RU2009105696A - N-концевое полисиалилирование - Google Patents
N-концевое полисиалилирование Download PDFInfo
- Publication number
- RU2009105696A RU2009105696A RU2009105696/15A RU2009105696A RU2009105696A RU 2009105696 A RU2009105696 A RU 2009105696A RU 2009105696/15 A RU2009105696/15 A RU 2009105696/15A RU 2009105696 A RU2009105696 A RU 2009105696A RU 2009105696 A RU2009105696 A RU 2009105696A
- Authority
- RU
- Russia
- Prior art keywords
- insulin
- polysaccharide
- protein
- composition according
- group
- Prior art date
Links
Classifications
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- 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
- A61K47/50—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 the non-active ingredient being chemically bound to the active ingredient, e.g. polymer-drug conjugates
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- 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
- A61K47/50—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 the non-active ingredient being chemically bound to the active ingredient, e.g. polymer-drug conjugates
- A61K47/51—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 the non-active ingredient being chemically bound to the active ingredient, e.g. polymer-drug conjugates the non-active ingredient being a modifying agent
- A61K47/56—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 the non-active ingredient being chemically bound to the active ingredient, e.g. polymer-drug conjugates the non-active ingredient being a modifying agent the modifying agent being an organic macromolecular compound, e.g. an oligomeric, polymeric or dendrimeric molecule
- A61K47/61—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 the non-active ingredient being chemically bound to the active ingredient, e.g. polymer-drug conjugates the non-active ingredient being a modifying agent the modifying agent being an organic macromolecular compound, e.g. an oligomeric, polymeric or dendrimeric molecule the organic macromolecular compound being a polysaccharide or a derivative thereof
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K38/00—Medicinal preparations containing peptides
- A61K38/16—Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof
- A61K38/17—Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof from animals; from humans
- A61K38/18—Growth factors; Growth regulators
- A61K38/1816—Erythropoietin [EPO]
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K38/00—Medicinal preparations containing peptides
- A61K38/16—Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof
- A61K38/17—Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof from animals; from humans
- A61K38/19—Cytokines; Lymphokines; Interferons
- A61K38/193—Colony stimulating factors [CSF]
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K38/00—Medicinal preparations containing peptides
- A61K38/16—Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof
- A61K38/17—Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof from animals; from humans
- A61K38/22—Hormones
- A61K38/28—Insulins
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K38/00—Medicinal preparations containing peptides
- A61K38/16—Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof
- A61K38/43—Enzymes; Proenzymes; Derivatives thereof
- A61K38/46—Hydrolases (3)
- A61K38/465—Hydrolases (3) acting on ester bonds (3.1), e.g. lipases, ribonucleases
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- 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
- A61K47/10—Alcohols; Phenols; Salts thereof, e.g. glycerol; Polyethylene glycols [PEG]; Poloxamers; PEG/POE alkyl ethers
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P11/00—Drugs for disorders of the respiratory system
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P13/00—Drugs for disorders of the urinary system
- A61P13/12—Drugs for disorders of the urinary system of the kidneys
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P3/00—Drugs for disorders of the metabolism
- A61P3/04—Anorexiants; Antiobesity agents
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P3/00—Drugs for disorders of the metabolism
- A61P3/08—Drugs for disorders of the metabolism for glucose homeostasis
- A61P3/10—Drugs for disorders of the metabolism for glucose homeostasis for hyperglycaemia, e.g. antidiabetics
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P35/00—Antineoplastic agents
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P37/00—Drugs for immunological or allergic disorders
- A61P37/02—Immunomodulators
- A61P37/06—Immunosuppressants, e.g. drugs for graft rejection
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P43/00—Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P5/00—Drugs for disorders of the endocrine system
- A61P5/06—Drugs for disorders of the endocrine system of the anterior pituitary hormones, e.g. TSH, ACTH, FSH, LH, PRL, GH
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P5/00—Drugs for disorders of the endocrine system
- A61P5/48—Drugs for disorders of the endocrine system of the pancreatic hormones
- A61P5/50—Drugs for disorders of the endocrine system of the pancreatic hormones for increasing or potentiating the activity of insulin
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P7/00—Drugs for disorders of the blood or the extracellular fluid
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P7/00—Drugs for disorders of the blood or the extracellular fluid
- A61P7/06—Antianaemics
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07K—PEPTIDES
- C07K14/00—Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof
