AU2002214466A1 - Oral pharmaceutical composition containing a block copolymer - Google Patents
Oral pharmaceutical composition containing a block copolymerInfo
- Publication number
- AU2002214466A1 AU2002214466A1 AU2002214466A AU1446602A AU2002214466A1 AU 2002214466 A1 AU2002214466 A1 AU 2002214466A1 AU 2002214466 A AU2002214466 A AU 2002214466A AU 1446602 A AU1446602 A AU 1446602A AU 2002214466 A1 AU2002214466 A1 AU 2002214466A1
- Authority
- AU
- Australia
- Prior art keywords
- copolymer
- pharmaceutical composition
- poly
- oral pharmaceutical
- compound
- 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
- 239000008203 oral pharmaceutical composition Substances 0.000 title claims abstract description 22
- 229920001400 block copolymer Polymers 0.000 title claims abstract description 15
- 229920001577 copolymer Polymers 0.000 claims abstract description 46
- 150000001875 compounds Chemical class 0.000 claims abstract description 32
- JVTAAEKCZFNVCJ-UHFFFAOYSA-N lactic acid Chemical compound CC(O)C(O)=O JVTAAEKCZFNVCJ-UHFFFAOYSA-N 0.000 claims abstract description 20
- 239000000693 micelle Substances 0.000 claims abstract description 20
- 229920001223 polyethylene glycol Polymers 0.000 claims abstract description 20
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims abstract description 19
- -1 poly(L-lactide) Polymers 0.000 claims abstract description 18
- 229920000359 diblock copolymer Polymers 0.000 claims abstract description 14
- 239000002202 Polyethylene glycol Substances 0.000 claims abstract description 11
- 229960000448 lactic acid Drugs 0.000 claims abstract description 10
- 229920000428 triblock copolymer Polymers 0.000 claims abstract description 8
- 229920006030 multiblock copolymer Polymers 0.000 claims abstract description 6
- 229920000642 polymer Polymers 0.000 claims description 27
- 239000000203 mixture Substances 0.000 claims description 22
- 229920001983 poloxamer Polymers 0.000 claims description 12
- 238000001179 sorption measurement Methods 0.000 claims description 12
- 229920003171 Poly (ethylene oxide) Polymers 0.000 claims description 10
- 229920001477 hydrophilic polymer Polymers 0.000 claims description 10
- JJTUDXZGHPGLLC-UHFFFAOYSA-N lactide Chemical compound CC1OC(=O)C(C)OC1=O JJTUDXZGHPGLLC-UHFFFAOYSA-N 0.000 claims description 8
- AEMRFAOFKBGASW-UHFFFAOYSA-N Glycolic acid Polymers OCC(O)=O AEMRFAOFKBGASW-UHFFFAOYSA-N 0.000 claims description 5
- 229920000954 Polyglycolide Polymers 0.000 claims description 5
- 239000004372 Polyvinyl alcohol Substances 0.000 claims description 5
- 229920001610 polycaprolactone Polymers 0.000 claims description 5
- 239000004633 polyglycolic acid Substances 0.000 claims description 5
- 229950008885 polyglycolic acid Drugs 0.000 claims description 5
- 229920001451 polypropylene glycol Polymers 0.000 claims description 5
- 229920002451 polyvinyl alcohol Polymers 0.000 claims description 5
- 235000019422 polyvinyl alcohol Nutrition 0.000 claims description 5
- 229920000036 polyvinylpyrrolidone Polymers 0.000 claims description 5
- 239000001267 polyvinylpyrrolidone Substances 0.000 claims description 5
- 235000013855 polyvinylpyrrolidone Nutrition 0.000 claims description 5
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 claims description 4
- GLUUGHFHXGJENI-UHFFFAOYSA-N Piperazine Chemical compound C1CNCCN1 GLUUGHFHXGJENI-UHFFFAOYSA-N 0.000 claims description 4
- 125000003236 benzoyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C(*)=O 0.000 claims description 2
