctuations in the potential of cell walls / cell membranes, caused by various harmful effects, that eventually result in reduced or fully terminated assimilation offoods.
This phenomenon is similar but not identical to the so-called 'dissipative' systems, known to colloid chemists and physio-chemists, such as the mixture of cerium-sulphate, kalium-bromate, malonic acid and sulphur acid, in which the oxidisation status of the mixture changes in time and space within different time windows.
The discovery of this phenomenon is of paramount importance because any kind of positive or negative of change in the 'redox potential ' of given cell-organelles within the cells of living organisms spells out the beginning of harmful effects including all sorts of diseases and processes of ageing as well.
These changes will also bring about fatal deterioration, and, eventually, a complete loss of efficacy of assimilation through the alimentary canal.
This is what makes it clear how crucial it is that, through the development of our innovative product, we can provide a system that contains anti-oxidants the functioning of which will be secured by a 'redox-molecule' that stabilises the system in a complex formula as detailed above.
This stabilising effect can be detected 'in vitro' as well.
The paramount importance of the 'redox-status' in the cells of living organism is justified by the discovery that won Mr. Otto Warburg the Nobel prize for proving the anaerob - that is reduction - processes that can be detected in cells infected with cancer.
In the course of the manufacturing the product we created a molecule, including methyl-Imethionine iodide with paraaminobenzoic acid and carboxyl-uracil, that becomes water-soluble by adding poliethoxy castor oil and dimethyl-sulfoxide, that brings us to a product that is capable of restoring reduced or terminated assimilation of foods, on its own.
The manufacturing process of our innovative product consists of four steps:
= The production process of the emulsion system to make the fat-soluble ingredients water-soluble - mixing the dilution - during which we take 6.5-31 mg of carboxyl-uracil with 15-43 mg of dimethyl-sulfoxide and mix them with 0-350 mg of Chremophor EL (BASF) heated to a temperature of 65 degrees Centigrade.
Following the 7-minute mixing, the material that has cooled out is homogenous and ready for packing.
= The production process of 'redox-complex' using methyl-methionine sulphonium chloride and kalium-iodide, - mixing the powder -, during which 30-105 mg of methyl-methionine sulphonium chloride is slowly and thoroughly mixed with 0.20-3.15mg of kalium-iodide for 15 minutes.
= Mixing the 'redox-complex , that was produced first, with 11-56 mg of paraaminobenzoic acid,- mixing the powder -, = Packaging the liquid and powder separately into capsules, but our innovative product makes it possible to have the complex in water-soluble, single-phase format.
The versatility of our innovative product also makes it possible for us - in certain cases, when, for example, feeding through infusion-tube is temporarily necessary - to add to the water-soluble format the daily dosages of vitamins, crucial amino acids, unsaturated fatty acids, macro-, and micro elements, such as:
110-180 mg of calcium-lactate, 75-110 mg of vitamin C, 60-100 mg of glutamic acid, 30-45 mg L-asparagic acid, 28-35 mg of L-arginine, 2 7-33 mg of L-Ornihtine, 15-30 mg of L-Cysteine, 3.6-21.5 mg of L-Carnitine, 35-50 mg of vitamin B], 38-45 mg of vitamin B2, 28-60 mg'of vitamin B6, 38-80 mg of Niacin amid, 15-40 mg of Ca d-pantothenate, 13-45 mg of m-Inositol, 5-20 mg of Folic acid, 6-18 mg of Rutin, 0.15-0.40 mg ofd-Biotin, 0.15-0.24 mg of Natrium selenite, 0.21-0.65 mg of Natrium molybdate, 21-62 mg of FeII-lactate, 0.03-0.1 mg of Cobalt-chloride, 25.4-42.0 mg of Zinc chloride, 10-30 mg of Mangane chloride, 20-80 mg of Omega3 oil, 11-20 mg of vitamin E acetate, 4-21.2 mg of l3 karotin, 70-210 mg of soy-lecithin, 900-3600 IU of vitamin A palmitate and 150-240 IU of vitamin D3.
Another advantage of our innovation, in this case, is that there is no specific order for mixing / deluting the above mentioned ingredients.
