AR105215A1 - Formulación de depósito que contiene ésteres de ácido cítrico - Google Patents
Formulación de depósito que contiene ésteres de ácido cítricoInfo
- Publication number
- AR105215A1 AR105215A1 ARP160101999A ARP160101999A AR105215A1 AR 105215 A1 AR105215 A1 AR 105215A1 AR P160101999 A ARP160101999 A AR P160101999A AR P160101999 A ARP160101999 A AR P160101999A AR 105215 A1 AR105215 A1 AR 105215A1
- Authority
- AR
- Argentina
- Prior art keywords
- trialkyl
- citrate
- acetyl
- reservoir
- formulation according
- Prior art date
Links
- 239000000203 mixture Substances 0.000 title abstract 7
- 238000009472 formulation Methods 0.000 title abstract 6
- KRKNYBCHXYNGOX-UHFFFAOYSA-N citric acid Chemical compound OC(=O)CC(O)(C(O)=O)CC(O)=O KRKNYBCHXYNGOX-UHFFFAOYSA-N 0.000 title 1
- KRKNYBCHXYNGOX-UHFFFAOYSA-K Citrate Chemical compound [O-]C(=O)CC(O)(CC([O-])=O)C([O-])=O KRKNYBCHXYNGOX-UHFFFAOYSA-K 0.000 abstract 6
- WWXUGNUFCNYMFK-UHFFFAOYSA-N Acetyl citrate Chemical compound CC(=O)OC(=O)CC(O)(C(O)=O)CC(O)=O WWXUGNUFCNYMFK-UHFFFAOYSA-N 0.000 abstract 4
- 125000000217 alkyl group Chemical group 0.000 abstract 2
- 125000004432 carbon atom Chemical group C* 0.000 abstract 2
- 239000012530 fluid Substances 0.000 abstract 2
- CGIGDMFJXJATDK-UHFFFAOYSA-N indomethacin Chemical compound CC1=C(CC(O)=O)C2=CC(OC)=CC=C2N1C(=O)C1=CC=C(Cl)C=C1 CGIGDMFJXJATDK-UHFFFAOYSA-N 0.000 abstract 2
- 238000000034 method Methods 0.000 abstract 2
- -1 (6 - {[4- (pyrazol-1-yl) benzyl] (pyridin-3-ylsulfonyl) aminomethyl} pyridin-2-ylamino) isopropyl Chemical group 0.000 abstract 1
- WLRMANUAADYWEA-NWASOUNVSA-N (S)-timolol maleate Chemical compound OC(=O)\C=C/C(O)=O.CC(C)(C)NC[C@H](O)COC1=NSN=C1N1CCOCC1 WLRMANUAADYWEA-NWASOUNVSA-N 0.000 abstract 1
- KLTZDJNSSCMNAO-UHFFFAOYSA-N 2-[[2-[(2-hydroxyacetyl)amino]pyridin-4-yl]methylsulfanyl]-n-[4-(trifluoromethoxy)phenyl]pyridine-3-carboxamide Chemical compound C1=NC(NC(=O)CO)=CC(CSC=2C(=CC=CN=2)C(=O)NC=2C=CC(OC(F)(F)F)=CC=2)=C1 KLTZDJNSSCMNAO-UHFFFAOYSA-N 0.000 abstract 1
- VOVIALXJUBGFJZ-KWVAZRHASA-N Budesonide Chemical compound C1CC2=CC(=O)C=C[C@]2(C)[C@@H]2[C@@H]1[C@@H]1C[C@H]3OC(CCC)O[C@@]3(C(=O)CO)[C@@]1(C)C[C@@H]2O VOVIALXJUBGFJZ-KWVAZRHASA-N 0.000 abstract 1
- PMATZTZNYRCHOR-CGLBZJNRSA-N Cyclosporin A Chemical compound CC[C@@H]1NC(=O)[C@H]([C@H](O)[C@H](C)C\C=C\C)N(C)C(=O)[C@H](C(C)C)N(C)C(=O)[C@H](CC(C)C)N(C)C(=O)[C@H](CC(C)C)N(C)C(=O)[C@@H](C)NC(=O)[C@H](C)NC(=O)[C@H](CC(C)C)N(C)C(=O)[C@H](C(C)C)NC(=O)[C@H](CC(C)C)N(C)C(=O)CN(C)C1=O PMATZTZNYRCHOR-CGLBZJNRSA-N 0.000 abstract 1
- 229930105110 Cyclosporin A Natural products 0.000 abstract 1
- 108010036949 Cyclosporine Proteins 0.000 abstract 1
