JP5769626B2 - 溶媒および塩を用いるマイクロカプセル封入プロセス - Google Patents
溶媒および塩を用いるマイクロカプセル封入プロセス Download PDFInfo
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- JP5769626B2 JP5769626B2 JP2011527985A JP2011527985A JP5769626B2 JP 5769626 B2 JP5769626 B2 JP 5769626B2 JP 2011527985 A JP2011527985 A JP 2011527985A JP 2011527985 A JP2011527985 A JP 2011527985A JP 5769626 B2 JP5769626 B2 JP 5769626B2
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- 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
- A61K9/16—Agglomerates; Granulates; Microbeadlets ; Microspheres; Pellets; Solid products obtained by spray drying, spray freeze drying, spray congealing,(multiple) emulsion solvent evaporation or extraction
- A61K9/1682—Processes
- A61K9/1694—Processes resulting in granules or microspheres of the matrix type containing more than 5% of excipient
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/33—Heterocyclic compounds
- A61K31/335—Heterocyclic compounds having oxygen as the only ring hetero atom, e.g. fungichromin
- A61K31/365—Lactones
- A61K31/366—Lactones having six-membered rings, e.g. delta-lactones
- A61K31/37—Coumarins, e.g. psoralen
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- 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
-
- 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
- A61K9/16—Agglomerates; Granulates; Microbeadlets ; Microspheres; Pellets; Solid products obtained by spray drying, spray freeze drying, spray congealing,(multiple) emulsion solvent evaporation or extraction
- A61K9/1605—Excipients; Inactive ingredients
- A61K9/1629—Organic macromolecular compounds
- A61K9/1641—Organic macromolecular compounds obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds, e.g. polyethylene glycol, poloxamers
- A61K9/1647—Polyesters, e.g. poly(lactide-co-glycolide)
-
- 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
- A61K9/50—Microcapsules having a gas, liquid or semi-solid filling; Solid microparticles or pellets surrounded by a distinct coating layer, e.g. coated microspheres, coated drug crystals
- A61K9/5005—Wall or coating material
- A61K9/5021—Organic macromolecular compounds
- A61K9/5031—Organic macromolecular compounds obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds, e.g. polyethylene glycol, poly(lactide-co-glycolide)
-
- 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
- A61K9/50—Microcapsules having a gas, liquid or semi-solid filling; Solid microparticles or pellets surrounded by a distinct coating layer, e.g. coated microspheres, coated drug crystals
- A61K9/5089—Processes
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- Health & Medical Sciences (AREA)
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- Medicinal Chemistry (AREA)
- Pharmacology & Pharmacy (AREA)
- Epidemiology (AREA)
- Life Sciences & Earth Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- General Health & Medical Sciences (AREA)
- Public Health (AREA)
- Veterinary Medicine (AREA)
- Engineering & Computer Science (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Medicinal Preparation (AREA)
- Processes Of Treating Macromolecular Substances (AREA)
- Manufacturing Of Micro-Capsules (AREA)
- Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
Description
本出願は、米国特許仮出願第61/097,936号(2008年9月18日出願)および米国特許仮出願第61/146,856号(2009年1月23日出願)(これらの内容は各々、参照により本明細書中に組み込まれる)の利益を主張する。
定義
漸増塩濃度レベルでのPVA中の溶媒溶解度を測定するために、平衡/飽和試験を実施した。2%PVA水溶液中の塩化ナトリウム重量%を変更しながら、酢酸エチルおよび塩化メチレンの飽和溶解度(重量%)を個別に試験した。図1から分かるように、塩化ナトリウム含量が増大すると、2つの有機化合物の飽和溶解度は減少した。約15重量%塩化ナトリウム含量で、PVAは溶液の塩析を開始した。同様の傾向は、図2に示されるような1%PVA水溶液を用いて観察される。