Through the following, but not exclusive, exhibits, we'd like to introduce our innovation, bearing in mind that they have no limiting effect on the scope ofprotection of the Patent:
In the course of the manufacturing the product we created a molecule, including methyl-Imethionine iodide with paraaminobenzoic acid and carboxyl-uracil, that becomes water-soluble by adding poliethoxy castor oil and dimethyl-sulfoxide, that brings us to a product that is capable of restoring reduced or terminated assimilation of foods, on its own.
The manufacturing process of our innovative product consists of four steps:
= The production process of the emulsion system to make the fat-soluble ingredients water-soluble - mixing the dilution - during which we take 6.5-31 mg of carboxyl-uracil with 15-43 mg of dimethyl-sulfoxide and mix them with 0-350 mg of Chremophor EL (BASF) heated to a temperature of 65 degrees Centigrade.
Following the 7-minute mixing, the material that has cooled out is homogenous and ready for packing.
= The production process of 'redox-complex' using methyl-methionine sulphonium chloride and kalium-iodide, - mixing the powder -, during which 30-105 mg of methyl-methionine sulphonium chloride is slowly and thoroughly mixed with 0.20-3.15mg of kalium-iodide for 15 minutes.
= Mixing the 'redox-complex , that was produced first, with 11-56 mg of paraaminobenzoic acid,- mixing the powder -, = Packaging the liquid and powder separately into capsules, but our innovative product makes it possible to have the complex in water-soluble, single-phase format.
The versatility of our innovative product also makes it possible for us - in certain cases, when, for example, feeding through infusion-tube is temporarily necessary - to add to the water-soluble format the daily dosages of vitamins, crucial amino acids, unsaturated fatty acids, macro-, and micro elements, such as:
110-180 mg of calcium-lactate, 75-110 mg of vitamin C, 60-100 mg of glutamic acid, 30-45 mg L-asparagic acid, 28-35 mg of L-arginine, 2 7-33 mg of L-Ornihtine, 15-30 mg of L-Cysteine, 3.6-21.5 mg of L-Carnitine, 35-50 mg of vitamin B], 38-45 mg of vitamin B2, 28-60 mg'of vitamin B6, 38-80 mg of Niacin amid, 15-40 mg of Ca d-pantothenate, 13-45 mg of m-Inositol, 5-20 mg of Folic acid, 6-18 mg of Rutin, 0.15-0.40 mg ofd-Biotin, 0.15-0.24 mg of Natrium selenite, 0.21-0.65 mg of Natrium molybdate, 21-62 mg of FeII-lactate, 0.03-0.1 mg of Cobalt-chloride, 25.4-42.0 mg of Zinc chloride, 10-30 mg of Mangane chloride, 20-80 mg of Omega3 oil, 11-20 mg of vitamin E acetate, 4-21.2 mg of l3 karotin, 70-210 mg of soy-lecithin, 900-3600 IU of vitamin A palmitate and 150-240 IU of vitamin D3.
Another advantage of our innovation, in this case, is that there is no specific order for mixing / deluting the above mentioned ingredients.
Through the following, but not exclusive, exhibits, we'd like to introduce our innovation, bearing in mind that they have no limiting effect on the scope ofprotection of the Patent:
Exhibit 1.
For this purpose, we manufactured 1,000 daily dosages of our innovative product (which daily dosage we found sufficient for a 70 kg Chron patient to restore his digestive system which is partly or fully unable to assimilate food) according to the following method:
We mixed 20 gr of carboxyl-uracil and 18 gr of dimethyl-sulfoxide with 210 gr of ChremophorR EL for 7 minutes and stirred steadily in a mixing bowl.
We mixed 102 gr of methyl-methionine sulphonium chloride and 0.30 gr of kalium iodide by stirring for 15 minutes in a laboratory homogeniser, then homogenised this substance once again with an additional 15 gr ofparaaminobenzoic acid.
- We halved both the liquid and the powder, - We packed one of the half quantities, that is 500 dosages, one-by-one, into capsules for voluntary Chron-patients, - We deluted the other half of the quantities with water and mixed in order for us to assess the reaction of the substance during delution with water, should it be needed, Both the emulsion-system and the powdered fraction of the product we have manufactured, following the delution with water separately or in one, is free from sediment, even in case of very thin delution.
Exhibit 2.
Some of the Chron patients were given dosages of our innovative product in capsules your men and three women; one of the men had had 6 cm of his small intestine removed by surgery.
All patients were prescribed to take one liquid and one powder capsule every day.
After 5 days, all the seven patients reported improved appetite, after 2 weeks all of them have put on weights of 1.5-2.3 kg.