- WGCNASOHLSPBMP-UHFFFAOYSA-N hydroxyacetaldehyde Natural products OCC=O WGCNASOHLSPBMP-UHFFFAOYSA-N 0.000 claims description 2
- 229920001432 poly(L-lactide) Polymers 0.000 abstract 1
- 229940125904 compound 1 Drugs 0.000 description 18
- 229940079593 drug Drugs 0.000 description 16
- 239000003814 drug Substances 0.000 description 16
- 238000009472 formulation Methods 0.000 description 11
- 238000000034 method Methods 0.000 description 9
- 229920000747 poly(lactic acid) Polymers 0.000 description 9
- 239000007962 solid dispersion Substances 0.000 description 9
- 210000002784 stomach Anatomy 0.000 description 8
- 238000010521 absorption reaction Methods 0.000 description 7
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 6
- 238000001556 precipitation Methods 0.000 description 5
- 239000002904 solvent Substances 0.000 description 5
- 239000000725 suspension Substances 0.000 description 5
- 239000000546 pharmaceutical excipient Substances 0.000 description 4
- YMWUJEATGCHHMB-UHFFFAOYSA-N Dichloromethane Chemical compound ClCCl YMWUJEATGCHHMB-UHFFFAOYSA-N 0.000 description 3
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 3
- 230000015572 biosynthetic process Effects 0.000 description 3
- 210000001072 colon Anatomy 0.000 description 3
- 229940125782 compound 2 Drugs 0.000 description 3
- 229940126214 compound 3 Drugs 0.000 description 3
- 238000004090 dissolution Methods 0.000 description 3
- 238000011978 dissolution method Methods 0.000 description 3
- 210000001198 duodenum Anatomy 0.000 description 3
- 238000001704 evaporation Methods 0.000 description 3
- 210000003405 ileum Anatomy 0.000 description 3
- 238000002360 preparation method Methods 0.000 description 3
- 230000002265 prevention Effects 0.000 description 3
- 210000000813 small intestine Anatomy 0.000 description 3
- 239000000243 solution Substances 0.000 description 3
- 206010053567 Coagulopathies Diseases 0.000 description 2
- 239000007836 KH2PO4 Substances 0.000 description 2
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 2
- 230000002378 acidificating effect Effects 0.000 description 2
- 150000007514 bases Chemical class 0.000 description 2
- 230000008901 benefit Effects 0.000 description 2
- 208000026106 cerebrovascular disease Diseases 0.000 description 2
- 230000035602 clotting Effects 0.000 description 2
- 210000004351 coronary vessel Anatomy 0.000 description 2
- 238000001514 detection method Methods 0.000 description 2
- 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 description 2
- 208000035475 disorder Diseases 0.000 description 2
- 238000007922 dissolution test Methods 0.000 description 2
- 230000000694 effects Effects 0.000 description 2
- 239000012530 fluid Substances 0.000 description 2
- 210000001035 gastrointestinal tract Anatomy 0.000 description 2
- 239000007903 gelatin capsule Substances 0.000 description 2
- 238000004128 high performance liquid chromatography Methods 0.000 description 2
- 238000009474 hot melt extrusion Methods 0.000 description 2
- 238000000338 in vitro Methods 0.000 description 2
- 239000000155 melt Substances 0.000 description 2
- 229910000402 monopotassium phosphate Inorganic materials 0.000 description 2
- 229920003023 plastic Polymers 0.000 description 2
- 239000004033 plastic Substances 0.000 description 2
- GNSKLFRGEWLPPA-UHFFFAOYSA-M potassium dihydrogen phosphate Chemical compound [K+].OP(O)([O-])=O GNSKLFRGEWLPPA-UHFFFAOYSA-M 0.000 description 2
- 238000005070 sampling Methods 0.000 description 2
- 238000001356 surgical procedure Methods 0.000 description 2
- 206010002383 Angina Pectoris Diseases 0.000 description 1