- C07K14/435—Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof from animals; from humans
- C07K14/475—Growth factors; Growth regulators
- C07K14/505—Erythropoietin [EPO]
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07K—PEPTIDES
- C07K14/00—Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof
- C07K14/435—Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof from animals; from humans
- C07K14/52—Cytokines; Lymphokines; Interferons
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07K—PEPTIDES
- C07K14/00—Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof
- C07K14/435—Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof from animals; from humans
- C07K14/52—Cytokines; Lymphokines; Interferons
- C07K14/53—Colony-stimulating factor [CSF]
- C07K14/535—Granulocyte CSF; Granulocyte-macrophage CSF
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07K—PEPTIDES
- C07K14/00—Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof
- C07K14/435—Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof from animals; from humans
- C07K14/575—Hormones
-
- C—CHEMISTRY; METALLURGY
- C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
- C12N—MICROORGANISMS OR ENZYMES; COMPOSITIONS THEREOF; PROPAGATING, PRESERVING, OR MAINTAINING MICROORGANISMS; MUTATION OR GENETIC ENGINEERING; CULTURE MEDIA
- C12N9/00—Enzymes; Proenzymes; Compositions thereof; Processes for preparing, activating, inhibiting, separating or purifying enzymes
- C12N9/14—Hydrolases (3)
- C12N9/16—Hydrolases (3) acting on ester bonds (3.1)
- C12N9/22—Ribonucleases RNAses, DNAses
-
- C—CHEMISTRY; METALLURGY
- C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
- C12Y—ENZYMES
- C12Y301/00—Hydrolases acting on ester bonds (3.1)
- C12Y301/21—Endodeoxyribonucleases producing 5'-phosphomonoesters (3.1.21)
- C12Y301/21001—Deoxyribonuclease I (3.1.21.1)
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K38/00—Medicinal preparations containing peptides
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y02—TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
- Y02A—TECHNOLOGIES FOR ADAPTATION TO CLIMATE CHANGE
- Y02A50/00—TECHNOLOGIES FOR ADAPTATION TO CLIMATE CHANGE in human health protection, e.g. against extreme weather
- Y02A50/30—Against vector-borne diseases, e.g. mosquito-borne, fly-borne, tick-borne or waterborne diseases whose impact is exacerbated by climate change
Landscapes
- Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Chemical & Material Sciences (AREA)
- General Health & Medical Sciences (AREA)
- Organic Chemistry (AREA)
- Medicinal Chemistry (AREA)
- Engineering & Computer Science (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Veterinary Medicine (AREA)
- Public Health (AREA)
- Animal Behavior & Ethology (AREA)
- Pharmacology & Pharmacy (AREA)
- Zoology (AREA)
- Gastroenterology & Hepatology (AREA)
- Proteomics, Peptides & Aminoacids (AREA)
- Immunology (AREA)
- General Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Genetics & Genomics (AREA)
- Epidemiology (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Diabetes (AREA)
- Molecular Biology (AREA)
- Biochemistry (AREA)
- Wood Science & Technology (AREA)
- Toxicology (AREA)
- Biophysics (AREA)
- Endocrinology (AREA)
- General Engineering & Computer Science (AREA)
- Hematology (AREA)
- Microbiology (AREA)
- Biotechnology (AREA)
- Biomedical Technology (AREA)
- Obesity (AREA)
- Emergency Medicine (AREA)
- Child & Adolescent Psychology (AREA)
- Pulmonology (AREA)
- Transplantation (AREA)
- Urology & Nephrology (AREA)
- Oil, Petroleum & Natural Gas (AREA)
Abstract
1. Композиция, содержащая популяцию полисахаридных производных белка, где белок представляет собой инсулин или подобный инсулину белок, а полисахарид является полисиаловой кислотой и содержит от 20 до 125 единиц сиаловой кислоты, и где популяция состоит в основном только из производных белка, модифицированых на N-конце В-цепи. ! 2. Композиция согласно п.1, где полисиаловая кислота состоит в основном только из единиц сиаловой кислоты. ! 3. Композиция согласно п.1, где инсулин или подобный инсулину белок модифицирован полисахаридом в редуцирующей концевой единице полисахарида. ! 4. Композиция согласно п.2, где полисахаридные производные имеют общую формулу (I): ! ! где ! HNB происходит из B-NH2, что является N-концом В-цепи инсулина или подобного инсулину белка; ! L обозначает связь, соединяющую группу или содержит полипептид или синтетический олигомер; ! GlyO представляет собой единицу сиаловой кислоты; ! причем соединяющая группа, если она присутствует, имеет общую формулу -Y-C(O)-R1-C(O)-; ! где Y представляет собой NR2 или NR2-NR2; R1 представляет собой бифункциональный органический радикал, выбранный из группы, состоящей из алкандиила, арилена, алкарилена, гетероарилена и алкилгетероарилена, любой из которых может быть замещен и/или прерван карбонильной, сложно-эфирной, сульфидной, простой эфирной, амидной и/или аминной связями; ! и R2 представляет собой Н или C1-6алкил. ! 5. Композиция согласно п.4, где L обозначает связь или группу . ! 6. Композиция согласно п.2, где полисахарид содержит 20-60 единиц сиаловой кислоты, наиболее предпочтительно 40-50 единиц сиаловой кислоты. ! 7. Композиция согласно п.1, где полидисперсность анионного полисахарида ме�
Claims (15)
1. Композиция, содержащая популяцию полисахаридных производных белка, где белок представляет собой инсулин или подобный инсулину белок, а полисахарид является полисиаловой кислотой и содержит от 20 до 125 единиц сиаловой кислоты, и где популяция состоит в основном только из производных белка, модифицированых на N-конце В-цепи.