Interestingly, the patient that underwent surgery showed the largest rate of growth in weight.
This exhibit proves that the product, manufactured in accordance with the innovaton, itself is capable of restoring terminated or reduced assimilation of food for humans.
For this purpose, we manufactured 1,000 daily dosages of our innovative product (which daily dosage we found sufficient for a 70 kg Chron patient to restore his digestive system which is partly or fully unable to assimilate food) according to the following method:
We mixed 20 gr of carboxyl-uracil and 18 gr of dimethyl-sulfoxide with 210 gr of ChremophorR EL for 7 minutes and stirred steadily in a mixing bowl.
We mixed 102 gr of methyl-methionine sulphonium chloride and 0.30 gr of kalium iodide by stirring for 15 minutes in a laboratory homogeniser, then homogenised this substance once again with an additional 15 gr ofparaaminobenzoic acid.
- We halved both the liquid and the powder, - We packed one of the half quantities, that is 500 dosages, one-by-one, into capsules for voluntary Chron-patients, - We deluted the other half of the quantities with water and mixed in order for us to assess the reaction of the substance during delution with water, should it be needed, Both the emulsion-system and the powdered fraction of the product we have manufactured, following the delution with water separately or in one, is free from sediment, even in case of very thin delution.
Exhibit 2.
Some of the Chron patients were given dosages of our innovative product in capsules your men and three women; one of the men had had 6 cm of his small intestine removed by surgery.
All patients were prescribed to take one liquid and one powder capsule every day.
After 5 days, all the seven patients reported improved appetite, after 2 weeks all of them have put on weights of 1.5-2.3 kg.
Interestingly, the patient that underwent surgery showed the largest rate of growth in weight.
This exhibit proves that the product, manufactured in accordance with the innovaton, itself is capable of restoring terminated or reduced assimilation of food for humans.
5..
Claims (5)
1., The complex product with advanced efficacy in assimilation for humans according to any of claims, that the product contains methyl-methionine sulphonium iodide carboxyl-uracil, paraaminobenzoic acid, dimethyl-sulfoxide and poliethoxy castor oil.
2., The complex product with advanced efficacy in assimilation for humans according to any of claims, that the methyl-methionine sulphonium iodide is made out of kalium-iodide and methyl-methionin sulphonium chloride, in a separate procedure.
3., The complex product with advanced efficacy in assimilation for humans according to any of claims, that, the product, in accordance with Point 2. of claims, is made out of 30-105 weight unit of methyl-methionine sulphonium chloride, 0.20-3.15 weight unit of kalium-iodide, 11-56 weight unit of paraaminobenzoic acid, 5.5-31 weight unit of carboxyl-uracil, 15-43 weight unit of dimethyl-sulfoxide and 70-350 weight unit of poliethoxy castor oil, or the multiple of these weight units.
4., The complex product with advanced efficacy in assimilation for humans according to any of claims, that, the product in accordance with Point 1., of claims, is used for the manufacturing of the product that restores to normal the reduced or terminated capability of assimilation of foods in intestines.
5., The complex product with advanced efficacy in assimilation for humans according to any of claims, that the product, in accordance with Point 1., of claims, in certain cases, can be mixed with:
110-180 mg of calcium-lactate, 75-110 mg of vitamin C, 60-100 mg of glutamic acid, 30-45 mg L-asparagic acid, 28-35 mg of L-arginine, 27-33 mg of L-Ornitin, 15-30 mg L-Cysteine, 3.6-21.5 mg of L-Carnitine, 35-50 mg of vitamin B1, 38-45 mg of vitamin B2, 28-60 mg of vitamin B6, 38-80 mg of Niacin amid, 15-40 mg of Ca d-pantothenate, 13-45 mg of m-Inositol, 5-20 mg of Folic acid, 6-18 mg of Rutin, 0.15-0 40 mg of d-Biotin, 0.15-0.24 mg of Natrium selenite, 0.21-0 65 mg of Natrium molybdate, 21-62 mg of FeII-lactate, 0. 03-0.1 mg of Cobalt-chloride, 25.4-42.0 mg of Zinc chloride, 10-30 mg of Mangane chloride, 20-80 mg of Omega3 oil, 11-20 mg of vitamin E acetate, 4-21.2 mg of .beta. karotin, 70-210 mg of soy-lecithin, 900-3600 IU of vitamin A palmitate and 150-240 IU of vitamin D3.