- 206010002388 Angina unstable Diseases 0.000 description 1
- 206010003178 Arterial thrombosis Diseases 0.000 description 1
- 208000037260 Atherosclerotic Plaque Diseases 0.000 description 1
- 206010008088 Cerebral artery embolism Diseases 0.000 description 1
- 206010008132 Cerebral thrombosis Diseases 0.000 description 1
- 108010074860 Factor Xa Proteins 0.000 description 1
- 229940123583 Factor Xa inhibitor Drugs 0.000 description 1
- 244000287680 Garcinia dulcis Species 0.000 description 1
- 201000001429 Intracranial Thrombosis Diseases 0.000 description 1
- RVGRUAULSDPKGF-UHFFFAOYSA-N Poloxamer Chemical compound C1CO1.CC1CO1 RVGRUAULSDPKGF-UHFFFAOYSA-N 0.000 description 1
- 208000010378 Pulmonary Embolism Diseases 0.000 description 1
- 206010038563 Reocclusion Diseases 0.000 description 1
- 208000006011 Stroke Diseases 0.000 description 1
- 108090000190 Thrombin Proteins 0.000 description 1
- 208000007536 Thrombosis Diseases 0.000 description 1
- 208000007814 Unstable Angina Diseases 0.000 description 1
- 208000024248 Vascular System injury Diseases 0.000 description 1
- 208000012339 Vascular injury Diseases 0.000 description 1
- 206010047249 Venous thrombosis Diseases 0.000 description 1
- 238000002399 angioplasty Methods 0.000 description 1
- 230000000181 anti-adherent effect Effects 0.000 description 1
- 239000003911 antiadherent Substances 0.000 description 1
- 239000003146 anticoagulant agent Substances 0.000 description 1
- 229940127219 anticoagulant drug Drugs 0.000 description 1
- 239000003963 antioxidant agent Substances 0.000 description 1
- 230000003078 antioxidant effect Effects 0.000 description 1
- 235000006708 antioxidants Nutrition 0.000 description 1
- 239000008280 blood Substances 0.000 description 1
- 210000004369 blood Anatomy 0.000 description 1
- 230000023555 blood coagulation Effects 0.000 description 1
- 210000004204 blood vessel Anatomy 0.000 description 1
- 239000002775 capsule Substances 0.000 description 1
- 206010008118 cerebral infarction Diseases 0.000 description 1
- 238000012512 characterization method Methods 0.000 description 1
- 230000015271 coagulation Effects 0.000 description 1
- 238000005345 coagulation Methods 0.000 description 1
- 238000007906 compression Methods 0.000 description 1
- 230000006835 compression Effects 0.000 description 1
- 208000029078 coronary artery disease Diseases 0.000 description 1
- 230000007423 decrease Effects 0.000 description 1
- 230000002526 effect on cardiovascular system Effects 0.000 description 1
- 239000003480 eluent Substances 0.000 description 1
- 239000003623 enhancer Substances 0.000 description 1
- 230000002708 enhancing effect Effects 0.000 description 1
- 230000002255 enzymatic effect Effects 0.000 description 1
- 230000008020 evaporation Effects 0.000 description 1
- 238000004108 freeze drying Methods 0.000 description 1
- 238000002682 general surgery Methods 0.000 description 1
- 238000000227 grinding Methods 0.000 description 1
- 210000003709 heart valve Anatomy 0.000 description 1
- 238000011540 hip replacement Methods 0.000 description 1
- 239000003112 inhibitor Substances 0.000 description 1
- 230000002401 inhibitory effect Effects 0.000 description 1
- 230000005764 inhibitory process Effects 0.000 description 1
- 238000002347 injection Methods 0.000 description 1
- 239000007924 injection Substances 0.000 description 1
- 201000004332 intermediate coronary syndrome Diseases 0.000 description 1
- 201000010849 intracranial embolism Diseases 0.000 description 1
- 208000028867 ischemia Diseases 0.000 description 1