- GSDSWSVVBLHKDQ-JTQLQIEISA-N Levofloxacin Chemical compound C([C@@H](N1C2=C(C(C(C(O)=O)=C1)=O)C=C1F)C)OC2=C1N1CCN(C)CC1 GSDSWSVVBLHKDQ-JTQLQIEISA-N 0.000 abstract 1
- 229910019142 PO4 Inorganic materials 0.000 abstract 1
- 125000000218 acetic acid group Chemical group C(C)(=O)* 0.000 abstract 1
- XUZMWHLSFXCVMG-UHFFFAOYSA-N baricitinib Chemical compound C1N(S(=O)(=O)CC)CC1(CC#N)N1N=CC(C=2C=3C=CNC=3N=CN=2)=C1 XUZMWHLSFXCVMG-UHFFFAOYSA-N 0.000 abstract 1
- 230000015572 biosynthetic process Effects 0.000 abstract 1
- 229960004436 budesonide Drugs 0.000 abstract 1
- 239000007853 buffer solution Substances 0.000 abstract 1
- 229960003957 dexamethasone Drugs 0.000 abstract 1
- UREBDLICKHMUKA-CXSFZGCWSA-N dexamethasone Chemical compound C1CC2=CC(=O)C=C[C@]2(C)[C@]2(F)[C@@H]1[C@@H]1C[C@@H](C)[C@@](C(=O)CO)(O)[C@@]1(C)C[C@@H]2O UREBDLICKHMUKA-CXSFZGCWSA-N 0.000 abstract 1
- 229960001193 diclofenac sodium Drugs 0.000 abstract 1
- 239000003814 drug Substances 0.000 abstract 1
- 229960001347 fluocinolone acetonide Drugs 0.000 abstract 1
- FEBLZLNTKCEFIT-VSXGLTOVSA-N fluocinolone acetonide Chemical compound C1([C@@H](F)C2)=CC(=O)C=C[C@]1(C)[C@]1(F)[C@@H]2[C@@H]2C[C@H]3OC(C)(C)O[C@@]3(C(=O)CO)[C@@]2(C)C[C@@H]1O FEBLZLNTKCEFIT-VSXGLTOVSA-N 0.000 abstract 1
- 229960000905 indomethacin Drugs 0.000 abstract 1
- JMMWKPVZQRWMSS-UHFFFAOYSA-N isopropanol acetate Natural products CC(C)OC(C)=O JMMWKPVZQRWMSS-UHFFFAOYSA-N 0.000 abstract 1
- 229940011051 isopropyl acetate Drugs 0.000 abstract 1
- GGXICVAJURFBLW-CEYXHVGTSA-N latanoprost Chemical compound CC(C)OC(=O)CCC\C=C/C[C@H]1[C@@H](O)C[C@@H](O)[C@@H]1CC[C@@H](O)CCC1=CC=CC=C1 GGXICVAJURFBLW-CEYXHVGTSA-N 0.000 abstract 1
- 229960001160 latanoprost Drugs 0.000 abstract 1
- 229960003376 levofloxacin Drugs 0.000 abstract 1
- 239000007788 liquid Substances 0.000 abstract 1
- QEFAQIPZVLVERP-UHFFFAOYSA-N nepafenac Chemical group NC(=O)CC1=CC=CC(C(=O)C=2C=CC=CC=2)=C1N QEFAQIPZVLVERP-UHFFFAOYSA-N 0.000 abstract 1
- 229960001002 nepafenac Drugs 0.000 abstract 1
- 229960004114 olopatadine Drugs 0.000 abstract 1
- JBIMVDZLSHOPLA-LSCVHKIXSA-N olopatadine Chemical compound C1OC2=CC=C(CC(O)=O)C=C2C(=C/CCN(C)C)\C2=CC=CC=C21 JBIMVDZLSHOPLA-LSCVHKIXSA-N 0.000 abstract 1
- NBIIXXVUZAFLBC-UHFFFAOYSA-K phosphate Chemical compound [O-]P([O-])([O-])=O NBIIXXVUZAFLBC-UHFFFAOYSA-K 0.000 abstract 1
- 239000010452 phosphate Substances 0.000 abstract 1
- ZAHRKKWIAAJSAO-UHFFFAOYSA-N rapamycin Natural products COCC(O)C(=C/C(C)C(=O)CC(OC(=O)C1CCCCN1C(=O)C(=O)C2(O)OC(CC(OC)C(=CC=CC=CC(C)CC(C)C(=O)C)C)CCC2C)C(C)CC3CCC(O)C(C3)OC)C ZAHRKKWIAAJSAO-UHFFFAOYSA-N 0.000 abstract 1
- QFJCIRLUMZQUOT-HPLJOQBZSA-N sirolimus Chemical compound C1C[C@@H](O)[C@H](OC)C[C@@H]1C[C@@H](C)[C@H]1OC(=O)[C@@H]2CCCCN2C(=O)C(=O)[C@](O)(O2)[C@H](C)CC[C@H]2C[C@H](OC)/C(C)=C/C=C/C=C/[C@@H](C)C[C@@H](C)C(=O)[C@H](OC)[C@H](O)/C(C)=C/[C@@H](C)C(=O)C1 QFJCIRLUMZQUOT-HPLJOQBZSA-N 0.000 abstract 1