実施例2
実施例3
実施例4
Claims (19)
- 微小粒子の製造のためのカプセル封入方法であって、以下の:
(a)連続プロセス媒体中に薬剤、ポリマーおよびポリマー用の第一溶媒を含む分散相を含むエマルションまたは二重エマルションを形成すること(ここで、前記連続プロセス媒体は、少なくとも1つの塩および少なくとも1つの第二溶媒を含み、前記第二溶媒は前記連続プロセス媒体中の前記第一溶媒の溶解度を低減する);ならびに
(b)前記第一溶媒を前記分散相から抽出して、前記微小粒子を形成すること、
を含み、
前記塩が、塩化ナトリウムまたは塩化カリウムである
方法。 - 前記第二溶媒が前記連続プロセス媒体中に飽和またはほぼ飽和量で存在する請求項1記載の方法。
- 前記塩が0.1〜20重量%の前記連続プロセス媒体中濃度で存在する請求項1または2に記載の方法。
- 前記第一および第二溶媒が同一溶媒である請求項1〜3のいずれかに記載の方法。
- 前記第一および第二溶媒が有機溶媒を含む請求項1〜4のいずれかに記載の方法。
- 前記第一および第二溶媒が塩化メチレンまたは酢酸エチルを含む請求項1〜5のいずれかに記載の方法。
- 前記第二溶媒が2つ以上の溶媒を含む請求項1〜6のいずれかに記載の方法。
- 前記連続プロセス媒体が水をさらに含む請求項1〜7のいずれかに記載の方法。
- 前記連続プロセス媒体が実質的に水をさらに含む請求項1〜8のいずれかに記載の方法。
- 前記連続プロセス媒体が界面活性剤をさらに含む請求項1〜9のいずれかに記載の方法。
- 前記界面活性剤がPVAを含む請求項10記載の方法。
- 前記分散相および連続プロセス媒体がエマルションを形成する請求項1〜11のいずれかに記載の方法。
- 前記分散相および連続プロセス媒体が二重エマルションを形成する請求項1〜12のいずれかに記載の方法。
- 前記連続プロセス媒体の温度が、前記連続プロセス媒体中の前記第一溶媒の溶解度を低減するために周囲温度から調整される請求項1〜13のいずれかに記載の方法。
- 前記連続プロセス媒体の温度が、前記連続プロセス媒体中の前記第一溶媒の溶解度を増大するために周囲温度から調整される請求項1〜14のいずれかに記載の方法。
- 前記結果的に生じる微小粒子の安息角が、連続プロセス媒体中に塩および/または溶媒を含まずに作製された結果生じる微小粒子の安息角より少なくとも10度小さい請求項1〜15のいずれかに記載の方法。
- 前記結果的に生じる微小粒子の安息角が、連続プロセス媒体中に塩および/または溶媒を含まずに作製された結果生じる微小粒子の安息角より少なくとも15度小さい請求項1〜16のいずれかに記載の方法。
- 前記結果的に生じる微小粒子の安息角が、連続プロセス媒体中に塩および/または溶媒を含まずに作製された結果生じる微小粒子の安息角より少なくとも20度小さい請求項1〜17のいずれかに記載の方法。
- 薬剤、ポリマーおよびポリマーのための第一溶媒を含む分散相、ならびに水、第二溶媒(ここで、前記第二溶媒は水中の第一溶媒の溶解度を低減する)、および前記水中の前記第一溶媒の溶解度を低減する塩を含む連続相を含むエマルションであって、
前記塩が、塩化ナトリウムまたは塩化カリウムであるエマルション。
Applications Claiming Priority (5)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US9793608P | 2008-09-18 | 2008-09-18 | |
US61/097,936 | 2008-09-18 | ||
US14685609P | 2009-01-23 | 2009-01-23 | |
US61/146,856 | 2009-01-23 | ||
PCT/US2009/057437 WO2010033776A1 (en) | 2008-09-18 | 2009-09-18 | Microencapsulation process with solvent and salt |
Related Child Applications (1)
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JP2015062015A Division JP6124935B2 (ja) | 2008-09-18 | 2015-03-25 | 溶媒および塩を用いるマイクロカプセル封入プロセス |
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JP2012503084A JP2012503084A (ja) | 2012-02-02 |
JP5769626B2 true JP5769626B2 (ja) | 2015-08-26 |
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JP2011527985A Active JP5769626B2 (ja) | 2008-09-18 | 2009-09-18 | 溶媒および塩を用いるマイクロカプセル封入プロセス |
JP2015062015A Active JP6124935B2 (ja) | 2008-09-18 | 2015-03-25 | 溶媒および塩を用いるマイクロカプセル封入プロセス |
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Country Status (6)
Country | Link |
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US (1) | US10821080B2 (ja) |
EP (1) | EP2334288B1 (ja) |
JP (2) | JP5769626B2 (ja) |
CA (1) | CA2737484C (ja) |
ES (1) | ES2877206T3 (ja) |
WO (1) | WO2010033776A1 (ja) |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
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JP2015134810A (ja) * | 2008-09-18 | 2015-07-27 | エボニック コーポレイションEvonik Corporation | 溶媒および塩を用いるマイクロカプセル封入プロセス |
Families Citing this family (11)
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US10092524B2 (en) | 2008-06-11 | 2018-10-09 | Edge Therapeutics, Inc. | Compositions and their use to treat complications of aneurysmal subarachnoid hemorrhage |
KR20120011344A (ko) * | 2010-07-21 | 2012-02-08 | 에스케이케미칼주식회사 | 고분자 미립구의 제조방법 및 그 방법에 의해 제조된 고분자 미립구 |
RU2606169C2 (ru) | 2011-04-05 | 2017-01-10 | Эдж Терапьютикс | Система интравентрикулярной доставки лекарственного средства для улучшения исхода после повреждения головного мозга, нарушающего мозговое кровообращение |
