KR880004806A - 분무 건조 아세트아미노펜 - Google Patents
분무 건조 아세트아미노펜 Download PDFInfo
- Publication number
- KR880004806A KR880004806A KR870011625A KR870011625A KR880004806A KR 880004806 A KR880004806 A KR 880004806A KR 870011625 A KR870011625 A KR 870011625A KR 870011625 A KR870011625 A KR 870011625A KR 880004806 A KR880004806 A KR 880004806A
- Authority
- KR
- South Korea
- Prior art keywords
- acetaminophen
- weight
- powder
- plasticizer
- water
- Prior art date
Links
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
- A61K9/0087—Galenical forms not covered by A61K9/02 - A61K9/7023
- A61K9/0095—Drinks; Beverages; Syrups; Compositions for reconstitution thereof, e.g. powders or tablets to be dispersed in a glass of water; Veterinary drenches
-
- 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
- A61K31/16—Amides, e.g. hydroxamic acids
- A61K31/165—Amides, e.g. hydroxamic acids having aromatic rings, e.g. colchicine, atenolol, progabide
-
- 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
- A61K9/0012—Galenical forms characterised by the site of application
- A61K9/0053—Mouth and digestive tract, i.e. intraoral and peroral administration
- A61K9/0056—Mouth soluble or dispersible forms; Suckable, eatable, chewable coherent forms; Forms rapidly disintegrating in the mouth; Lozenges; Lollipops; Bite capsules; Baked products; Baits or other oral forms for animals
-
- 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
-
- 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
- A61K9/1617—Organic compounds, e.g. phospholipids, fats
-
- 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
- A61K9/1652—Polysaccharides, e.g. alginate, cellulose derivatives; Cyclodextrin
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P25/00—Drugs for disorders of the nervous system
- A61P25/04—Centrally acting analgesics, e.g. opioids
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P29/00—Non-central analgesic, antipyretic or antiinflammatory agents, e.g. antirheumatic agents; Non-steroidal antiinflammatory drugs [NSAID]
Landscapes
- Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Veterinary Medicine (AREA)
- Chemical & Material Sciences (AREA)
- General Health & Medical Sciences (AREA)
- Public Health (AREA)
- Animal Behavior & Ethology (AREA)
- Pharmacology & Pharmacy (AREA)
- Medicinal Chemistry (AREA)
- Epidemiology (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Engineering & Computer Science (AREA)
- Nutrition Science (AREA)
- Physiology (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Organic Chemistry (AREA)
- General Chemical & Material Sciences (AREA)
- Zoology (AREA)
- Pain & Pain Management (AREA)
- Molecular Biology (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Biophysics (AREA)
- Rheumatology (AREA)
- Neurology (AREA)
- Biomedical Technology (AREA)
- Neurosurgery (AREA)
- Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
- Medicinal Preparation (AREA)
- Processes Of Treating Macromolecular Substances (AREA)
- Glanulating (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
Abstract
내용 없음
Description
본 내용은 요부공개 건이므로 전문내용을 수록하지 않았음
Claims (7)
- 필수적으로, 분말의 중량을 기준하여, 아세트 아미노펜 약 63 내지 77중량%, 에틸 셀룰로즈 약 15 내지 30중량% 및 가소제 약 2 내지 7중량%로 이루어지며, 용해되거나 현탁된 가소제를 함유하는 물 중의 아세트 아미노펜 및 에틸 셀룰로즈의 분산액으로부터 분무 건조된 분무 건조 아세트아미노펜의 치료학적 분말.
- 제1항에 있어서, 가소제가 디부틸 세바케이트, 글리세린, 프로필렌 글리콜, 트리아세틴 또는 폴리에틸렌 글리콜인 분말.
- 용해되거나 현탁된 가소제를 함유하는 물중의 아세트아미노펜 및 에틸 셀룰로즈의 분산액을 분무 건조 시킴을 특징으로 하여, 필수적으로, 분말의 중량을 기준하여, 아세트아미노펜 약 63 내지 77중량%, 에틸 셀룰로즈 약 15 내지 30중량% 및 가소제 약 2 내지 7중량%로 이루어진 분무 건조 아세트아미노펜의 치료학적 분말을 제조하는 방법.