- 230000014759 maintenance of location Effects 0.000 description 1
- 239000011159 matrix material Substances 0.000 description 1
- 238000005259 measurement Methods 0.000 description 1
- 238000002156 mixing Methods 0.000 description 1
- 208000010125 myocardial infarction Diseases 0.000 description 1
- AICOOMRHRUFYCM-ZRRPKQBOSA-N oxazine, 1 Chemical compound C([C@@H]1[C@H](C(C[C@]2(C)[C@@H]([C@H](C)N(C)C)[C@H](O)C[C@]21C)=O)CC1=CC2)C[C@H]1[C@@]1(C)[C@H]2N=C(C(C)C)OC1 AICOOMRHRUFYCM-ZRRPKQBOSA-N 0.000 description 1
- 230000000704 physical effect Effects 0.000 description 1
- 239000004014 plasticizer Substances 0.000 description 1
- 229920001993 poloxamer 188 Polymers 0.000 description 1
- 229920001992 poloxamer 407 Polymers 0.000 description 1
- 239000003755 preservative agent Substances 0.000 description 1
- 230000002035 prolonged effect Effects 0.000 description 1
- 208000037803 restenosis Diseases 0.000 description 1
- 238000002390 rotary evaporation Methods 0.000 description 1
- 239000000377 silicon dioxide Substances 0.000 description 1
- 238000001694 spray drying Methods 0.000 description 1
- 239000003381 stabilizer Substances 0.000 description 1
- 208000011580 syndromic disease Diseases 0.000 description 1
- 239000007916 tablet composition Substances 0.000 description 1
- 230000001225 therapeutic effect Effects 0.000 description 1
- 238000002560 therapeutic procedure Methods 0.000 description 1
- 239000010409 thin film Substances 0.000 description 1
- 230000001732 thrombotic effect Effects 0.000 description 1
Classifications
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K9/00—Medicinal preparations characterised by special physical form
- A61K9/10—Dispersions; Emulsions
- A61K9/107—Emulsions ; Emulsion preconcentrates; Micelles
- A61K9/1075—Microemulsions or submicron emulsions; Preconcentrates or solids thereof; Micelles, e.g. made of phospholipids or block copolymers
-
- 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
- A61K47/30—Macromolecular organic or inorganic compounds, e.g. inorganic polyphosphates
- A61K47/34—Macromolecular compounds obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds, e.g. polyesters, polyamino acids, polysiloxanes, polyphosphazines, copolymers of polyalkylene glycol or poloxamers
-
- 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
- A61P7/02—Antithrombotic agents; Anticoagulants; Platelet aggregation inhibitors
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P9/00—Drugs for disorders of the cardiovascular system
- A61P9/10—Drugs for disorders of the cardiovascular system for treating ischaemic or atherosclerotic diseases, e.g. antianginal drugs, coronary vasodilators, drugs for myocardial infarction, retinopathy, cerebrovascula insufficiency, renal arteriosclerosis
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K9/00—Medicinal preparations characterised by special physical form
- A61K9/14—Particulate form, e.g. powders, Processes for size reducing of pure drugs or the resulting products, Pure drug nanoparticles
- A61K9/141—Intimate drug-carrier mixtures characterised by the carrier, e.g. ordered mixtures, adsorbates, solid solutions, eutectica, co-dried, co-solubilised, co-kneaded, co-milled, co-ground products, co-precipitates, co-evaporates, co-extrudates, co-melts; Drug nanoparticles with adsorbed surface modifiers
- A61K9/146—Intimate drug-carrier mixtures characterised by the carrier, e.g. ordered mixtures, adsorbates, solid solutions, eutectica, co-dried, co-solubilised, co-kneaded, co-milled, co-ground products, co-precipitates, co-evaporates, co-extrudates, co-melts; Drug nanoparticles with adsorbed surface modifiers with organic macromolecular compounds