- 229960002930 sirolimus Drugs 0.000 abstract 1
- JGMJQSFLQWGYMQ-UHFFFAOYSA-M sodium;2,6-dichloro-n-phenylaniline;acetate Chemical compound [Na+].CC([O-])=O.ClC1=CC=CC(Cl)=C1NC1=CC=CC=C1 JGMJQSFLQWGYMQ-UHFFFAOYSA-M 0.000 abstract 1
- 229960005221 timolol maleate Drugs 0.000 abstract 1
- YNDXUCZADRHECN-JNQJZLCISA-N triamcinolone acetonide Chemical compound C1CC2=CC(=O)C=C[C@]2(C)[C@]2(F)[C@@H]1[C@@H]1C[C@H]3OC(C)(C)O[C@@]3(C(=O)CO)[C@@]1(C)C[C@@H]2O YNDXUCZADRHECN-JNQJZLCISA-N 0.000 abstract 1
- 229960002117 triamcinolone acetonide Drugs 0.000 abstract 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 abstract 1
Classifications
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- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K47/00—Medicinal preparations characterised by the non-active ingredients used, e.g. carriers or inert additives; Targeting or modifying agents chemically bound to the active ingredient
- A61K47/06—Organic compounds, e.g. natural or synthetic hydrocarbons, polyolefins, mineral oil, petrolatum or ozokerite
- A61K47/08—Organic compounds, e.g. natural or synthetic hydrocarbons, polyolefins, mineral oil, petrolatum or ozokerite containing oxygen, e.g. ethers, acetals, ketones, quinones, aldehydes, peroxides
- A61K47/14—Esters of carboxylic acids, e.g. fatty acid monoglycerides, medium-chain triglycerides, parabens or PEG fatty acid esters
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- A61K31/16—Amides, e.g. hydroxamic acids
- A61K31/165—Amides, e.g. hydroxamic acids having aromatic rings, e.g. colchicine, atenolol, progabide
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- A61K31/196—Carboxylic acids, e.g. valproic acid having an amino group the amino group being directly attached to a ring, e.g. anthranilic acid, mefenamic acid, diclofenac, chlorambucil
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- A61K31/403—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with one nitrogen as the only ring hetero atom, e.g. sulpiride, succinimide, tolmetin, buflomedil condensed with carbocyclic rings, e.g. carbazole
- A61K31/404—Indoles, e.g. pindolol
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- A61K31/56—Compounds containing cyclopenta[a]hydrophenanthrene ring systems; Derivatives thereof, e.g. steroids
- A61K31/57—Compounds containing cyclopenta[a]hydrophenanthrene ring systems; Derivatives thereof, e.g. steroids substituted in position 17 beta by a chain of two carbon atoms, e.g. pregnane or progesterone
- A61K31/573—Compounds containing cyclopenta[a]hydrophenanthrene ring systems; Derivatives thereof, e.g. steroids substituted in position 17 beta by a chain of two carbon atoms, e.g. pregnane or progesterone substituted in position 21, e.g. cortisone, dexamethasone, prednisone or aldosterone