- 제3항에 있어서, 가소제가 디부틸 세바케이트, 글리세린, 프로필렌 글리콜, 트리아세틴 또는 폴리에틸렌 글리콜인 방법.
- 제1항 또는 2항에 청구된 치료학적 분말을 함유함을 특징으로 하는, 물에 의해 10초 이내에 붕해 될 수 있는 경구 투여용 약제학적 고체 용량 형태.
- 고체 용량 형태가 물에 의해 10초 이내에 붕해될 수 있도록, 단위 용량의 약제학적 물질을 담지(carring)하는, 약제학적 물질에 대해 불활성인 약제학적으로 허용되는 수용성 또는 수분산성 담체물질의 네트워크(이 네트워크는 약제학적 물질 및 용매 중의 담체물질의 용액을 함유하는 조성물로 부터 용매를 승화시킴으로써 고체 상태로 수득된다)를 함유하는 고체용량형태에 있어서, 약제학적 물질이 제1항 또는 2항에 청구된 치료학적 분말임을 특징으로 하는 경구투여용 약제학적 고체 용량 형태.
- 제1항 또는 2항에 청구된 분말을 함유하는 씹을 수 있는 정제.※ 참고사항 : 최초출원 내용에 의하여 공개하는 것임.
Applications Claiming Priority (3)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US921,658 | 1978-07-03 | ||
US921658 | 1986-10-21 | ||
US06/921,658 US4760094A (en) | 1986-10-21 | 1986-10-21 | Spray dried acetaminophen |
Publications (2)
Publication Number | Publication Date |
---|---|
KR880004806A true KR880004806A (ko) | 1988-06-27 |
KR950013753B1 KR950013753B1 (ko) | 1995-11-15 |
Family
ID=25445764
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
KR1019870011625A KR950013753B1 (ko) | 1986-10-21 | 1987-10-20 | 분무 건조된 아세트아미노펜, 이의 제조방법 및 이를 함유하는 약제학적 제형 |
Country Status (11)
Country | Link |
---|---|
US (1) | US4760094A (ko) |
EP (1) | EP0267702B1 (ko) |
JP (1) | JP2550362B2 (ko) |
KR (1) | KR950013753B1 (ko) |
AT (1) | ATE83923T1 (ko) |
AU (1) | AU588136B2 (ko) |
CA (1) | CA1291044C (ko) |
DE (1) | DE3783332T2 (ko) |
ES (1) | ES2052578T3 (ko) |
GR (1) | GR3006761T3 (ko) |
IE (1) | IE61951B1 (ko) |
Families Citing this family (37)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US4946684A (en) * | 1989-06-20 | 1990-08-07 | American Home Products Corporation | Fast dissolving dosage forms |
US5198228A (en) * | 1989-09-14 | 1993-03-30 | Hoechst-Roussel Pharmaceuticals Inc. | Direct dry compressible acetaminophen tablet |
US5037658A (en) * | 1989-09-14 | 1991-08-06 | Hoechst-Roussel Pharmaceuticals, Inc. | Direct dry compressible acetaminophen composition |
US5130140A (en) * | 1989-09-14 | 1992-07-14 | Hoeschst-Roussel Pharmaceuticals Inc. | Method of making direct dry compressible acetaminophen composition |
US5358717A (en) * | 1989-12-22 | 1994-10-25 | Syntex (U.S.A.) Inc. | Directly-compressible naproxen or naproxen sodium compositions |
EP0580860B2 (en) * | 1991-04-16 | 2004-12-15 | Nippon Shinyaku Company, Limited | Method of manufacturing solid dispersion |
EP0620728B1 (en) * | 1992-01-13 | 1997-01-08 | Pfizer Inc. | Preparation of tablets of increased strength |
IL109460A (en) | 1993-05-10 | 1998-03-10 | Euro Celtique Sa | Controlled release formulation comprising tramadol |
IL110014A (en) | 1993-07-01 | 1999-11-30 | Euro Celtique Sa | Solid controlled-release oral dosage forms of opioid analgesics |
US7740881B1 (en) | 1993-07-01 | 2010-06-22 | Purdue Pharma Lp | Method of treating humans with opioid formulations having extended controlled release |
US5879705A (en) * | 1993-07-27 | 1999-03-09 | Euro-Celtique S.A. | Sustained release compositions of morphine and a method of preparing pharmaceutical compositions |
KR100354702B1 (ko) * | 1993-11-23 | 2002-12-28 | 유로-셀티크 소시에떼 아노뉨 | 약학조성물의제조방법및서방형조성물 |
