KR900004325A - 유핵 과립 및 그의 제조방법 - Google Patents

유핵 과립 및 그의 제조방법 Download PDF

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Publication number
KR900004325A
KR900004325A KR1019890013906A KR890013906A KR900004325A KR 900004325 A KR900004325 A KR 900004325A KR 1019890013906 A KR1019890013906 A KR 1019890013906A KR 890013906 A KR890013906 A KR 890013906A KR 900004325 A KR900004325 A KR 900004325A
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KR
South Korea
Prior art keywords
granules
dispersion
core
active ingredient
spraying
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KR1019890013906A
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English (en)
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KR0143424B1 (ko
Inventor
히로요시 고야마
순이찌 이또오
신이찌로 히라이
Original Assignee
우메모또 요시마사
다께다야꾸힝고오교 가부시끼가이샤
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Publication of KR900004325A publication Critical patent/KR900004325A/ko
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Publication of KR0143424B1 publication Critical patent/KR0143424B1/ko

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    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K9/00Medicinal preparations characterised by special physical form
    • A61K9/14Particulate form, e.g. powders, Processes for size reducing of pure drugs or the resulting products, Pure drug nanoparticles
    • A61K9/16Agglomerates; Granulates; Microbeadlets ; Microspheres; Pellets; Solid products obtained by spray drying, spray freeze drying, spray congealing,(multiple) emulsion solvent evaporation or extraction
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K9/00Medicinal preparations characterised by special physical form
    • A61K9/48Preparations in capsules, e.g. of gelatin, of chocolate
    • A61K9/50Microcapsules 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
    • A61K9/5073Microcapsules 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 having two or more different coatings optionally including drug-containing subcoatings
    • A61K9/5078Microcapsules 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 having two or more different coatings optionally including drug-containing subcoatings with drug-free core
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K47/00Medicinal preparations characterised by the non-active ingredients used, e.g. carriers or inert additives; Targeting or modifying agents chemically bound to the active ingredient
    • A61K47/30Macromolecular organic or inorganic compounds, e.g. inorganic polyphosphates
    • A61K47/36Polysaccharides; Derivatives thereof, e.g. gums, starch, alginate, dextrin, hyaluronic acid, chitosan, inulin, agar or pectin
    • A61K47/38Cellulose; Derivatives thereof
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K9/00Medicinal preparations characterised by special physical form
    • A61K9/14Particulate form, e.g. powders, Processes for size reducing of pure drugs or the resulting products, Pure drug nanoparticles
    • A61K9/16Agglomerates; Granulates; Microbeadlets ; Microspheres; Pellets; Solid products obtained by spray drying, spray freeze drying, spray congealing,(multiple) emulsion solvent evaporation or extraction
    • A61K9/167Agglomerates; Granulates; Microbeadlets ; Microspheres; Pellets; Solid products obtained by spray drying, spray freeze drying, spray congealing,(multiple) emulsion solvent evaporation or extraction with an outer layer or coating comprising drug; with chemically bound drugs or non-active substances on their surface
    • A61K9/1676Agglomerates; Granulates; Microbeadlets ; Microspheres; Pellets; Solid products obtained by spray drying, spray freeze drying, spray congealing,(multiple) emulsion solvent evaporation or extraction with an outer layer or coating comprising drug; with chemically bound drugs or non-active substances on their surface having a drug-free core with discrete complete coating layer containing drug
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K9/00Medicinal preparations characterised by special physical form
    • A61K9/20Pills, tablets, discs, rods
    • A61K9/2072Pills, tablets, discs, rods characterised by shape, structure or size; Tablets with holes, special break lines or identification marks; Partially coated tablets; Disintegrating flat shaped forms
    • A61K9/2077Tablets comprising drug-containing microparticles in a substantial amount of supporting matrix; Multiparticulate tablets
    • A61K9/2081Tablets comprising drug-containing microparticles in a substantial amount of supporting matrix; Multiparticulate tablets with microcapsules or coated microparticles according to A61K9/50

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  • Health & Medical Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Chemical & Material Sciences (AREA)
  • Animal Behavior & Ethology (AREA)
  • Veterinary Medicine (AREA)
  • Epidemiology (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Medicinal Chemistry (AREA)
  • General Health & Medical Sciences (AREA)
  • Public Health (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Inorganic Chemistry (AREA)
  • Medicinal Preparation (AREA)
  • Saccharide Compounds (AREA)
  • Agricultural Chemicals And Associated Chemicals (AREA)
  • Cosmetics (AREA)
  • Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)

Abstract

내용 없음

Description

유핵 과립 및 그의 제조방법
본 내용은 요부공개 건이므로 전문내용을 수록하지 않았음

Claims (7)

