RU2010137392A - Фармацевтические композиции, содержащие глюкагон-подобный пептид 1 (glp-1) - Google Patents
Фармацевтические композиции, содержащие глюкагон-подобный пептид 1 (glp-1) Download PDFInfo
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- RU2010137392A RU2010137392A RU2010137392/15A RU2010137392A RU2010137392A RU 2010137392 A RU2010137392 A RU 2010137392A RU 2010137392/15 A RU2010137392/15 A RU 2010137392/15A RU 2010137392 A RU2010137392 A RU 2010137392A RU 2010137392 A RU2010137392 A RU 2010137392A
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- Prior art keywords
- glp
- diketopiperazine
- powder composition
- dry powder
- composition according
- Prior art date
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- 239000008194 pharmaceutical composition Substances 0.000 title 1
- GCYXWQUSHADNBF-AAEALURTSA-N preproglucagon 78-108 Chemical compound C([C@@H](C(=O)N[C@@H]([C@@H](C)CC)C(=O)N[C@@H](C)C(=O)N[C@@H](CC=1C2=CC=CC=C2NC=1)C(=O)N[C@@H](CC(C)C)C(=O)N[C@@H](C(C)C)C(=O)N[C@@H](CCCCN)C(=O)NCC(=O)N[C@@H](CCCNC(N)=N)C(=O)NCC(O)=O)NC(=O)[C@H](CCC(O)=O)NC(=O)[C@H](CCCCN)NC(=O)[C@H](C)NC(=O)[C@H](C)NC(=O)[C@H](CCC(N)=O)NC(=O)CNC(=O)[C@H](CCC(O)=O)NC(=O)[C@H](CC(C)C)NC(=O)[C@H](CC=1C=CC(O)=CC=1)NC(=O)[C@H](CO)NC(=O)[C@H](CO)NC(=O)[C@@H](NC(=O)[C@H](CC(O)=O)NC(=O)[C@H](CO)NC(=O)[C@@H](NC(=O)[C@H](CC=1C=CC=CC=1)NC(=O)[C@@H](NC(=O)CNC(=O)[C@H](CCC(O)=O)NC(=O)[C@H](C)NC(=O)[C@@H](N)CC=1N=CNC=1)[C@@H](C)O)[C@@H](C)O)C(C)C)C1=CC=CC=C1 GCYXWQUSHADNBF-AAEALURTSA-N 0.000 title 1
- DTHNMHAUYICORS-KTKZVXAJSA-N Glucagon-like peptide 1 Chemical compound C([C@@H](C(=O)N[C@@H]([C@@H](C)CC)C(=O)N[C@@H](C)C(=O)N[C@@H](CC=1C2=CC=CC=C2NC=1)C(=O)N[C@@H](CC(C)C)C(=O)N[C@@H](C(C)C)C(=O)N[C@@H](CCCCN)C(=O)NCC(=O)N[C@@H](CCCNC(N)=N)C(N)=O)NC(=O)[C@H](CCC(O)=O)NC(=O)[C@H](CCCCN)NC(=O)[C@H](C)NC(=O)[C@H](C)NC(=O)[C@H](CCC(N)=O)NC(=O)CNC(=O)[C@H](CCC(O)=O)NC(=O)[C@H](CC(C)C)NC(=O)[C@H](CC=1C=CC(O)=CC=1)NC(=O)[C@H](CO)NC(=O)[C@H](CO)NC(=O)[C@@H](NC(=O)[C@H](CC(O)=O)NC(=O)[C@H](CO)NC(=O)[C@@H](NC(=O)[C@H](CC=1C=CC=CC=1)NC(=O)[C@@H](NC(=O)CNC(=O)[C@H](CCC(O)=O)NC(=O)[C@H](C)NC(=O)[C@@H](N)CC=1N=CNC=1)[C@@H](C)O)[C@@H](C)O)C(C)C)C1=CC=CC=C1 DTHNMHAUYICORS-KTKZVXAJSA-N 0.000 claims abstract 56
- 101710198884 GATA-type zinc finger protein 1 Proteins 0.000 claims abstract 47
- 102100025101 GATA-type zinc finger protein 1 Human genes 0.000 claims abstract 47
- 239000000203 mixture Substances 0.000 claims abstract 18
- 239000000843 powder Substances 0.000 claims abstract 18
- 150000003839 salts Chemical class 0.000 claims abstract 16
- BXRNXXXXHLBUKK-UHFFFAOYSA-N piperazine-2,5-dione Chemical compound O=C1CNC(=O)CN1 BXRNXXXXHLBUKK-UHFFFAOYSA-N 0.000 claims abstract 15
- 238000000034 method Methods 0.000 claims abstract 14
- 239000011859 microparticle Substances 0.000 claims abstract 9
- GLUUGHFHXGJENI-UHFFFAOYSA-N Piperazine Chemical compound C1CNCCN1 GLUUGHFHXGJENI-UHFFFAOYSA-N 0.000 claims abstract 8
- 108090000765 processed proteins & peptides Proteins 0.000 claims abstract 5
- 230000001851 biosynthetic effect Effects 0.000 claims abstract 3
- QGZKDVFQNNGYKY-UHFFFAOYSA-O Ammonium Chemical compound [NH4+] QGZKDVFQNNGYKY-UHFFFAOYSA-O 0.000 claims abstract 2
- OYPRJOBELJOOCE-UHFFFAOYSA-N Calcium Chemical compound [Ca] OYPRJOBELJOOCE-UHFFFAOYSA-N 0.000 claims abstract 2
