JP2000026292A5 - - Google Patents

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Publication number
JP2000026292A5
JP2000026292A5 JP1998054124A JP5412498A JP2000026292A5 JP 2000026292 A5 JP2000026292 A5 JP 2000026292A5 JP 1998054124 A JP1998054124 A JP 1998054124A JP 5412498 A JP5412498 A JP 5412498A JP 2000026292 A5 JP2000026292 A5 JP 2000026292A5
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JP
Japan
Prior art keywords
pharmaceutical composition
oral pharmaceutical
release oral
composition according
active ingredient
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JP1998054124A
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Japanese (ja)
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JP2000026292A (en
JP4063386B2 (en
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Priority to JP05412498A priority Critical patent/JP4063386B2/en
Priority claimed from JP05412498A external-priority patent/JP4063386B2/en
Publication of JP2000026292A publication Critical patent/JP2000026292A/en
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Publication of JP4063386B2 publication Critical patent/JP4063386B2/en
Publication of JP2000026292A5 publication Critical patent/JP2000026292A5/ja
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Description

【特許請求の範囲】
【請求項1】 式
【化1】

Figure 2000026292
で表されるベンジルコハク酸誘導体のカルシウム塩またはその水和物を有効成分として含有する速放性経口医薬品組成物であって、二酸化ケイ素または部分アルファ化デンプンから選択される少なくとも1種を含有することを特徴とする、速放性経口医薬品組成物。
【請求項2】
【化2】
Figure 2000026292
で表されるベンジルコハク酸誘導体のカルシウム塩またはその水和物を有効成分として含有する速放性経口医薬品組成物であって、(a)乳糖、(b)トウモロコシデンプン、(c)結晶セルロース、および(d)二酸化ケイ素または部分アルファ化デンプンから選択される少なくとも1種を含有することを特徴とする、速放性経口医薬品組成物。
【請求項3】 二酸化ケイ素の含有量が、製剤全重量に対して0.5〜5重量%である、請求項1または2のいずれか一項記載の速放性経口医薬品組成物。
【請求項4】 部分アルファ化デンプンの含有量が、製剤全重量に対して5〜20重量%である、請求項1または2のいずれか一項記載の速放性経口医薬品組成物。
【請求項5】 剤形が、錠剤である、請求項1乃至4のいずれか一項記載の速放性経口医薬品組成物。
【請求項6】 服用後、有効成分が、20分以内に75%以上溶出されることを特徴とする、請求項1乃至5のいずれか一項記載の速放性経口医薬品組成物。
【請求項7】 日本薬局方溶出試験法第2法(パドル法)に従い、試験液として日本薬局方第1液を用い、50rpmとする溶出試験において、20分以内に75%以上溶出されることを特徴とする、請求項1乃至5のいずれか一項記載の速放性経口医薬品組成物。 [Claims]
    1. Expression
Embedded image
Figure 2000026292
-Release oral pharmaceutical composition containing, as an active ingredient, a calcium salt of a benzylsuccinic acid derivative represented by the formula:A rapid-release oral pharmaceutical composition comprising at least one selected from silicon dioxide and partially pregelatinized starch.
    (2) formula
Embedded image
Figure 2000026292
A rapid-release oral pharmaceutical composition containing, as an active ingredient, a calcium salt of a benzylsuccinic acid derivative represented by the formula (1), lactose, (b) corn starch, (c) crystalline cellulose, And (d) at least one selected from silicon dioxide or partially pregelatinized starch.
    (3) 3. The quick-release oral pharmaceutical composition according to claim 1, wherein the content of silicon dioxide is 0.5 to 5% by weight based on the total weight of the preparation.
    (4) The immediate release oral pharmaceutical composition according to any one of claims 1 to 2, wherein the content of the partially pregelatinized starch is 5 to 20% by weight based on the total weight of the preparation.
    (5) The immediate release oral pharmaceutical composition according to any one of claims 1 to 4, wherein the dosage form is a tablet.
    6. The quick-release oral pharmaceutical composition according to any one of claims 1 to 5, wherein 75% or more of the active ingredient is eluted within 20 minutes after administration.
    7. According to the Japanese Pharmacopoeia Dissolution Test Method 2 (paddle method), in a dissolution test at 50 rpm using Japanese Pharmacopoeia First Solution as a test solution, at least 75% is eluted within 20 minutes, An immediate release oral pharmaceutical composition according to any one of claims 1 to 5.

Figure 2000026292
Figure 2000026292

JP05412498A 1998-01-29 1998-01-29 Rapid-release oral pharmaceutical composition Expired - Fee Related JP4063386B2 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP05412498A JP4063386B2 (en) 1998-01-29 1998-01-29 Rapid-release oral pharmaceutical composition

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP05412498A JP4063386B2 (en) 1998-01-29 1998-01-29 Rapid-release oral pharmaceutical composition

Related Child Applications (1)

Application Number Title Priority Date Filing Date
JP2007271625A Division JP4072195B2 (en) 2007-10-18 2007-10-18 Immediate release oral pharmaceutical composition

Publications (3)

Publication Number Publication Date
JP2000026292A JP2000026292A (en) 2000-01-25
JP4063386B2 JP4063386B2 (en) 2008-03-19
JP2000026292A5 true JP2000026292A5 (en) 2009-01-08

Family

ID=12961859

Family Applications (1)

Application Number Title Priority Date Filing Date
JP05412498A Expired - Fee Related JP4063386B2 (en) 1998-01-29 1998-01-29 Rapid-release oral pharmaceutical composition

Country Status (1)

Country Link
JP (1) JP4063386B2 (en)

Families Citing this family (9)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP4568398B2 (en) * 2000-03-22 2010-10-27 キッセイ薬品工業株式会社 Hexahydroisoindoline acid addition salt and method of use thereof
JP2001261645A (en) * 2000-03-22 2001-09-26 Kissei Pharmaceut Co Ltd (3s)-3-methoxycarbonyl-4-phenylbutyryl chloride and method for using the same
EP1552830A4 (en) * 2002-06-28 2007-07-18 Kissei Pharmaceutical Drug composition for prevention or inhibition of advance of diabetic complication
US20050267195A1 (en) * 2002-06-28 2005-12-01 Imao Mikoshiba Drug composition for blood sugar control
JP4575654B2 (en) * 2003-09-05 2010-11-04 エスエス製薬株式会社 Pharmaceutical composition with improved solubility and fluidity
JP4733120B2 (en) * 2005-05-26 2011-07-27 大日本住友製薬株式会社 Pharmaceutical composition
JP5100634B2 (en) * 2006-03-24 2012-12-19 興和株式会社 Orally rapidly disintegrating tablets
CA2714524A1 (en) 2008-02-11 2009-08-20 Makiko Yanagida Tablet having improved elution properties
US20120040001A1 (en) 2009-02-12 2012-02-16 Fuji Chemical Industry Co., Ltd. Disintegrating particle composition and rapidly disintegrating compression-molded material used the same

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