US5891471A (en) * | 1993-11-23 | 1999-04-06 | Euro-Celtique, S.A. | Pharmaceutical multiparticulates |
US5843480A (en) * | 1994-03-14 | 1998-12-01 | Euro-Celtique, S.A. | Controlled release diamorphine formulation |
GB9422154D0 (en) | 1994-11-03 | 1994-12-21 | Euro Celtique Sa | Pharmaceutical compositions and method of producing the same |
US5965161A (en) | 1994-11-04 | 1999-10-12 | Euro-Celtique, S.A. | Extruded multi-particulates |
AU751497B2 (en) * | 1996-04-23 | 2002-08-15 | Mayne Pharma International Pty Ltd | Taste masked pharmaceutical compositions |
AUPN940796A0 (en) * | 1996-04-23 | 1996-05-16 | F.H. Faulding & Co. Limited | Taste masked pharmaceutical compositions |
AUPO637197A0 (en) * | 1997-04-23 | 1997-05-15 | F.H. Faulding & Co. Limited | Taste-masked pharmaceutical compositions |
FR2766089B1 (fr) * | 1997-07-21 | 2000-06-02 | Prographarm Lab | Comprime multiparticulaire perfectionne a delitement rapide |
US6270790B1 (en) | 1998-08-18 | 2001-08-07 | Mxneil-Ppc, Inc. | Soft, convex shaped chewable tablets having reduced friability |
US6806294B2 (en) | 1998-10-15 | 2004-10-19 | Euro-Celtique S.A. | Opioid analgesic |
DE19918325A1 (de) | 1999-04-22 | 2000-10-26 | Euro Celtique Sa | Verfahren zur Herstellung von Arzneiformen mit regulierter Wirkstofffreisetzung mittels Extrusion |
US6437000B1 (en) | 1999-09-02 | 2002-08-20 | Norstrum Pharmaceuticals, Inc. | Controlled release oral dosage for suitable for oral administration |
US10179130B2 (en) | 1999-10-29 | 2019-01-15 | Purdue Pharma L.P. | Controlled release hydrocodone formulations |
CA2389235C (en) | 1999-10-29 | 2007-07-17 | Euro-Celtique, S.A. | Controlled release hydrocodone formulations |
EP1295595A4 (en) * | 2000-06-30 | 2008-04-02 | Astellas Pharma Inc | TABLET RAPIDLY DISINTEGRATING IN THE MOUTH AND CORRESPONDING PRODUCTION PROCESS |
US6656492B2 (en) | 2000-06-30 | 2003-12-02 | Yamanouchi Pharmaceutical Co., Ltd. | Quick disintegrating tablet in buccal cavity and manufacturing method thereof |
EP2283829A1 (en) | 2000-10-30 | 2011-02-16 | Euro-Celtique S.A. | Controlled release hydrocodone formulations |
US20110104214A1 (en) | 2004-04-15 | 2011-05-05 | Purdue Pharma L.P. | Once-a-day oxycodone formulations |
UA81224C2 (uk) | 2001-05-02 | 2007-12-25 | Euro Celtic S A | Дозована форма оксикодону та її застосування |
US7972621B2 (en) * | 2004-06-03 | 2011-07-05 | R.P. Scherer Technologies, Llc | Process for formulating fast dispersing dosage forms comprising at least one fish gelatin selected on the basis of molecular weight |
US9925138B2 (en) | 2015-01-20 | 2018-03-27 | Handa Pharmaceuticals, Llc | Stable solid fingolimod dosage forms |
FI3562486T3 (fi) | 2016-12-31 | 2024-06-04 | Bioxcel Therapeutics Inc | Kielenalaisen deksmedetomidiinin käyttö agitaation hoidossa |
KR20210028192A (ko) | 2018-06-27 | 2021-03-11 | 바이오엑셀 테라퓨틱스 인코포레이티드 | 덱스메데토미딘을 함유하는 필름 제형 및 이를 생산하는 방법 |
JP2022540706A (ja) | 2019-07-19 | 2022-09-16 | バイオエクセル セラピューティクス,インコーポレイテッド | 鎮静作用のないデクスメデトミジン治療レジメン |
US11806334B1 (en) | 2023-01-12 | 2023-11-07 | Bioxcel Therapeutics, Inc. | Non-sedating dexmedetomidine treatment regimens |