- 102000003779 Dipeptidyl-peptidases and tripeptidyl-peptidases Human genes 0.000 claims abstract 2
- 108090000194 Dipeptidyl-peptidases and tripeptidyl-peptidases Proteins 0.000 claims abstract 2
- 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 claims abstract 2
- WHXSMMKQMYFTQS-UHFFFAOYSA-N Lithium Chemical compound [Li] WHXSMMKQMYFTQS-UHFFFAOYSA-N 0.000 claims abstract 2
- FYYHWMGAXLPEAU-UHFFFAOYSA-N Magnesium Chemical compound [Mg] FYYHWMGAXLPEAU-UHFFFAOYSA-N 0.000 claims abstract 2
- KZVODIUXIJWGJF-UHFFFAOYSA-N N1CCNCC1.[Na].[Na] Chemical compound N1CCNCC1.[Na].[Na] KZVODIUXIJWGJF-UHFFFAOYSA-N 0.000 claims abstract 2
- ZLMJMSJWJFRBEC-UHFFFAOYSA-N Potassium Chemical compound [K] ZLMJMSJWJFRBEC-UHFFFAOYSA-N 0.000 claims abstract 2
- 239000011575 calcium Substances 0.000 claims abstract 2
- 229910052791 calcium Inorganic materials 0.000 claims abstract 2
- 230000000694 effects Effects 0.000 claims abstract 2
- 108010063245 glucagon-like peptide 1 (7-36)amide Proteins 0.000 claims abstract 2
- -1 glutaryl Chemical group 0.000 claims abstract 2
- 229910052744 lithium Inorganic materials 0.000 claims abstract 2
- 239000011777 magnesium Substances 0.000 claims abstract 2
- 229910052749 magnesium Inorganic materials 0.000 claims abstract 2
- 239000011591 potassium Substances 0.000 claims abstract 2
- 229910052700 potassium Inorganic materials 0.000 claims abstract 2
- 230000002685 pulmonary effect Effects 0.000 claims abstract 2
- 239000011734 sodium Substances 0.000 claims abstract 2
- 229910052708 sodium Inorganic materials 0.000 claims abstract 2
- 125000002730 succinyl group Chemical group C(CCC(=O)*)(=O)* 0.000 claims abstract 2
- 125000005208 trialkylammonium group Chemical group 0.000 claims abstract 2
- 239000002904 solvent Substances 0.000 claims 3
- 238000001694 spray drying Methods 0.000 claims 2
- 208000004476 Acute Coronary Syndrome Diseases 0.000 claims 1
- 208000028698 Cognitive impairment Diseases 0.000 claims 1
- 208000032781 Diabetic cardiomyopathy Diseases 0.000 claims 1
- 102000016622 Dipeptidyl Peptidase 4 Human genes 0.000 claims 1
- 208000032928 Dyslipidaemia Diseases 0.000 claims 1
- 101000930822 Giardia intestinalis Dipeptidyl-peptidase 4 Proteins 0.000 claims 1
- 208000017170 Lipid metabolism disease Diseases 0.000 claims 1
- 208000008589 Obesity Diseases 0.000 claims 1
- 206010063837 Reperfusion injury Diseases 0.000 claims 1
- 208000006011 Stroke Diseases 0.000 claims 1
- 230000001925 catabolic effect Effects 0.000 claims 1
- 208000010877 cognitive disease Diseases 0.000 claims 1
- 206010012601 diabetes mellitus Diseases 0.000 claims 1
- 201000010099 disease Diseases 0.000 claims 1
- 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 claims 1
- 238000004108 freeze drying Methods 0.000 claims 1
- 201000001421 hyperglycemia Diseases 0.000 claims 1
- 238000002513 implantation Methods 0.000 claims 1
- 208000002551 irritable bowel syndrome Diseases 0.000 claims 1
- 208000028867 ischemia Diseases 0.000 claims 1
- 210000004153 islets of langerhan Anatomy 0.000 claims 1
- 206010027175 memory impairment Diseases 0.000 claims 1
- 208000010125 myocardial infarction Diseases 0.000 claims 1
- 208000015122 neurodegenerative disease Diseases 0.000 claims 1
- 235000020824 obesity Nutrition 0.000 claims 1
- 230000001172 regenerating effect Effects 0.000 claims 1