2. Композиция согласно п.1, где полисиаловая кислота состоит в основном только из единиц сиаловой кислоты.
3. Композиция согласно п.1, где инсулин или подобный инсулину белок модифицирован полисахаридом в редуцирующей концевой единице полисахарида.
4. Композиция согласно п.2, где полисахаридные производные имеют общую формулу (I):
где
HNB происходит из B-NH2, что является N-концом В-цепи инсулина или подобного инсулину белка;
L обозначает связь, соединяющую группу или содержит полипептид или синтетический олигомер;
GlyO представляет собой единицу сиаловой кислоты;
причем соединяющая группа, если она присутствует, имеет общую формулу -Y-C(O)-R1-C(O)-;
где Y представляет собой NR2 или NR2-NR2; R1 представляет собой бифункциональный органический радикал, выбранный из группы, состоящей из алкандиила, арилена, алкарилена, гетероарилена и алкилгетероарилена, любой из которых может быть замещен и/или прерван карбонильной, сложно-эфирной, сульфидной, простой эфирной, амидной и/или аминной связями;
и R2 представляет собой Н или C1-6алкил.
6. Композиция согласно п.2, где полисахарид содержит 20-60 единиц сиаловой кислоты, наиболее предпочтительно 40-50 единиц сиаловой кислоты.
7. Композиция согласно п.1, где полидисперсность анионного полисахарида меньше 1,3, предпочтительно меньше 1,2, наиболее предпочтительно меньше 1,1.
8. Композиция согласно п.1, которая является фармацевтической композицией и содержит один или более из фармацевтически приемлемых наполнителей.
9. Композиция согласно п.1 для применения в терапии.
10. Способ получения полисахаридного производного инсулина или подобного инсулину белка, где анионный полисахарид, представляющий собой полисиаловую кислоту, содержащую 20-125 единиц сиаловой кислоты, химически реагирует в основном только с N-концевым амином В-цепи инсулина или подобного инсулину белка.
11. Способ согласно п.10, где анионный полисахарид имеет реакционноспособную альдегидную группу, которая реагирует с инсулином или с подобным инсулину белком, и реакцию модификации проводят при восстанавливающих условиях.
12. Способ согласно п.11, где реакционноспособная альдегидная группа находится на нередуцирующем конце полисахарида.
13. Способ согласно п.11, где реакционноспособный альдегид находится на редуцирующем конце полисахарида, а нередуцирующий конец был сделан пассивным, так что он не реагирует с инсулином или с подобным инсулину белком.
14. Способ согласно п.10, где анионный полисахарид или промежуточный продукт реакции взаимодействует с концевой аминогруппой инсулина или подобного инсулину белка в первом водном растворе с кислотным рН в диапазоне 4,0-6,0, и полученное полисахаридное производное очищают во втором водном растворе с более высоким рН, чем у первого водного раствора в диапазоне 6,5-8,5.
15. Способ согласно п.10, который осуществляется в присутствии добавки к рецептуре, предпочтительно фосфата натрия.
