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作 者:李扬[1] 王威[1] 王汝卫 刘蕾[1] 史爱欣[1] 赫广威[1] 李可欣[1] 孙春华[1] 宋友华[1]
机构地区:[1]卫生部北京医院临床药理基地,北京100730 [2]宁夏煤炭职工医院,753000
出 处:《中国临床药理学杂志》2000年第2期129-131,共3页The Chinese Journal of Clinical Pharmacology
摘 要:12名健康志愿者采用交叉给药方法,分别单剂量口服5mg国产盐酸阿呋唑嗪片及进口盐酸阿呋唑嗪片,进行两种制剂的生物等效性研究。采用HPLC荧光检测法测定血浆中阿味唑嗪的浓度,血药浓度-时间数据经3p97生物利用度计算程序处理拟合,符合血管外给药二室开放模型,试验结果表明:单次口服5mg国产盐酸阿呋唑嗪片和进口盐酸阿呋唑嗪片后,达峰时间分别为146 ± 0.54h和1.42 ±0.29 h,峰浓度分别为 39.79 ± 5,29 μ g· L^(-1)和 40.05 ± 5.88 μ g· L^(-1),0- 24h的药时曲线下面积分别为225.40 ± 26.66μg·h· L^(-1)和235.04±24.13 μ g·h· L^(-1)、其主要药代动力学参数经方差分析和双单侧t检验,无显著性差异(P>0.05),两种制剂具有生物等效性。国产盐酸阿呋唑嗪片的相对生物利用度为96.90/±15.8%。The relative bioavailability and pharmacokinetics of domestic alfuzosin tablets were studied in 12 healthy male volunteers.A dose of sing of domestic or imported alfuzosin hydrochloride was given according to a randomized 2 cross-over design,blood samples were withdrawn up to 24 hours post administration,and plasma concentration of alfuzosin was determined by high performance liquid chromatography (HPLC) flavoxate.The concentration-time curves of two preparations were fitted to a two-compartment model.The peak plasma levels(C_(max))of alfuzosin hydrochloride domestic drug and imported drug were 39.79 ± 5.29 and 40.05 ± 5.88 p g·L^(-1) respectively,the peak time (T_(max))were 1.46 ± 0.54h and 1.42 ± 0.29h respectively,and AUC(O-24) were 225.40 ± 26.66 and 235.04 ± 24. 13 μg· h·L^(-1)respectively.The pharmacokinetics and relative bioavailability data obtained in the study furnished definite proof of bioequivalence of both domestic and imported alfuzosin hydrochloride tablets.
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