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布洛芬混悬液及其生物等效性研究[J]. 中国药科大学学报, 1997, (3): 11-16.
引用本文: 布洛芬混悬液及其生物等效性研究[J]. 中国药科大学学报, 1997, (3): 11-16.
Studies on Ibuprofen Suspension and Its Bioequivalence in Healthy Volunteers[J]. Journal of China Pharmaceutical University, 1997, (3): 11-16.
Citation: Studies on Ibuprofen Suspension and Its Bioequivalence in Healthy Volunteers[J]. Journal of China Pharmaceutical University, 1997, (3): 11-16.

布洛芬混悬液及其生物等效性研究

Studies on Ibuprofen Suspension and Its Bioequivalence in Healthy Volunteers

  • 摘要: 研制了布洛芬混悬液,分别建立了高效液相色谱法测定本品含量和血药浓度。以Advil混悬液为对照比较了本品的质量。以布洛芬片剂为对照,研究了本品在10名健康志愿受试者体内的药物动力学。结果表明:本品和Advil混悬液的相对密度分别为1.15和1.18;本品在人体内的动力学为—房室模型,本品的相对生物利用度为107.16%±8.32%。本品吸收快、达峰时间短、峰浓度高,与布洛芬片剂比较有显著性差异。LnAUC值经双单侧与等效性检验和(1一2d)置信区间等效性试验,结果表明两种制剂为生物等效制剂。

     

    Abstract: Ibuprofen suspension(100 mg/5 ml) was prepared according to the Children's Advil suspension. Two simple and sensitive high performance liquid chromatographic methods were established and could be seperately used for the analysis of suspension quality and

     

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