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- Medicinal Chemistry (AREA)
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- Ophthalmology & Optometry (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Organic Chemistry (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Proteomics, Peptides & Aminoacids (AREA)
- Oil, Petroleum & Natural Gas (AREA)
- Inorganic Chemistry (AREA)
- Dermatology (AREA)
- Immunology (AREA)
- Gastroenterology & Hepatology (AREA)
- Communicable Diseases (AREA)
- Oncology (AREA)
- Dispersion Chemistry (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Medicinal Preparation (AREA)
- Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
- Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
Abstract
Reivindicación 1: Una formulación de depósito que comprende un citrato de trialquilo y/o acetil citrato de trialquilo, caracterizada porque los grupos alquilo que posee cada uno del citrato de trialquilo y el acetil citrato de trialquilo son iguales o diferentes, y tienen una cantidad de átomos de carbono de entre 3 y 5. Reivindicación 8: La formulación de depósito de acuerdo con la reivindicación 4 caracterizada porque el medicamento es nepafenac, dexametasona, indometacina, diclofenac sódico, levofloxacina, INCB28050, ciclosporina A, maleato de timolol, fluocinolona acetonida, triamcinolona acetonida, budesonida, olopatadina, latanoprost, (6-{[4-(pirazol-1-il)bencil](piridin-3-ilsulfonil)aminometil}piridin-2-ilamino)acetato de isopropilo, 2-[[[2-[(hidroxiacetil)amino]-4-piridinil] metil]tio]-N-[4-(trifluorometoxi)fenil]-3-piridinacarboxamida, o sirolimus. Reivindicación 10: La formulación de depósito de acuerdo con cualquiera de las reivindicaciones 1 a 8, caracterizada porque comprende por lo menos 0,1% (peso en peso) del citrato de trialquilo y/o el citrato de acetil trialquilo. Reivindicación 12: La formulación de depósito de acuerdo con la reivindicación 11, caracterizada porque la formulación de depósito es para la administración intravítrea, administración subconjuntival o administración intracameral. Reivindicación 14: Un método para la formación de un depósito, caracterizado porque comprende seguir el procedimiento de: poner una composición de líquido que contiene un citrato de trialquilo y/o un acetil citrato de trialquilo en contacto con agua, una solución amortiguadora de pH al fosfato, un cuerpo fluido o un cuerpo fluido simulado, donde los grupos alquilo que posee cada uno del citrato de trialquilo y el acetil citrato de trialquilo son iguales o diferentes, y tienen una cantidad de átomos de carbono de entre 3 y 5.
