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
- Authority
- JP
- Japan
- Prior art keywords
- pharmaceutical composition
- oral pharmaceutical
- release oral
- composition according
- active ingredient
- 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.)
- Granted
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- 239000008203 oral pharmaceutical composition Substances 0.000 description 8
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 6
- 229920000881 Modified starch Polymers 0.000 description 3
- 239000004480 active ingredient Substances 0.000 description 3
- 239000000377 silicon dioxide Substances 0.000 description 3
- 235000012239 silicon dioxide Nutrition 0.000 description 3
- GTOFKXZQQDSVFH-UHFFFAOYSA-N 2-benzylsuccinic acid Chemical class OC(=O)CC(C(O)=O)CC1=CC=CC=C1 GTOFKXZQQDSVFH-UHFFFAOYSA-N 0.000 description 2
- 159000000007 calcium salts Chemical class 0.000 description 2
- 238000007922 dissolution test Methods 0.000 description 2
- 238000002360 preparation method Methods 0.000 description 2
- 229920002261 Corn starch Polymers 0.000 description 1
- GUBGYTABKSRVRQ-UUNJERMWSA-N Lactose Natural products O([C@@H]1[C@H](O)[C@H](O)[C@H](O)O[C@@H]1CO)[C@H]1[C@@H](O)[C@@H](O)[C@H](O)[C@H](CO)O1 GUBGYTABKSRVRQ-UUNJERMWSA-N 0.000 description 1
- 239000001913 cellulose Substances 0.000 description 1
- 229920002678 cellulose Polymers 0.000 description 1
- 239000008120 corn starch Substances 0.000 description 1
- 239000002552 dosage form Substances 0.000 description 1
- GUBGYTABKSRVRQ-XLOQQCSPSA-N lactose Chemical compound O[C@@H]1[C@@H](O)[C@@H](O)[C@@H](CO)O[C@H]1O[C@@H]1[C@@H](CO)O[C@H](O)[C@H](O)[C@H]1O GUBGYTABKSRVRQ-XLOQQCSPSA-N 0.000 description 1
- 239000008101 lactose Substances 0.000 description 1
- 239000000243 solution Substances 0.000 description 1
- 239000012085 test solution Substances 0.000 description 1
Description
【特許請求の範囲】
【請求項1】 式
【化1】
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】 式
【化2】
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
-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
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.
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)
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 |
-
1998
- 1998-01-29 JP JP05412498A patent/JP4063386B2/en not_active Expired - Fee Related
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