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盐酸曲马多缓释片的人体药代动力学及相对生物利用度
引用本文:刘会臣 胡玉钦. 盐酸曲马多缓释片的人体药代动力学及相对生物利用度[J]. 中国药房, 1999, 10(4): 170-171
作者姓名:刘会臣 胡玉钦
作者单位:白求恩国际和平医院临床药理室!石家庄市050082
摘    要:目的:研究两种盐酸白马多缓释片的药代动力学及相对生物利用度。方法:随机交叉试验设计,健康志愿者口服单剂量和多剂量盐酸曲马多缓释片,气相色谱法测定血清中盐曲马多的浓度。结果:两药AUCo—t、Tmax、Cmax等药代动力学参数均无显著性差异。结论:两药具有生物等效性。

关 键 词:盐酸曲马多缓释片  药代动力学  相对生物利用度  气相色谱

Clinical Pharmacokinetics and Relative Bioavailability of Tramadol Hydrochloride Sustained-released Tablets
LIU Huichen, HU Yuqin, WANG Jian,LI Xinfang, HOU Yanning. Clinical Pharmacokinetics and Relative Bioavailability of Tramadol Hydrochloride Sustained-released Tablets[J]. China Pharmacy, 1999, 10(4): 170-171
Authors:LIU Huichen   HU Yuqin   WANG Jian  LI Xinfang   HOU Yanning
Abstract:OBJECTIVE:To study the clinical pharmacokinetics and relative bioavailability of two kinds of tramadol hydrochloride sustained-released tablets.METHOD:In a randomized cross-overdesign,the study was carried out in healthy volunteers after asingle oral dose and multiple oral doses.The serum concentrations oftramadol hydrochloride were measured by gas chromatography. RESULTS: There were no significant differences in all pharmacokineticparameters between two preparations,expecially AUCo-t,Tmax and Cmax.CONCLUSION:The two preparations were bioequivalent.
Keywords:tramadol hydrochloride sustained-released tablet  pharmacokinetics  relative bioavailability  gas chromatography.
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