文章詳目資料
藥物食品檢驗局調查研究年報
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中文摘要
本計畫於民國80年度，由全省各縣市抽購國產及進口安比西林(Ampicillin)。服膠囊製劑共50件，其中國產46件，進口4件。依據U.S.P. XXII之高效液相析法(High Performance Liquid chromatograph)，日本抗生物質醫藥品慕準解說(MRAP)上所載之分光光度法及微生物法測定其力價，結果有5件未達合格標準，不合格率為10.0%。
英文摘要
In order to understand the potency of ampicillin capsules, fifty samples (46 domestic, 4 imported) were purchased from different counties and cities in Taiwan during September 1990 to March 1991. All of the samples were deter-minecylinder-plate method and optical method as described in Minimum Requirements for Antibiotic Products of Japan. The results showed that 5 samples (10.0%) failed to meet the potency requirement of the government regulation (90-120%).