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K9/00—Medicinal preparations characterised by special physical form
- A61K9/48—Preparations in capsules, e.g. of gelatin, of chocolate
- A61K9/4841—Filling excipients; Inactive ingredients
- A61K9/4866—Organic macromolecular compounds
Landscapes
- Health & Medical Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Pharmacology & Pharmacy (AREA)
- Veterinary Medicine (AREA)
- Public Health (AREA)
- General Health & Medical Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- Medicinal Chemistry (AREA)
- Engineering & Computer Science (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Epidemiology (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Biophysics (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- General Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Dispersion Chemistry (AREA)
- Molecular Biology (AREA)
- Diabetes (AREA)
- Inorganic Chemistry (AREA)
- Cardiology (AREA)
- Urology & Nephrology (AREA)
- Heart & Thoracic Surgery (AREA)
- Hematology (AREA)
- Proteomics, Peptides & Aminoacids (AREA)
- Vascular Medicine (AREA)
- Medicinal Preparation (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
- Pyridine Compounds (AREA)
- Plural Heterocyclic Compounds (AREA)
- Compositions Of Macromolecular Compounds (AREA)
Applications Claiming Priority (5)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| GB0027375A GB0027375D0 (en) | 2000-11-09 | 2000-11-09 | Pharmaceutical composition |
| GB0027375 | 2000-11-09 | ||
| GB0104751 | 2001-02-27 | ||
| GB0104751A GB0104751D0 (en) | 2001-02-27 | 2001-02-27 | Pharmaceutical composition |
| PCT/SE2001/002470 WO2002038184A1 (fr) | 2000-11-09 | 2001-11-07 | Composition pharmaceutique administree par voie orale contenant un copolymere sequence |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| AU2002214466A1 true AU2002214466A1 (en) | 2002-05-21 |
Family
ID=26245262
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| AU2002214466A Abandoned AU2002214466A1 (en) | 2000-11-09 | 2001-11-07 | Oral pharmaceutical composition containing a block copolymer |
Country Status (20)
| Country | Link |
|---|---|
| US (1) | US20040076673A1 (fr) |
| EP (1) | EP1343530B1 (fr) |
| JP (1) | JP4255692B2 (fr) |
| KR (1) | KR20030057549A (fr) |
| CN (1) | CN100408099C (fr) |
| AT (1) | ATE369151T1 (fr) |
| AU (1) | AU2002214466A1 (fr) |
| BR (1) | BR0115204A (fr) |
| CA (1) | CA2428784A1 (fr) |
| CY (1) | CY1106908T1 (fr) |
| DE (1) | DE60129838T2 (fr) |
| DK (1) | DK1343530T3 (fr) |
| ES (1) | ES2289002T3 (fr) |
| HK (1) | HK1061646A1 (fr) |
| IL (1) | IL155691A0 (fr) |
| MX (1) | MXPA03004112A (fr) |
| NO (1) | NO20032070L (fr) |
| NZ (1) | NZ525726A (fr) |
| PT (1) | PT1343530E (fr) |
| WO (1) | WO2002038184A1 (fr) |
Families Citing this family (24)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE10026698A1 (de) | 2000-05-30 | 2001-12-06 | Basf Ag | Selbstemulgierende Wirkstoffformulierung und Verwendung dieser Formulierung |
| ATE380834T1 (de) * | 2002-05-03 | 2007-12-15 | Janssen Pharmaceutica Nv | Polymermikroemulsionen |
| KR100502840B1 (ko) * | 2002-09-04 | 2005-07-21 | 학교법인 포항공과대학교 | 약물 담지능력이 우수한 블록 공중합체 미셀 조성물 |
| US7263401B2 (en) * | 2003-05-16 | 2007-08-28 | Medtronic, Inc. | Implantable medical device with a nonhermetic battery |
| US8025899B2 (en) | 2003-08-28 | 2011-09-27 | Abbott Laboratories | Solid pharmaceutical dosage form |