US9399019B2 (en) | 2012-05-09 | 2016-07-26 | Evonik Corporation | Polymorph compositions, methods of making, and uses thereof |
CN109069416A (zh) | 2016-02-23 | 2018-12-21 | 拜欧帝力威瑞科学有限公司 | 缓释丁丙诺啡微球(srbm)及其使用方法 |
US10329528B2 (en) * | 2016-04-06 | 2019-06-25 | The Curators Of The University Of Missouri | Method of forming microparticles for use in cell seeding |
WO2018022554A1 (en) * | 2016-07-26 | 2018-02-01 | Board Of Regents, The University Of Texas System | Microparticle carriers for aqueous compositions and methods of making |
CN106996857B (zh) * | 2017-03-22 | 2019-05-10 | 大连理工大学 | 一种赫尔肖盒子及其构成的对流混合实验*** |
KR102645701B1 (ko) * | 2017-09-03 | 2024-03-12 | 에보니크 오퍼레이션즈 게엠베하 | 적층 가공을 위한 생체적합성 중합체 분말 |
CA3077011A1 (en) * | 2017-09-26 | 2019-04-04 | Nanomi B.V. | Method for preparing micro-particles by double emulsion technique |
JP2023514874A (ja) * | 2019-10-31 | 2023-04-11 | エボニック オペレーションズ ゲーエムベーハー | キャリアポリマーおよび1つ以上の生物学的に活性な成分を含むナノ粒子またはマイクロ粒子を製造する方法 |
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FR2839260B1 (fr) * | 2002-05-03 | 2005-02-25 | Inst Nat Sante Rech Med | Microparticules a base d'un materiau bicompatible et biodegradable, supportant des cellules et des substances biologiquement actives |
US20050129776A1 (en) * | 2002-05-03 | 2005-06-16 | Inserm | Microparticles supporting cells and active substances |
US20040097419A1 (en) * | 2002-11-19 | 2004-05-20 | Holger Petersen | Organic compounds |
US7083748B2 (en) * | 2003-02-07 | 2006-08-01 | Ferro Corporation | Method and apparatus for continuous particle production using supercritical fluid |
FR2867075B1 (fr) * | 2004-03-03 | 2006-07-14 | Ethypharm Sa | Procede de preparation de microspheres biodegradables calibrees |
WO2005122734A2 (en) * | 2004-06-14 | 2005-12-29 | The Research Foundation Of State University Of New York | Nanosphere/microsphere delivery system for the treatment of spinal cord injury |
CA2578694C (en) * | 2004-09-01 | 2014-02-25 | Appleton Papers Inc. | Encapsulated cure systems |
DE102008012908A1 (de) | 2008-03-06 | 2009-09-10 | Boehringer Ingelheim Pharma Gmbh & Co. Kg | Methode zum anti-inflammatorischen und anti-ödematösen Schutz von explantiertem biologischen Material bis zu seiner Transplantation in Patienten |
WO2010033776A1 (en) * | 2008-09-18 | 2010-03-25 | Surmodics Pharmaceuticals, Inc. | Microencapsulation process with solvent and salt |
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2009
- 2009-09-18 WO PCT/US2009/057437 patent/WO2010033776A1/en active Application Filing
- 2009-09-18 JP JP2011527985A patent/JP5769626B2/ja active Active
- 2009-09-18 US US12/562,455 patent/US10821080B2/en active Active
- 2009-09-18 ES ES09792697T patent/ES2877206T3/es active Active
- 2009-09-18 EP EP09792697.6A patent/EP2334288B1/en active Active
- 2009-09-18 CA CA2737484A patent/CA2737484C/en active Active
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Cited By (1)
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JP2015134810A (ja) * | 2008-09-18 | 2015-07-27 | エボニック コーポレイションEvonik Corporation | 溶媒および塩を用いるマイクロカプセル封入プロセス |
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JP2015134810A (ja) | 2015-07-27 |
EP2334288B1 (en) | 2021-05-19 |
EP2334288A1 (en) | 2011-06-22 |
CA2737484A1 (en) | 2010-03-25 |
JP6124935B2 (ja) | 2017-05-10 |
JP2012503084A (ja) | 2012-02-02 |
ES2877206T3 (es) | 2021-11-16 |
US10821080B2 (en) | 2020-11-03 |
WO2010033776A1 (en) | 2010-03-25 |
CA2737484C (en) | 2017-10-10 |
US20100069602A1 (en) | 2010-03-18 |
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