- 238000001356 surgical procedure Methods 0.000 claims 1
- 238000004519 manufacturing process Methods 0.000 abstract 1
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- Dermatology (AREA)
Abstract
1. Сухая порошкообразная композиция для легочного введения, содержащая микрочастицы, включающие гликагонподобный пептид GLP-1 и фармацевтически приемлемую соль дикетопиперазина. ! 2. Сухая порошкообразная композиция по п.1, где указанный GLP-1 выбран из группы, состоящей из нативных GLP-1, метаболитов GLP-1, аналогов GLP-1, производных GLP-1, GLP-1, защищенных от действия дипептидил-пептидазы IV (DPP-IV), GLP-1-миметиков, аналогов пептида GLP-1 или биосинтетических аналогов GLP-1. ! 3. Сухая порошкообразная композиция по п.1, где указанная фармацевтически приемлемая соль дикетопиперазина, имеет формулу 2,5-дикето-3,6-ди(4-Х-аминобутил)пиперазин, где X выбран из группы, состоящей из сукцинила, глутарила, малеила и фумарила. ! 4. Сухая порошкообразная композиция по п.3, где указанным дикетопиперазином является 2,5-дикето-3,6-ди-(4-фумарил- аминобутил)пиперазин. ! 5. Сухая порошкообразная композиция по п.1, где указанная соль является любой фармацевтически приемлемой солью, выбранной из группы, состоящей из натриевых, калиевых, литиевых, магниевых, кальциевых, аммониевых, или моно-, ди- или три-алкиламмониевых солей. ! 6. Сухая порошкообразная композиция по п.1, где указанная соль является моно-, ди-, или смешанной солью. ! 7. Сухая порошкообразная композиция по п.6, где указанным дикетопиперазином является 2,5-дикето-3,6-ди-(4-фумарил- аминобутил)пиперазина динатриевая соль. ! 8. Сухая порошкообразная композиция по п.1, где указанный GLP-1 выбран из нативного GLP-1 или амидированного GLP-1, или GLP-1 (7-36)амида. ! 9. Способ получения микрочастиц, содержащих GLP-1 и фармацевтически приемлемую соль дикетопиперазина, определенных в п.1, где указанный способ включает стадии обеспечен
Claims (19)
1. Сухая порошкообразная композиция для легочного введения, содержащая микрочастицы, включающие гликагонподобный пептид GLP-1 и фармацевтически приемлемую соль дикетопиперазина.
2. Сухая порошкообразная композиция по п.1, где указанный GLP-1 выбран из группы, состоящей из нативных GLP-1, метаболитов GLP-1, аналогов GLP-1, производных GLP-1, GLP-1, защищенных от действия дипептидил-пептидазы IV (DPP-IV), GLP-1-миметиков, аналогов пептида GLP-1 или биосинтетических аналогов GLP-1.
3. Сухая порошкообразная композиция по п.1, где указанная фармацевтически приемлемая соль дикетопиперазина, имеет формулу 2,5-дикето-3,6-ди(4-Х-аминобутил)пиперазин, где X выбран из группы, состоящей из сукцинила, глутарила, малеила и фумарила.
4. Сухая порошкообразная композиция по п.3, где указанным дикетопиперазином является 2,5-дикето-3,6-ди-(4-фумарил- аминобутил)пиперазин.
5. Сухая порошкообразная композиция по п.1, где указанная соль является любой фармацевтически приемлемой солью, выбранной из группы, состоящей из натриевых, калиевых, литиевых, магниевых, кальциевых, аммониевых, или моно-, ди- или три-алкиламмониевых солей.
6. Сухая порошкообразная композиция по п.1, где указанная соль является моно-, ди-, или смешанной солью.
7. Сухая порошкообразная композиция по п.6, где указанным дикетопиперазином является 2,5-дикето-3,6-ди-(4-фумарил- аминобутил)пиперазина динатриевая соль.