| US8377952B2 (en) | 2003-08-28 | 2013-02-19 | Abbott Laboratories | Solid pharmaceutical dosage formulation |
| US20060224095A1 (en) * | 2005-04-05 | 2006-10-05 | University Of New Hampshire | Biocompatible polymeric vesicles self assembled from triblock copolymers |
| WO2006109945A1 (fr) * | 2005-04-13 | 2006-10-19 | Sungkyunkwan University Foundation For Corporate Collaboration | Copolymere bloc sensible a la temperature et au ph, et hydrogels polymere l'utilisant |
| KR100665672B1 (ko) * | 2005-04-13 | 2007-01-09 | 성균관대학교산학협력단 | 새로운 온도 및 ｐＨ 민감성 블록 공중합체 및 이를 이용한고분자 하이드로겔 |
| CN100334219C (zh) * | 2005-05-12 | 2007-08-29 | 华中科技大学同济医学院附属同济医院 | 共聚物促进超声介导基因转染的方法 |
| CN101400717B (zh) * | 2006-03-09 | 2011-08-31 | 科洛普拉斯特公司 | 具有用于软组织再生的改进生物相容性的可降解亲水嵌段共聚物 |
| US8871242B2 (en) | 2006-11-17 | 2014-10-28 | National Cerebral And Cardiovascular Center | Blood anticoagulant material, coating material and indwelling device comprising the same, and treatment using blood anticoagulant material |
| KR100949850B1 (ko) * | 2007-11-16 | 2010-03-29 | 성균관대학교산학협력단 | 약물방출성이 우수한 온도 및 피에치 민감성 블록공중합체및 이의 제조방법과 이를 이용한 약물전달체 |
| WO2009104706A1 (fr) | 2008-02-22 | 2009-08-27 | 東レ株式会社 | Microparticules et leurs compositions pharmaceutiques |
| CN101732724B (zh) * | 2010-01-07 | 2012-04-25 | 浙江大学 | 一种携载抗肿瘤药物的复合胶束及其制备方法 |
| CN101899146B (zh) * | 2010-07-28 | 2012-04-18 | 重庆大学 | 一种基于哌嗪嵌段端羟基聚酯类材料及其制备方法 |
| CN101982168B (zh) * | 2010-11-02 | 2012-05-23 | 山东大学 | 一种槲皮素纳米胶束制剂及其制备方法 |
| CN102935062B (zh) * | 2011-08-16 | 2014-10-15 | 王成 | 负载埃坡霉素类化合物或其衍生物的聚合物胶束组合物、冻干制剂的制备及应用 |
| TWI641396B (zh) | 2011-09-23 | 2018-11-21 | Bvw控股公司 | 醫療共聚物 |
| WO2014001905A1 (fr) * | 2012-06-27 | 2014-01-03 | Medincell | Administration de médicament biodégradable pour compositions hydrophobes |
| CN103006557A (zh) * | 2012-11-29 | 2013-04-03 | 中国人民解放军军事医学科学院毒物药物研究所 | 丝裂霉素a胶束制剂、其制备方法及用途 |
| WO2014176578A1 (fr) | 2013-04-25 | 2014-10-30 | A.R. Arena Products, Inc. | Contenant de fromage pouvant etre desassemble ayant un dispositif de verrouillage enveloppant et un volume de remplissage accru |
| CN105902515B (zh) * | 2016-05-19 | 2019-04-05 | 宁波盖济尔医疗科技有限公司 | 纳米药物存储器、其制备方法及其应用 |
| KR102184768B1 (ko) * | 2018-12-31 | 2020-11-30 | 중앙대학교 산학협력단 | 혼합 고분자 미셀 조성물 및 이의 용도 |
Family Cites Families (16)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4419446A (en) * | 1980-12-31 | 1983-12-06 | The United States Of America As Represented By The Department Of Health And Human Services | Recombinant DNA process utilizing a papilloma virus DNA as a vector |
| FI77669C (fi) * | 1983-04-13 | 1989-04-10 | Ciba Geigy Ag | 20-spiroxaner och analoger, som innehaoller en oeppen ring e, foerfarande foer deras framstaellning samt dessa innehaollande farmaceutiska preparat. |
| US4588683A (en) * | 1984-02-06 | 1986-05-13 | Eastman Kodak Company | Method of preparing 11β, 17α, 20, 21-tetrahydroxy steroids and corresponding 11β, 17α, 21-trihydroxy-20-oxo steroids |
| US4935233A (en) * | 1985-12-02 | 1990-06-19 | G. D. Searle And Company | Covalently linked polypeptide cell modulators |
| US5869283A (en) * | 1988-05-06 | 1999-02-09 | Roussel Uclaf | Expression cassette operable in a recombinant host |
| AU642501B2 (en) * | 1990-04-30 | 1993-10-21 | Board Of Regents, The University Of Texas System | Steroid 5alpha-reductases |
| US5384253A (en) * | 1990-12-28 | 1995-01-24 | Dekalb Genetics Corporation | Genetic transformation of maize cells by electroporation of cells pretreated with pectin degrading enzymes |
| US5348886A (en) * | 1992-09-04 | 1994-09-20 | Monsanto Company | Method of producing recombinant eukaryotic viruses in bacteria |