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
EP06117830 | 2006-07-25 | ||
EP06117830.7 | 2006-07-25 |
Publications (2)
Publication Number | Publication Date |
---|---|
RU2009105696A true RU2009105696A (ru) | 2010-08-27 |
RU2432175C2 RU2432175C2 (ru) | 2011-10-27 |
Family
ID=37397314
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
RU2009105696/15A RU2432175C2 (ru) | 2006-07-25 | 2007-07-25 | N-концевое полисиалилирование |
Country Status (10)
Country | Link |
---|---|
US (22) | US8394921B2 (ru) |
EP (6) | EP2630972B1 (ru) |
JP (14) | JP2009544680A (ru) |
KR (1) | KR101400105B1 (ru) |
CN (2) | CN103169984B (ru) |
AT (1) | ATE467642T1 (ru) |
DE (1) | DE602007006492D1 (ru) |
ES (5) | ES2569066T3 (ru) |
RU (1) | RU2432175C2 (ru) |
WO (4) | WO2008012540A1 (ru) |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
RU2472806C1 (ru) * | 2008-10-20 | 2013-01-20 | Юсв Лимитед | Усовершенствованный способ пегилирования белков |
Families Citing this family (36)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
RU2333223C2 (ru) | 2003-08-12 | 2008-09-10 | Лайпоксен Текнолоджиз Лимитед | Альдегидные производные сиаловой кислоты, способы их получения, конъюгаты альдегидных производных сиаловой кислоты и фармацевтическая композиция на их основе |
ES2294535T3 (es) * | 2003-08-12 | 2008-04-01 | Lipoxen Technologies Limited | Derivados del acido polisialico. |
ES2569066T3 (es) | 2006-07-25 | 2016-05-06 | Lipoxen Technologies Limited | Conjugación N-terminal de ácido polisiálico a proteínas |
ES2521490T3 (es) | 2006-12-15 | 2014-11-12 | Baxter International Inc. | Conjugado de factor VIIa - ácido (poli)siálico con una vida media in vivo prolongada. |
DK2115010T3 (da) | 2007-02-28 | 2012-02-06 | Lipoxen Technologies Ltd | Mindskelse af endotoksin i polysialinsyrer |
WO2009024977A2 (en) * | 2007-08-20 | 2009-02-26 | Protalix Ltd. | Saccharide-containing protein conjugates and uses thereof |
EP2344527A4 (en) * | 2008-10-31 | 2012-04-04 | Amgen Inc | MATERIALS AND METHODS FOR STEM CELL MOBILIZATION THROUGH A MULTIPLE PEGYLATED GRANULOCYTE COLONY STIMULATING FACTOR |
US8846103B2 (en) | 2009-01-28 | 2014-09-30 | Smartcells, Inc. | Exogenously triggered controlled release materials and uses thereof |
CA2750269A1 (en) | 2009-01-28 | 2010-08-05 | Smartcells, Inc. | Crystalline insulin-conjugates |
WO2010088294A1 (en) | 2009-01-28 | 2010-08-05 | Smartcells, Inc. | Conjugate based systems for controlled drug delivery |
CA2750252A1 (en) | 2009-01-28 | 2010-08-05 | Smartcells, Inc. | Synthetic conjugates and uses thereof |
AU2010226243A1 (en) | 2009-03-20 | 2011-09-22 | Smartcells, Inc. | Terminally-functionalized conjugates and uses thereof |
US8569231B2 (en) | 2009-03-20 | 2013-10-29 | Smartcells, Inc. | Soluble non-depot insulin conjugates and uses thereof |
US8809501B2 (en) | 2009-07-27 | 2014-08-19 | Baxter International Inc. | Nucleophilic catalysts for oxime linkage |
ES2590679T3 (es) * | 2009-07-27 | 2016-11-23 | Lipoxen Technologies Limited | Glicopolisialilación de proteínas diferentes a proteínas de coagulación de la sangre |
KR101832937B1 (ko) | 2009-07-27 | 2018-02-28 | 박스알타 인코퍼레이티드 | 혈액 응고 단백질 복합체 |
SG10201401194VA (en) | 2009-07-27 | 2014-07-30 | Lipoxen Technologies Ltd | Glycopolysialylation of non-blood coagulation proteins |
US8642737B2 (en) | 2010-07-26 | 2014-02-04 | Baxter International Inc. | Nucleophilic catalysts for oxime linkage |
US9194011B2 (en) | 2009-11-17 | 2015-11-24 | Protalix Ltd. | Stabilized alpha-galactosidase and uses thereof |
CN101787117B (zh) * | 2010-02-08 | 2012-05-23 | 江南大学 | 聚乙二醇-聚唾液酸嵌段共聚物的制备方法及应用 |
JP2013533217A (ja) | 2010-05-17 | 2013-08-22 | セビックス・インコーポレイテッド | Peg化c−ペプチド |
WO2011156242A2 (en) * | 2010-06-11 | 2011-12-15 | Lpath, Inc. | Improved anti-lysophospholipid antibody design using antibody structures |