8. Сухая порошкообразная композиция по п.1, где указанный GLP-1 выбран из нативного GLP-1 или амидированного GLP-1, или GLP-1 (7-36)амида.
9. Способ получения микрочастиц, содержащих GLP-1 и фармацевтически приемлемую соль дикетопиперазина, определенных в п.1, где указанный способ включает стадии обеспечения GLP-1; обеспечения дикетопиперазина в форме, образующей микрочастицы или его фармацевтически приемлемой соли; и объединения указанного GLP-1 с указанным дикетопиперазином в форме сораствора, в котором образуются микрочастицы, содержащие указанный GLP-1 и указанную соль дикетопиперазина посредством удаления растворителя.
10. Способ по п.9, в котором растворитель из указанного сораствора удаляют путем лиофилизации или сушки распылением.
11. Способ по п.9, где указанный GLP-1 выбран из группы, состоящей из нативного GLP-1, аналога GLP-1, производного GLP-1, GLP-1, защищенного от действия дипептидил-пептидазы IV (DPP-IV), GLP-1-миметика, аналога пептида GLP-1 или биосинтетического аналога GLP-1.
12. Способ по п.9, где указанный GLP-1 обеспечивают в форме раствора, содержащего GLP-1 в концентрации, составляющей 1 мкг/мл - 50 мг/мл или 0,1 мг/мл - 10 мг/мл, или 0,25 мг/мл.
13. Способ по п.9, где указанный GLP-1 в указанных микрочастицах обладает более высокой стабильностью.
14. Способ по п.9, где указанный сораствор содержит GLP-1 в концентрации 1 мкг/мл - 50 мг/мл или 0,1 мг/мл - 10 мг/мл, или 0,25 мг/мл.
15. Способ введения эффективного количества GLP-1 субъекту, нуждающемуся в этом, включающий введение указанному субъекту композиции, определенной в п.1.
16. Способ по п.15, где указанный способ включает лечение состояния или заболевания, выбранного из группы, состоящей из диабета, ишемии, реперфузионного поражения ткани, дислипидемии, диабетической кардиомиопатии, инфаркта миокарда, острого коронарного синдрома, ожирения, катаболических изменений после хирургического вмешательства, гипергликемии, синдрома раздраженного кишечника, инсульта, нейродегенеративных расстройств, нарушений памяти и познавательных способностей, связанных с имплантацией островковых клеток и регенеративной терапией.
17. Способ по п.15, где введение указанных микрочастиц приводит к улучшенным фармакокинетике, времени полужизни и биологической доступности GLP-1 по сравнению с нативным GLP-1.
18. Способ получения порошкообразной композиции, определенной в п.1 с улучшенным фармакокинетическим профилем GLP-1, включающий стадии: обеспечения GLP-1; обеспечения дикетопиперазина, образующего микрочастицы или его фармацевтически приемлемой соли; объединения указанного GLP-1 и указанного дикетопиперазина для образованием сораствора; и удаления растворителя из указанного сораствора путем сушки распылением с образованием порошка, имеющего улучшенный фармакокинетический профиль GLP-1.
19. Способ по п.18, где указанный улучшенный фармакокинетический профиль GLP-1 включает увеличение времени полужизни GLP-1 на 7,5 мин или более; и/или включает улучшенную биологическую доступность GLP-1 по сравнению с нативным GLP-1.