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
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JP2015133040 | 2015-07-01 |
Publications (1)
Publication Number | Publication Date |
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AR105215A1 true AR105215A1 (es) | 2017-09-13 |
Family
ID=57607818
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
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ARP160101999A AR105215A1 (es) | 2015-07-01 | 2016-06-30 | Formulación de depósito que contiene ésteres de ácido cítrico |
Country Status (11)
Country | Link |
---|---|
US (1) | US20180185489A1 (es) |
EP (1) | EP3318280A4 (es) |
JP (1) | JP6872322B2 (es) |
KR (1) | KR20180023945A (es) |
CN (1) | CN107708738B (es) |
AR (1) | AR105215A1 (es) |
CA (1) | CA2991015A1 (es) |
HK (1) | HK1249443A1 (es) |
RU (1) | RU2749952C2 (es) |
TW (1) | TWI755356B (es) |
WO (1) | WO2017002941A1 (es) |
Families Citing this family (8)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US10682340B2 (en) | 2016-06-30 | 2020-06-16 | Durect Corporation | Depot formulations |
EP3478285A4 (en) | 2016-06-30 | 2020-07-22 | Durect Corporation | DEPOSIT FORMULATIONS |
JP2020059652A (ja) * | 2016-12-26 | 2020-04-16 | 参天製薬株式会社 | タフルプロストとクエン酸エステルとを含有するデポ剤 |
EP3639854A4 (en) | 2017-06-16 | 2021-03-03 | The Doshisha | MTOR INHIBITIVE MEDICINAL PRODUCT FOR THE TREATMENT OR PREVENTION OF OPHTHALMIC SYMPTOMS, DISORDERS, OR DISEASES AND USE THEREOF |
WO2018230713A1 (ja) | 2017-06-16 | 2018-12-20 | 学校法人同志社 | カスパーゼ阻害活性を有する化合物、これらの化合物を含む、角膜内皮の症状、障害または疾患を治療または予防するための医薬およびその応用 |
JP7250685B2 (ja) * | 2017-09-29 | 2023-04-03 | 参天製薬株式会社 | ピリジルアミノ酢酸化合物を含有する医薬 |
US20210106569A1 (en) | 2017-12-21 | 2021-04-15 | Santen Pharmaceutical Co., Ltd. | Omidenepag combination |
TWI842692B (zh) | 2017-12-28 | 2024-05-21 | 日商參天製藥股份有限公司 | 含有吡啶基胺乙酸化合物之醫藥製劑 |
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US4738851A (en) * | 1985-09-27 | 1988-04-19 | University Of Iowa Research Foundation, Inc. | Controlled release ophthalmic gel formulation |
WO2002000137A1 (en) * | 2000-06-28 | 2002-01-03 | Shukla Atul J | Biodegradable vehicles and delivery systems of biologically active substances |
US6960346B2 (en) * | 2002-05-09 | 2005-11-01 | University Of Tennessee Research Foundation | Vehicles for delivery of biologically active substances |
US20050281879A1 (en) * | 2003-11-14 | 2005-12-22 | Guohua Chen | Excipients in drug delivery vehicles |
US9993558B2 (en) * | 2004-10-01 | 2018-06-12 | Ramscor, Inc. | Sustained release eye drop formulations |
US20090239891A1 (en) * | 2006-03-01 | 2009-09-24 | Shukla Atul J | Sustained Release Dosage Forms of Analgesic Medications |
BRPI0714683A2 (pt) * | 2006-07-28 | 2013-03-26 | Pfizer Prod Inc | agonistas ep2 |
US8974814B2 (en) * | 2007-11-12 | 2015-03-10 | California Institute Of Technology | Layered drug delivery polymer monofilament fibers |