EP2598170A4 (en) | 2010-07-28 | 2016-07-06 | Smartcells Inc | MEDICAMENT-LIGAND CONJUGATES, THEIR SYNTHESIS AND CORRESPONDING INTERMEDIATES |
JP2013535467A (ja) | 2010-07-28 | 2013-09-12 | スマートセルズ・インコーポレイテツド | 組換えにより発現されたインスリンポリペプチドおよびその使用 |
JP2013541500A (ja) | 2010-07-28 | 2013-11-14 | スマートセルズ・インコーポレイテツド | 組換えレクチン、結合部位修飾レクチンおよびそれらの用途 |
EP2665814B1 (en) | 2011-01-20 | 2017-05-17 | Protalix Ltd. | Nucleic acid construct for expression of alpha-galactosidase in plants and plant cells |
WO2013075117A2 (en) | 2011-11-17 | 2013-05-23 | John Wahren | Pegylated c-peptide |
AU2014329567B2 (en) | 2013-10-04 | 2019-07-25 | Merck Sharp & Dohme Corp. | Glucose-responsive insulin conjugates |
WO2015130963A2 (en) | 2014-02-27 | 2015-09-03 | Xenetic Biosciences, Inc. | Compositions and methods for administering insulin or insulin-like protein to the brain |
JP2019218265A (ja) * | 2016-09-14 | 2019-12-26 | 生化学工業株式会社 | ペプチドの血中滞留性を増強させる方法 |
US20200179524A1 (en) * | 2017-04-25 | 2020-06-11 | Lipoxen Technologies Limited | Methods of treating multiple myeloma cancers expressing high levels of epo-receptor using psa-epo |
US20190083636A1 (en) * | 2017-04-25 | 2019-03-21 | Lipoxen Technologies Limited | Methods of treating diseases related to net formation with parenteral administration of polysialylated dnase i |
US20220023430A1 (en) * | 2018-11-13 | 2022-01-27 | Lipoxen Technologies Limited | Glycopolysialylation of blinatumomab |
EP3920956A4 (en) * | 2019-02-04 | 2022-11-16 | Xenetic Biosciences Inc. | METHODS OF USE OF GLYCOSYLATED THERAPEUTIC PROTEINS |
CN116249552A (zh) * | 2020-08-11 | 2023-06-09 | 隆延生物科技(上海)有限公司 | 一种液体制剂及其应用 |
CN114966021A (zh) * | 2022-05-19 | 2022-08-30 | 山东博科生物产业有限公司 | 一种稳定的脂蛋白相关磷脂酶a2测定试剂盒 |
Family Cites Families (56)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US4179337A (en) | 1973-07-20 | 1979-12-18 | Davis Frank F | Non-immunogenic polypeptides |
DE2930542A1 (de) | 1979-07-27 | 1981-02-12 | Hoechst Ag | Neue insulinderivate und verfahren zu ihrer herstellung |
US5308617A (en) * | 1988-08-10 | 1994-05-03 | Halzyme Ltd. | Protein heparin conjugates |
US7217689B1 (en) * | 1989-10-13 | 2007-05-15 | Amgen Inc. | Glycosylation analogs of erythropoietin |
WO1991005867A1 (en) | 1989-10-13 | 1991-05-02 | Amgen Inc. | Erythropoietin isoforms |
GB9112212D0 (en) | 1991-06-06 | 1991-07-24 | Gregoriadis Gregory | Pharmaceutical compositions |
US5846951A (en) * | 1991-06-06 | 1998-12-08 | The School Of Pharmacy, University Of London | Pharmaceutical compositions |
NO924985L (no) | 1991-12-30 | 1993-07-01 | Akzo Nv | Thyroaktiv blanding med vedvarende frigjoering |
JP2747967B2 (ja) * | 1993-07-23 | 1998-05-06 | 雪印乳業株式会社 | シアル酸粉末 |
US20030053982A1 (en) | 1994-09-26 | 2003-03-20 | Kinstler Olaf B. | N-terminally chemically modified protein compositions and methods |
US5824784A (en) * | 1994-10-12 | 1998-10-20 | Amgen Inc. | N-terminally chemically modified protein compositions and methods |
ATE227996T1 (de) * | 1997-08-05 | 2002-12-15 | Bioniche Life Sciences Inc | Zusammensetzung und verfahren zur regulierung von zellproliferation und zelltod |
WO1999043307A1 (en) | 1998-02-26 | 1999-09-02 | Prange Arthur J Jr | Thyroid hormone replacement using sustained release triiodothyronine |
RU2141531C1 (ru) | 1999-05-26 | 1999-11-20 | Российское акционерное общество открытого типа "Биопрепарат" | Способ получения рекомбинантного инсулина человека |
US6323311B1 (en) | 1999-09-22 | 2001-11-27 | University Of Utah Research Foundation | Synthesis of insulin derivatives |
EP1335931B1 (en) | 2000-05-16 | 2005-12-21 | Lipoxen Technologies Limited | Derivatisation of proteins in aqueous solution |
WO2001087272A2 (en) | 2000-05-18 | 2001-11-22 | Therics, Inc. | Encapsulating a toxic core within a non-toxic region in an oral dosage form |