110-180 mg of calcium-lactate, 75-110 mg of vitamin C, 60-100 mg of glutamic acid, 30-45 mg L-asparagic acid, 28-35 mg of L-arginine, 27-33 mg of L-Ornitin, 15-30 mg L-Cysteine, 3.6-21.5 mg of L-Carnitine, 35-50 mg of vitamin B1, 38-45 mg of vitamin B2, 28-60 mg of vitamin B6, 38-80 mg of Niacin amid, 15-40 mg of Ca d-pantothenate, 13-45 mg of m-Inositol, 5-20 mg of Folic acid, 6-18 mg of Rutin, 0.15-0 40 mg of d-Biotin, 0.15-0.24 mg of Natrium selenite, 0.21-0 65 mg of Natrium molybdate, 21-62 mg of FeII-lactate, 0. 03-0.1 mg of Cobalt-chloride, 25.4-42.0 mg of Zinc chloride, 10-30 mg of Mangane chloride, 20-80 mg of Omega3 oil, 11-20 mg of vitamin E acetate, 4-21.2 mg of .beta. karotin, 70-210 mg of soy-lecithin, 900-3600 IU of vitamin A palmitate and 150-240 IU of vitamin D3.
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
PCT/HU2007/000088 WO2009040590A1 (en) | 2007-09-26 | 2007-09-26 | Complex product with advanced assimilation efficacy for humans and its utilization |
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CA2700727A1 true CA2700727A1 (en) | 2009-04-02 |
Family
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Application Number | Title | Priority Date | Filing Date |
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CA2700727A Abandoned CA2700727A1 (en) | 2007-09-26 | 2007-09-26 | Complex product with advanced assimilation efficacy for humans and its utilization |
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EP (1) | EP2209390A1 (en) |
JP (1) | JP2010540510A (en) |
CN (1) | CN102098930A (en) |
AP (1) | AP2010005243A0 (en) |
AU (1) | AU2007359463A1 (en) |
BR (1) | BRPI0722045A2 (en) |
CA (1) | CA2700727A1 (en) |
EA (1) | EA201070401A1 (en) |
NO (1) | NO20100595L (en) |
WO (1) | WO2009040590A1 (en) |
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ES2347119B2 (en) * | 2009-04-22 | 2011-04-28 | Universidad De Santiago De Compostela | POLYARGININE NANOCAPSULES. |
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Publication number | Priority date | Publication date | Assignee | Title |
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US6592863B2 (en) * | 2000-08-22 | 2003-07-15 | Nestec S.A. | Nutritional composition |
HU224444B1 (en) * | 2002-11-28 | 2005-09-28 | László Szakács | Liquid, water-dilutable composition for animals with complete vitamin and mineral substance content and process for its production |
-
2007
- 2007-09-26 CA CA2700727A patent/CA2700727A1/en not_active Abandoned
- 2007-09-26 EA EA201070401A patent/EA201070401A1/en unknown
- 2007-09-26 AU AU2007359463A patent/AU2007359463A1/en not_active Abandoned
- 2007-09-26 AP AP2010005243A patent/AP2010005243A0/en unknown
- 2007-09-26 JP JP2010526377A patent/JP2010540510A/en not_active Withdrawn
- 2007-09-26 CN CN2007801016274A patent/CN102098930A/en active Pending
- 2007-09-26 BR BRPI0722045-6A patent/BRPI0722045A2/en not_active Application Discontinuation
- 2007-09-26 EP EP07824980A patent/EP2209390A1/en not_active Withdrawn
- 2007-09-26 WO PCT/HU2007/000088 patent/WO2009040590A1/en active Application Filing
-
2010
- 2010-04-23 NO NO20100595A patent/NO20100595L/en not_active Application Discontinuation
Also Published As
Publication number | Publication date |
---|---|
WO2009040590A1 (en) | 2009-04-02 |
BRPI0722045A2 (en) | 2014-03-25 |
CN102098930A (en) | 2011-06-15 |
EA201070401A1 (en) | 2010-10-29 |
EP2209390A1 (en) | 2010-07-28 |
AU2007359463A1 (en) | 2009-04-02 |
NO20100595L (en) | 2010-06-25 |
AP2010005243A0 (en) | 2010-04-30 |
JP2010540510A (en) | 2010-12-24 |
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