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| DE4242863A1 (de) * | 1992-12-18 | 1994-06-23 | Boehringer Mannheim Gmbh | Stabile lyophilisierte pharmazeutische Zubereitungen von G-CSF |
| WO1999014239A1 (de) * | 1997-09-12 | 1999-03-25 | Wolf Georg Forssmann | Zusammensetzung zur therapie von diabetes mellitus und fettsucht |
| EP1808438B1 (en) * | 1999-06-29 | 2014-10-01 | MannKind Corporation | Purification and stabilization of peptide and proteins in pharmaceutical agents |
| EP1542712A2 (en) * | 2001-06-01 | 2005-06-22 | Eli Lilly And Company | Glp-1 formulations with protracted time action |
| MXPA04008068A (es) * | 2002-02-20 | 2004-11-26 | Lilly Co Eli | Metodo para administrar moleculas de glp-1. |
| WO2003075834A2 (en) * | 2002-03-08 | 2003-09-18 | Eli Lilly And Company | Activated protein c formulations |
| US20040038865A1 (en) * | 2002-08-01 | 2004-02-26 | Mannkind Corporation | Cell transport compositions and uses thereof |
| CA2493478C (en) * | 2002-08-01 | 2014-11-18 | Mannkind Corporation | Cell transport compositions and uses thereof |
| CA2528007C (en) * | 2003-06-02 | 2012-03-27 | Chiron Corporation | Immunogenic compositions based on microparticles comprising adsorbed toxoid and a polysaccharide-containing antigen |
| BR122019022692B1 (pt) * | 2004-08-23 | 2023-01-10 | Mannkind Corporation | Composição terapêutica em pó seco contendo dicetopiperazina, pelo menos um tipo de cátion e um agente biologicamente ativo |
| WO2007033372A2 (en) * | 2005-09-14 | 2007-03-22 | Mannkind Corporation | Method of drug formulation based on increasing the affinity of crystalline microparticle surfaces for active agents |
| DK1986679T3 (da) * | 2006-02-22 | 2017-11-20 | Mannkind Corp | Fremgangsmåde til forbedring af mikropartiklers farmaceutiske egenskaber omfattende diketopiperazin og et aktivt indholdsstof |
| BRPI0709964A2 (pt) * | 2006-04-14 | 2011-08-02 | Mannkind Corp | formulações farmacêuticas contendo peptìdeo glucagon do tipo 1 (glp-1) |
-
2007
- 2007-04-16 BR BRPI0709964-9A patent/BRPI0709964A2/pt not_active IP Right Cessation
- 2007-04-16 KR KR1020147011316A patent/KR101558829B1/ko active Active
- 2007-04-16 RU RU2010137392/15A patent/RU2542500C2/ru not_active IP Right Cessation
- 2007-04-16 JP JP2009505655A patent/JP5415938B2/ja not_active Expired - Fee Related
- 2007-04-16 KR KR1020157008571A patent/KR20150042304A/ko not_active Ceased
- 2007-04-16 CN CN201410514033.8A patent/CN104288756A/zh active Pending
- 2007-04-16 KR KR1020087027774A patent/KR101438839B1/ko active Active
- 2007-04-16 CA CA002646400A patent/CA2646400A1/en active Pending
- 2007-04-16 MX MX2008013216A patent/MX2008013216A/es active IP Right Grant
- 2007-04-16 RU RU2008144965/15A patent/RU2409349C2/ru not_active IP Right Cessation
- 2007-04-16 EP EP20070760728 patent/EP2010155A2/en not_active Withdrawn
- 2007-04-16 CN CNA200780013424XA patent/CN101453988A/zh active Pending
- 2007-04-16 WO PCT/US2007/066728 patent/WO2007121411A2/en not_active Ceased
- 2007-04-16 AU AU2007238000A patent/AU2007238000B2/en not_active Ceased
-
2013
- 2013-09-17 JP JP2013191549A patent/JP5898156B2/ja active Active
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2014
- 2014-12-23 RU RU2014152320A patent/RU2014152320A/ru not_active Application Discontinuation
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2015
- 2015-07-16 HK HK15106772.4A patent/HK1206241A1/xx unknown
- 2015-11-30 JP JP2015233125A patent/JP2016104736A/ja active Pending
Also Published As
| Publication number | Publication date |
|---|---|
| CN104288756A (zh) | 2015-01-21 |
| RU2542500C2 (ru) | 2015-02-20 |
| CA2646400A1 (en) | 2007-10-25 |
| AU2007238000B2 (en) | 2013-01-17 |
| KR101438839B1 (ko) | 2014-10-02 |
| HK1206241A1 (en) | 2016-01-08 |
| JP5415938B2 (ja) | 2014-02-12 |
| RU2409349C2 (ru) | 2011-01-20 |
| WO2007121411A2 (en) | 2007-10-25 |
| JP2016104736A (ja) | 2016-06-09 |
| KR20080111533A (ko) | 2008-12-23 |
| JP2009533476A (ja) | 2009-09-17 |
| JP5898156B2 (ja) | 2016-04-06 |
| CN101453988A (zh) | 2009-06-10 |
| RU2008144965A (ru) | 2010-05-20 |
| KR101558829B1 (ko) | 2015-10-08 |
| JP2014043445A (ja) | 2014-03-13 |
| EP2010155A2 (en) | 2009-01-07 |
| MX2008013216A (es) | 2008-10-27 |
| KR20150042304A (ko) | 2015-04-20 |
| WO2007121411A3 (en) | 2007-12-13 |
| KR20140072138A (ko) | 2014-06-12 |
| BRPI0709964A2 (pt) | 2011-08-02 |
| AU2007238000A1 (en) | 2007-10-25 |
| RU2014152320A (ru) | 2016-07-20 |
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Legal Events
| Date | Code | Title | Description |
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| MM4A | The patent is invalid due to non-payment of fees |
Effective date: 20170417 |