US7118737B2 (en) * | 2000-09-08 | 2006-10-10 | Amylin Pharmaceuticals, Inc. | Polymer-modified synthetic proteins |
JP5170931B2 (ja) | 2000-10-16 | 2013-03-27 | 中外製薬株式会社 | Peg修飾エリスロポエチン |
AU3323002A (en) | 2000-12-20 | 2002-07-01 | Hoffmann La Roche | Erythropoietin conjugates |
KR100401296B1 (ko) | 2000-12-27 | 2003-10-11 | 드림바이오젠 주식회사 | 수식물질에 의해 수식된 단백질 변이체 및 이것의 제조방법 |
US7125843B2 (en) * | 2001-10-19 | 2006-10-24 | Neose Technologies, Inc. | Glycoconjugates including more than one peptide |
CN102180944A (zh) * | 2001-10-10 | 2011-09-14 | 诺和诺德公司 | 肽的重构和糖缀合 |
AU2002351746A1 (en) | 2001-12-21 | 2003-07-15 | Maxygen Aps | Erythropoietin conjugates |
ITPD20010302A1 (it) | 2001-12-28 | 2003-06-28 | Bbs Riva Spa | Dispositivo idraulico per pompare e / p intercettare metallo allo stato fuso |
US6763226B1 (en) | 2002-07-31 | 2004-07-13 | Computer Science Central, Inc. | Multifunctional world wide walkie talkie, a tri-frequency cellular-satellite wireless instant messenger computer and network for establishing global wireless volp quality of service (qos) communications, unified messaging, and video conferencing via the internet |
EP1681303B1 (en) | 2002-09-11 | 2013-09-04 | Fresenius Kabi Deutschland GmbH | HASylated polypeptides, especially HASylated erythropoietin |
EP1400533A1 (en) * | 2002-09-11 | 2004-03-24 | Fresenius Kabi Deutschland GmbH | HASylated polypeptides, especially HASylated erythropoietin |
BR0314107A (pt) * | 2002-09-11 | 2005-07-19 | Fresenius Kabi De Gmbh | Método de produção de derivados de hidroxialquil amido |
CN1777440A (zh) | 2003-04-11 | 2006-05-24 | Pr药品有限公司 | 位点特异性蛋白质偶联物的制备方法 |
WO2004101619A1 (ja) | 2003-05-15 | 2004-11-25 | Shionogi Co., Ltd. | 機能的糖ペプチドの合理的設計および合成 |
US7074755B2 (en) * | 2003-05-17 | 2006-07-11 | Centocor, Inc. | Erythropoietin conjugate compounds with extended half-lives |
DE602004016170D1 (de) | 2003-07-03 | 2008-10-09 | Cipla Ltd | Verfahren zur herstellung von finasterid form i |
EP1651547B1 (en) | 2003-08-05 | 2006-11-22 | Dematic Corp. | Motorized roller transverse drive |
AU2004281630A1 (en) * | 2003-08-06 | 2005-04-28 | Bio-Manguinhos/Fiocruz | Process for preparing polysaccharide-protein conjugate vaccines |
EP1660134B1 (en) | 2003-08-08 | 2010-12-29 | Fresenius Kabi Deutschland GmbH | Conjugates of hydroxyalkyl starch and g-csf |
RU2333223C2 (ru) | 2003-08-12 | 2008-09-10 | Лайпоксен Текнолоджиз Лимитед | Альдегидные производные сиаловой кислоты, способы их получения, конъюгаты альдегидных производных сиаловой кислоты и фармацевтическая композиция на их основе |
ES2294535T3 (es) | 2003-08-12 | 2008-04-01 | Lipoxen Technologies Limited | Derivados del acido polisialico. |
US7405198B2 (en) * | 2003-11-24 | 2008-07-29 | Neose Technologies, Inc. | Glycopegylated erythropoietin |
KR101237884B1 (ko) * | 2003-12-03 | 2013-02-27 | 바이오제너릭스 에이지 | 글리코 peg화 과립구 콜로니 자극인자 |
US7956032B2 (en) | 2003-12-03 | 2011-06-07 | Novo Nordisk A/S | Glycopegylated granulocyte colony stimulating factor |
AR048035A1 (es) * | 2004-03-11 | 2006-03-22 | Fresenius Kabi De Gmbh | Conjugados de almidon de hidroxialquilo y una proteina, preparados por aminacion reductora |
FR2868071B1 (fr) * | 2004-03-26 | 2006-06-09 | Biomerieux Sa | Reactifs de marquage, procedes de synthese de tels reactifs et procedes de detection de molecules biologiques |
DE102004030392A1 (de) | 2004-06-23 | 2006-01-19 | Endress + Hauser Flowtec Ag, Reinach | Meßwandler vom Vibrationstyp |
WO2006014148A2 (fr) | 2004-08-04 | 2006-02-09 | Sergey Alexandrovich Orlov | Procede permettant d'organiser un processus de jeu a action intermittente |
GB2416993A (en) | 2004-08-11 | 2006-02-15 | Dinesh Verma | Opthalmic prosthesis |
US8652334B2 (en) | 2004-08-12 | 2014-02-18 | Lipoxen Technologies Limited | Fractionation of charged polysaccharide |
ES2593318T3 (es) * | 2004-08-12 | 2016-12-07 | Lipoxen Technologies Limited | Derivados de ácido siálico |