Family Cites Families (11)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS5420572B2 (ko) * | 1973-04-27 | 1979-07-24 | ||
IE45770B1 (en) * | 1976-10-06 | 1982-11-17 | Wyeth John & Brother Ltd | Pharmaceutical dosage forms |
ATE17650T1 (de) * | 1980-05-20 | 1986-02-15 | Mallinckrodt Inc | Trockenpulverisierte n-acetyl-p-aminophenolzusammensetzungenund verfahren zu deren herstellung. |
US4439453A (en) * | 1980-12-22 | 1984-03-27 | Monsanto Company | Directly compressible acetaminophen granulation |
JPS58172311A (ja) * | 1982-04-02 | 1983-10-11 | Kodama Kk | 持続性製剤及びその製法 |
DE3306012A1 (de) * | 1983-02-22 | 1984-08-23 | Hoechst Ag, 6230 Frankfurt | Verfahren zur herstellung eines freifliessenden paracetamol-granulats |
US4600579A (en) * | 1983-06-07 | 1986-07-15 | Mallinckrodt, Inc. | N-acetyl-p-aminophenol compositions containing partially gelatinized starch and method for preparing same |
US4533674A (en) * | 1983-10-24 | 1985-08-06 | Basf Wyandotte Corporation | Process for preparing a sugar and starch free spray-dried vitamin C powder containing 90 percent ascorbic acid |
AU3880185A (en) * | 1984-02-08 | 1985-08-27 | R.P. Scherer Corporation | Acetaminophen gelatin capsule |
US4631284A (en) * | 1984-11-19 | 1986-12-23 | Mallinckrodt, Inc. | Acetaminophen compositions containing low doses of chlorpheniramine maleate, method for preparing same and tablets formed therefrom |
US4710519A (en) * | 1985-09-30 | 1987-12-01 | Basf Corporation | Process for preparing spray dried acetaminophen powder and the powder prepared thereby |
-
1986
- 1986-10-21 US US06/921,658 patent/US4760094A/en not_active Expired - Lifetime
-
1987
- 1987-10-09 AU AU79507/87A patent/AU588136B2/en not_active Ceased
- 1987-10-09 CA CA000548997A patent/CA1291044C/en not_active Expired - Fee Related
- 1987-10-13 IE IE275087A patent/IE61951B1/en not_active IP Right Cessation
- 1987-10-20 AT AT87309254T patent/ATE83923T1/de not_active IP Right Cessation
- 1987-10-20 KR KR1019870011625A patent/KR950013753B1/ko not_active IP Right Cessation
- 1987-10-20 EP EP87309254A patent/EP0267702B1/en not_active Expired - Lifetime
- 1987-10-20 JP JP62266139A patent/JP2550362B2/ja not_active Expired - Lifetime
- 1987-10-20 DE DE8787309254T patent/DE3783332T2/de not_active Expired - Fee Related
- 1987-10-20 ES ES87309254T patent/ES2052578T3/es not_active Expired - Lifetime
-
1993
- 1993-01-11 GR GR930400017T patent/GR3006761T3/el unknown
Also Published As
Publication number | Publication date |
---|---|
EP0267702B1 (en) | 1992-12-30 |
CA1291044C (en) | 1991-10-22 |
IE872750L (en) | 1988-04-21 |
EP0267702A3 (en) | 1989-06-14 |
ES2052578T3 (es) | 1994-07-16 |
DE3783332T2 (de) | 1993-05-27 |
DE3783332D1 (de) | 1993-02-11 |
EP0267702A2 (en) | 1988-05-18 |
US4760094A (en) | 1988-07-26 |
AU7950787A (en) | 1988-04-28 |
ATE83923T1 (de) | 1993-01-15 |
AU588136B2 (en) | 1989-09-07 |
GR3006761T3 (ko) | 1993-06-30 |
KR950013753B1 (ko) | 1995-11-15 |
IE61951B1 (en) | 1994-11-30 |
JP2550362B2 (ja) | 1996-11-06 |
JPS63112514A (ja) | 1988-05-17 |
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