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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。安莫西林(Amoxicillin)口服膠囊製劑共50件，其中國產47件，進口3件。依據U.S.P.XXII之高效液相層析法(High Performance Liquid chromatograph)、日本抗生物質醫藥品基準解說(MRAP)上所載之分光光度法及微生物法測定其力價，結果有4件未達合格標準，不合格率為8.0%。
英文摘要
In order to understand the potency of amoxicillin capsules, fifty samples (47 domestic, 3 imported) were purchased from different counties and cities in Taiwan during September 1990 to March 1991. All of the samples were determin performance liquid chromatographic method, the cylinder-plate method and optical method as described in the United State Pharmacopeia and the Minimum Requirements for Antibiotic Products of Japan. The results showed that 4 samples (8.0%) failed to meet the potency requirement of the government regulation (90-120%).