EP1858543B1 (en) | 2005-01-10 | 2013-11-27 | BioGeneriX AG | Glycopegylated granulocyte colony stimulating factor |
TWI376234B (en) * | 2005-02-01 | 2012-11-11 | Msd Oss Bv | Conjugates of a polypeptide and an oligosaccharide |
CN101160326B (zh) | 2005-02-23 | 2013-04-10 | 利普生技术有限公司 | 用于蛋白质衍生和缀合的活化的唾液酸衍生物 |
JP3989936B2 (ja) * | 2005-04-07 | 2007-10-10 | 進 須永 | 抗腫瘍剤及び新規dnアーゼ |
US20070099820A1 (en) | 2005-10-19 | 2007-05-03 | Smartcells, Inc. | Polymer-drug conjugates |
ES2569066T3 (es) * | 2006-07-25 | 2016-05-06 | Lipoxen Technologies Limited | Conjugación N-terminal de ácido polisiálico a proteínas |
US8933025B2 (en) | 2009-07-16 | 2015-01-13 | Kao Corporation | Agent for suppressing postprandial elevation of blood insulin concentration |
TWI593708B (zh) | 2011-09-26 | 2017-08-01 | 諾華公司 | 治療代謝病症之融合蛋白質 |
-
2007
- 2007-07-25 ES ES07766361.5T patent/ES2569066T3/es active Active
- 2007-07-25 CN CN201310022631.9A patent/CN103169984B/zh not_active Expired - Fee Related
- 2007-07-25 US US12/375,012 patent/US8394921B2/en active Active
- 2007-07-25 JP JP2009521342A patent/JP2009544680A/ja active Pending
- 2007-07-25 ES ES07789047T patent/ES2344670T3/es active Active
- 2007-07-25 RU RU2009105696/15A patent/RU2432175C2/ru active
- 2007-07-25 JP JP2009521336A patent/JP5419689B2/ja not_active Expired - Fee Related
- 2007-07-25 US US12/375,006 patent/US8299015B2/en active Active
- 2007-07-25 WO PCT/GB2007/002839 patent/WO2008012540A1/en active Application Filing
- 2007-07-25 EP EP13163525.2A patent/EP2630972B1/en not_active Not-in-force
- 2007-07-25 ES ES07789051.5T patent/ES2581902T3/es active Active
- 2007-07-25 ES ES13163525.2T patent/ES2647528T3/es active Active
- 2007-07-25 AT AT07789047T patent/ATE467642T1/de not_active IP Right Cessation
- 2007-07-25 DE DE602007006492T patent/DE602007006492D1/de active Active
- 2007-07-25 WO PCT/GB2007/002841 patent/WO2008012542A2/en active Application Filing
- 2007-07-25 US US12/375,010 patent/US10300144B2/en active Active
- 2007-07-25 WO PCT/GB2007/002816 patent/WO2008012525A1/en active Application Filing
- 2007-07-25 JP JP2009521337A patent/JP5096466B2/ja active Active
- 2007-07-25 US US12/375,008 patent/US8299026B2/en active Active
- 2007-07-25 EP EP07789047A patent/EP2041167B1/en not_active Not-in-force
- 2007-07-25 EP EP07789051.5A patent/EP2043693B1/en not_active Not-in-force
- 2007-07-25 EP EP17188428.1A patent/EP3299033A1/en not_active Withdrawn
- 2007-07-25 CN CN2007800337418A patent/CN101511391B/zh not_active Expired - Fee Related
- 2007-07-25 ES ES07766363.1T patent/ES2581983T3/es active Active
- 2007-07-25 WO PCT/GB2007/002821 patent/WO2008012528A1/en active Application Filing
- 2007-07-25 EP EP07766363.1A patent/EP2043692B1/en not_active Not-in-force
- 2007-07-25 EP EP07766361.5A patent/EP2043616B1/en not_active Not-in-force
- 2007-07-25 KR KR1020097003805A patent/KR101400105B1/ko active IP Right Grant
- 2007-07-25 JP JP2009521343A patent/JP2009544681A/ja active Pending
-
2012
- 2012-09-19 JP JP2012205475A patent/JP5586669B2/ja not_active Expired - Fee Related
- 2012-10-05 US US13/646,605 patent/US8796207B2/en active Active
- 2012-10-05 US US13/646,584 patent/US9040478B2/en active Active
- 2012-12-28 JP JP2012287324A patent/JP5542195B2/ja active Active
-
2013
- 2013-02-08 JP JP2013022825A patent/JP5420091B2/ja active Active
- 2013-03-11 US US13/794,692 patent/US8981050B2/en active Active
- 2013-08-01 JP JP2013160269A patent/JP5941440B2/ja active Active
-
2014
- 2014-02-13 JP JP2014025061A patent/JP6165079B2/ja active Active
- 2014-06-24 US US14/313,870 patent/US8933026B2/en active Active
- 2014-06-24 US US14/313,897 patent/US8946406B2/en not_active Expired - Fee Related
- 2014-06-24 US US14/313,888 patent/US9266936B2/en active Active
- 2014-07-29 JP JP2014154037A patent/JP5912152B2/ja active Active