CA2746491C (en) * | 2008-12-11 | 2018-01-16 | Massachusetts Institute Of Technology | Contact lens drug delivery device |
US8501800B2 (en) * | 2009-03-05 | 2013-08-06 | Insite Vision Incorporated | Controlled-release ophthalmic vehicles |
EP2415763B1 (en) * | 2009-03-30 | 2016-01-27 | Ube Industries, Ltd. | Pharmaceutical composition for treating or preventing glaucoma |
AU2012325370A1 (en) * | 2011-06-10 | 2014-01-30 | Ramscor, Inc. | Conveniently injectable or implantable sustained-release antioxidant formulations for therapies of ocular maladies or cancer |
SI2717914T1 (sl) * | 2011-06-10 | 2020-07-31 | Ramscor Inc. | Formulacije z zadržanim sproščanjem za dostavo proteinov v oko in postopki njihove priprave |
CN102429862B (zh) * | 2011-11-29 | 2013-05-01 | 江苏德达医药科技有限公司 | 一种聚维酮碘眼用缓释滴眼液 |
US9339496B2 (en) * | 2012-07-13 | 2016-05-17 | Santen Pharmaceutical Co., Ltd. | Composition for treating or preventing glaucoma comprising a sulfonamide compound, and a beta-receptor antagonist |
US20140018350A1 (en) * | 2012-07-13 | 2014-01-16 | Asahi Glass Co., Ltd. | Combination of sulfonamide compound and tafluprost |
TWI643619B (zh) * | 2012-07-13 | 2018-12-11 | 日商參天製藥股份有限公司 | 一種用於預防或治療青光眼或高眼壓症、或降低眼壓之醫藥組合物及其用途 |
JP2014019650A (ja) * | 2012-07-13 | 2014-02-03 | Santen Pharmaceut Co Ltd | スルホンアミド化合物とタフルプロストの組み合わせ |
CN105555271A (zh) * | 2013-09-20 | 2016-05-04 | 参天制药株式会社 | 含有聚乙二醇的组合物 |
US9415038B2 (en) * | 2014-01-10 | 2016-08-16 | Santen Pharmaceutical Co., Ltd. | Pharmaceutical formulations comprising a pyridylaminoacetic acid compound |
-
2016
- 2016-06-30 AR ARP160101999A patent/AR105215A1/es unknown
- 2016-06-30 JP JP2016130111A patent/JP6872322B2/ja active Active
- 2016-06-30 TW TW105120894A patent/TWI755356B/zh active
- 2016-06-30 KR KR1020187000199A patent/KR20180023945A/ko not_active Application Discontinuation
- 2016-06-30 US US15/740,219 patent/US20180185489A1/en not_active Abandoned
- 2016-06-30 WO PCT/JP2016/069522 patent/WO2017002941A1/ja active Application Filing
- 2016-06-30 CA CA2991015A patent/CA2991015A1/en active Pending
- 2016-06-30 RU RU2018101473A patent/RU2749952C2/ru active
- 2016-06-30 EP EP16818049.5A patent/EP3318280A4/en active Pending
- 2016-06-30 CN CN201680038495.4A patent/CN107708738B/zh active Active
-
2018
- 2018-07-13 HK HK18109128.6A patent/HK1249443A1/zh unknown
Also Published As
Publication number | Publication date |
---|---|
RU2749952C2 (ru) | 2021-06-21 |
EP3318280A1 (en) | 2018-05-09 |
CN107708738B (zh) | 2022-03-25 |
EP3318280A4 (en) | 2018-08-22 |
KR20180023945A (ko) | 2018-03-07 |
US20180185489A1 (en) | 2018-07-05 |
JP6872322B2 (ja) | 2021-05-19 |
CN107708738A (zh) | 2018-02-16 |
HK1249443A1 (zh) | 2018-11-02 |
RU2018101473A (ru) | 2019-08-01 |
TW201705988A (zh) | 2017-02-16 |
RU2018101473A3 (es) | 2019-11-15 |
TWI755356B (zh) | 2022-02-21 |
CA2991015A1 (en) | 2017-01-05 |
JP2017014209A (ja) | 2017-01-19 |
WO2017002941A1 (ja) | 2017-01-05 |
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