セファレキシンカプセルの品質試験
書誌事項
- タイトル別名
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- Quality Test of Sephalexin Capsules
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説明
The quality of 6 brands of cephalexin capsules (250mg) was evaluated by dissolution test (U. S. P. XIX) and some other tests in vitro. The dissolution rate of 1 (product F) of the 6 kinds of capsules was about 57% in the first 15 minutes, showing a statistically significant difference (p<0. 01) between the rates (nearly 100%) for the remaining 5. Further, the variations of weight, content and dissolution rate were larger in product F than in the others. The rate of in vitro dissolution may be a decisive factor in the in vivo absorption and excretion. From the viewpoint of uniformity of therapeutic effect, product F is undesirable.
収録刊行物
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- 病院薬学
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病院薬学 2 (3), 154-158, 1976
一般社団法人 日本医療薬学会
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詳細情報 詳細情報について
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- CRID
- 1390282679752281344
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- NII論文ID
- 110001796631
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- NII書誌ID
- AN00002794
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- ISSN
- 21859477
- 03899098
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- データソース種別
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- JaLC
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- NDLデジコレ(旧NII-ELS)
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