- 2014-12-05 US US14/561,991 patent/US9234020B2/en active Active
-
2015
- 2015-02-04 US US14/614,406 patent/US9492556B2/en active Active
- 2015-04-01 JP JP2015075148A patent/JP6055506B2/ja active Active
- 2015-04-17 US US14/689,627 patent/US9492557B2/en active Active
- 2015-05-22 US US14/720,700 patent/US9474805B2/en active Active
-
2016
- 2016-01-19 US US15/001,135 patent/US9579393B2/en active Active
- 2016-01-19 US US15/001,144 patent/US9549990B2/en active Active
- 2016-02-05 JP JP2016020557A patent/JP6243456B2/ja active Active
- 2016-07-29 JP JP2016149090A patent/JP6203342B2/ja active Active
- 2016-10-03 US US15/284,426 patent/US20170080054A1/en not_active Abandoned
- 2016-11-15 US US15/352,466 patent/US9789163B2/en active Active
-
2017
- 2017-01-12 US US15/404,896 patent/US20170119893A1/en not_active Abandoned
- 2017-08-18 JP JP2017157728A patent/JP6581157B2/ja active Active
- 2017-11-13 US US15/811,050 patent/US20180289823A1/en not_active Abandoned
-
2019
- 2019-03-27 US US16/367,226 patent/US20190216938A1/en not_active Abandoned
-
2022
- 2022-01-14 US US17/576,821 patent/US20220133898A1/en active Pending
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
RU2472806C1 (ru) * | 2008-10-20 | 2013-01-20 | Юсв Лимитед | Усовершенствованный способ пегилирования белков |
Also Published As
Similar Documents
Publication | Publication Date | Title |
---|---|---|
RU2009105696A (ru) | N-концевое полисиалилирование | |
JP4482267B2 (ja) | 接合安定化されたポリペプチド組成物 | |
Parsons et al. | Oligosaccharide moieties of glycoprotein hormones: bovine lutropin resists enzymatic deglycosylation because of terminal O-sulfated N-acetylhexosamines. | |
BE1004357A4 (fr) | Nouveaux derives peptidiques, leur preparation et leur utilisation comme medicaments. | |
EP0140084B1 (de) | Verfahren zur Herstellung von Insulin-Derivaten, deren B-Kette C-terminal verlängert ist, neue basisch modifizierte Insulin-Derivate, diese enthaltende Mittel und ihre Verwendung | |
US9040660B2 (en) | Long-acting gastrin derivatives | |
Otvos Jr et al. | Automated solid-phase synthesis of glycopeptides. Incorporation of unprotected mono-and disaccharide units of N-glycoprotein antennae into T cell epitopic peptides | |
BRPI0607248A2 (pt) | conjugado de um polipeptìdeo e um oligossacarìdeo, composição farmacêutica, uso do conjugado, e, processo para a preparação de um conjugado | |
UA89616C2 (ru) | Гидролизат казеина, способ его получения и применения | |
JP2005527470A5 (ru) | ||
WO2004100997A2 (en) | Spacer moiety for poly(ethylene glycol) -modified peptides | |
BR0008759A (pt) | Métodos para a produção de proteinas contendo resìduos de cisteina livre | |
WO2012158964A2 (en) | Improved peptide pharmaceuticals for osteoporosis | |
JPS61178926A (ja) | 化学修飾ペプチドホルモンおよびその製造法 | |
DE10207072A1 (de) | Stärkederivate, ihre Konjugate und Verfahren zur Herstellung derselben | |
GB0310919D0 (en) | Pharmaceutical compositions | |
JPH02131594A (ja) | デ‐b30‐インシュリンおよびデ‐b30‐インシュリン誘導体の製造方法 | |
ES8501364A1 (es) | Un metodo para la preparacion de nuevos polipeptidos. | |
FI79860B (fi) | Foerfarande foer framstaellning av humaninsulin des-pheb1-humaninsulin eller derivat daerav ur svininsulin, des-pheb1-svininsulin eller derivat daerav. | |
FI78119C (fi) | Foerfarande foer framstaellning av maenskligt insulin eller b-30-estrar daerav. | |
KR850001775A (ko) | 인슐린 유도체의 제조방법 | |
DK172712B1 (da) | Fremgangsmåde til udvinding af insulin-forløbere fra reaktionsblandinger, der fremkommer ved foldning af insulin-forløbere | |
KR970703307A (ko) | 아미노술폰산 유도체, 의사펩티드 합성으로의 용도 및 이들의 제조 방법(derivatives of aminosulfonic acids, utilization of the same in the synthesis of pseudopeptides and process for their preparation) | |
JPS5950315B2 (ja) | ポリペプチドの製法 | |
RU95100762A (ru) | Способ получения n-бензилоксикарбонил- альфа - l-аспартил-l-фенилаланин метилового эфира |