  1. 중심과립들에 저치환 히드록시프로필셀룰로오스의 분산액을 분무하는 것을 포함함을 특징으로 하는 유핵 과립의 제조방법.
  2. 제1항에 있어서, 저치완 히드록시프로필셀룰로오스가 약 4∼20%, 바람직하게는, 5∼16%, 보다 바람직하게는 10∼13%의 비율로 히드록시프로폭실기를 함유함을 특징으로 하는 방법.
  3. 제1항에 있어서, 과립에 분산액을 분무하는 동안 분말형태의 살포제를 살포함을 특징으로 하는 방법.
  4. 제1항에 있어서, 분산액에 활성 성분을 첨가 배합함을 특징으로 하는 방법.
  5. 제3항에 있어서, 분말형태의 살포제에 활성 성분을 첨가 배합함을 특징으로 하는 방법.
  6. 제4항 또는 제5항에 있어서, 활성 성분이 약물임을 특징으로 하는 방법.
  7. 제1항 내지 제6항중 어느 한항에서 청구한 방법에 의해 수득되는 유핵 과립.
    ※ 참고사항 : 최초출원 내용에 의하여 공개하는 것임.
KR1019890013906A 1988-09-27 1989-09-27 유핵 과립 및 그의 제조방법 KR0143424B1 (ko)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
JP24354388 1988-09-27
JP63-243543 1988-09-27
JP243543/1988 1988-09-27

Publications (2)

Publication Number Publication Date
KR900004325A true KR900004325A (ko) 1990-04-12
KR0143424B1 KR0143424B1 (ko) 1998-07-15

Family

ID=17105442

Family Applications (1)

Application Number Title Priority Date Filing Date
KR1019890013906A KR0143424B1 (ko) 1988-09-27 1989-09-27 유핵 과립 및 그의 제조방법

Country Status (11)

Country Link
US (1) US5855914A (ko)
EP (1) EP0361874B1 (ko)
KR (1) KR0143424B1 (ko)
AT (1) ATE97317T1 (ko)
AU (1) AU626584B2 (ko)
CA (1) CA1338596C (ko)
DE (1) DE68910773T2 (ko)
DK (1) DK473889A (ko)
ES (1) ES2060784T3 (ko)
IE (1) IE63039B1 (ko)
NZ (1) NZ230763A (ko)

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DE59710349D1 (de) * 1996-04-04 2003-07-31 Felix Specht Verfahren zur herstellung von gering dosierten freifliessenden und/oder direktkomprimierbaren pulversystemen
TW580397B (en) * 1997-05-27 2004-03-21 Takeda Chemical Industries Ltd Solid preparation
FR2771291B1 (fr) * 1997-11-21 2000-02-25 Ethypharm Lab Prod Ethiques Spheroides, procede de preparation et compositions pharmaceutiques
FR2771292B1 (fr) * 1997-11-21 2000-02-18 Ethypharm Lab Prod Ethiques Spheroides contenant de la tiagabine, procede de preparation et compositions pharmaceutiques
US6328994B1 (en) 1998-05-18 2001-12-11 Takeda Chemical Industries, Ltd. Orally disintegrable tablets
EP1561458B1 (en) * 1998-07-28 2010-09-15 Takeda Pharmaceutical Company Limited Rapidly disintegrable solid preparation
US6555139B2 (en) 1999-06-28 2003-04-29 Wockhardt Europe Limited Preparation of micron-size pharmaceutical particles by microfluidization
US6245913B1 (en) 1999-06-30 2001-06-12 Wockhardt Europe Limited Synthetic procedure for 5-methoxy-2-[(4-methoxy-3,5-dimethyl-2-pyridinyl)-methylthio]-IH-benzimidazole hydrochloride and its conversion to omeprazole
CA2313504C (en) 1999-07-12 2007-05-29 Douglas P. Debernardi Folic acid in solid dosage forms
FR2796840B1 (fr) * 1999-07-26 2003-06-20 Ethypharm Lab Prod Ethiques Comprimes faiblement doses et procede de preparation
EP1238662B1 (en) * 2001-03-07 2006-05-31 Dainippon Sumitomo Pharma Co., Ltd. Method for manufacturing drug granules, the drug granules and pharmaceutical preparation containing the drug granules
US20070059368A1 (en) * 2005-05-31 2007-03-15 Cherukuri S R Modified release formulations of anti-irritability drugs
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Also Published As

Publication number Publication date
DE68910773T2 (de) 1994-05-11
EP0361874A3 (en) 1991-01-30
IE63039B1 (en) 1995-03-22
US5855914A (en) 1999-01-05
DE68910773D1 (de) 1993-12-23
AU626584B2 (en) 1992-08-06
AU4233289A (en) 1990-04-05
KR0143424B1 (ko) 1998-07-15
EP0361874A2 (en) 1990-04-04
ATE97317T1 (de) 1993-12-15
IE893075L (en) 1990-03-27
ES2060784T3 (es) 1994-12-01
EP0361874B1 (en) 1993-11-18
CA1338596C (en) 1996-09-17
DK473889D0 (da) 1989-09-26
NZ230763A (en) 1991-10-25
DK473889A (da) 1990-03-28

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