| KR0180334B1 (ko) * | 1995-09-21 | 1999-03-20 | 김윤 | 블럭 공중합체 미셀을 이용한 약물전달체 및 이에 약물을 봉입하는 방법 |
| US5665428A (en) * | 1995-10-25 | 1997-09-09 | Macromed, Inc. | Preparation of peptide containing biodegradable microspheres by melt process |
| DK0900283T3 (da) * | 1995-12-12 | 2002-07-15 | Akzo Nobel Nv | Mikrobiel 11alfa-hydroxylering af steroider |
| KR100633939B1 (ko) * | 1997-10-03 | 2006-10-16 | 마크로메드 인코퍼레이티드 | 가역적 열 겔화 성질을 갖는 생분해성 저분자량 트리블럭폴리(락티드-코-글리콜리드) 폴리에틸렌 글리콜 공중합체 |
| US6201072B1 (en) * | 1997-10-03 | 2001-03-13 | Macromed, Inc. | Biodegradable low molecular weight triblock poly(lactide-co- glycolide) polyethylene glycol copolymers having reverse thermal gelation properties |
| NZ507835A (en) * | 1998-05-02 | 2003-01-31 | Astrazeneca Ab | Heterocyclic derivatives which inhibit factor XA |
| KR100274842B1 (ko) * | 1998-10-01 | 2001-03-02 | 김효근 | 미립구를 이용한 레티노익산의 서방형 약물방출 시스템 |
| US6338859B1 (en) * | 2000-06-29 | 2002-01-15 | Labopharm Inc. | Polymeric micelle compositions |
-
2001
- 2001-11-07 MX MXPA03004112A patent/MXPA03004112A/es unknown
- 2001-11-07 CA CA002428784A patent/CA2428784A1/fr not_active Abandoned
- 2001-11-07 ES ES01983010T patent/ES2289002T3/es not_active Expired - Lifetime
- 2001-11-07 AU AU2002214466A patent/AU2002214466A1/en not_active Abandoned
- 2001-11-07 AT AT01983010T patent/ATE369151T1/de not_active IP Right Cessation
- 2001-11-07 EP EP01983010A patent/EP1343530B1/fr not_active Expired - Lifetime
- 2001-11-07 CN CNB018186483A patent/CN100408099C/zh not_active Expired - Fee Related
- 2001-11-07 NZ NZ525726A patent/NZ525726A/en unknown
- 2001-11-07 US US10/415,677 patent/US20040076673A1/en not_active Abandoned
- 2001-11-07 KR KR10-2003-7006265A patent/KR20030057549A/ko not_active Application Discontinuation
- 2001-11-07 WO PCT/SE2001/002470 patent/WO2002038184A1/fr active IP Right Grant
- 2001-11-07 BR BR0115204-1A patent/BR0115204A/pt not_active IP Right Cessation
- 2001-11-07 DK DK01983010T patent/DK1343530T3/da active
- 2001-11-07 PT PT01983010T patent/PT1343530E/pt unknown
- 2001-11-07 IL IL15569101A patent/IL155691A0/xx unknown
- 2001-11-07 DE DE60129838T patent/DE60129838T2/de not_active Expired - Fee Related
- 2001-11-07 JP JP2002540766A patent/JP4255692B2/ja not_active Expired - Fee Related
-
2003
- 2003-05-08 NO NO20032070A patent/NO20032070L/no not_active Application Discontinuation
-
2004
- 2004-06-28 HK HK04104620.6A patent/HK1061646A1/xx not_active IP Right Cessation
-
2007
- 2007-10-05 CY CY20071101268T patent/CY1106908T1/el unknown
Also Published As
| Publication number | Publication date |
|---|---|
| DE60129838T2 (de) | 2008-04-30 |
| ES2289002T3 (es) | 2008-02-01 |
| KR20030057549A (ko) | 2003-07-04 |
| EP1343530B1 (fr) | 2007-08-08 |
| CA2428784A1 (fr) | 2002-05-16 |
| WO2002038184A1 (fr) | 2002-05-16 |
| NO20032070D0 (no) | 2003-05-08 |
| EP1343530A1 (fr) | 2003-09-17 |
| DK1343530T3 (da) | 2007-10-15 |
| JP4255692B2 (ja) | 2009-04-15 |
| PT1343530E (pt) | 2007-09-25 |
| JP2004513154A (ja) | 2004-04-30 |
| BR0115204A (pt) | 2004-02-03 |
| CN1474702A (zh) | 2004-02-11 |
| CY1106908T1 (el) | 2012-09-26 |
| IL155691A0 (en) | 2003-11-23 |
| DE60129838D1 (de) | 2007-09-20 |
| CN100408099C (zh) | 2008-08-06 |
| MXPA03004112A (es) | 2003-08-19 |
| NZ525726A (en) | 2004-10-29 |
| US20040076673A1 (en) | 2004-04-22 |
| NO20032070L (no) | 2003-07-07 |
| HK1061646A1 (en) | 2004-09-30 |
| ATE369151T1 (de) | 2007-08-15 |
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| MK4 | Application lapsed section 142(2)(d) - no continuation fee paid for the application |