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尼美舒利3种制剂的药代动力学研究
引用本文:张先洲,马福旺,李荣凌.尼美舒利3种制剂的药代动力学研究[J].中国药师,1999,2(4):173-174.
作者姓名:张先洲  马福旺  李荣凌
作者单位:湖北医科大学附一院药学部,湖北医科大学附一院药学部,湖北医科大学附一院药学部,湖北医科大学附一院药学部,湖北医科大学附一院药学部 武汉 430060,武汉 430060,武汉 430060,武汉 430060,武汉 430060
摘    要:目的:测定尼美舒利在兔体内药物代谢动力学过程,比较片剂、混悬剂、栓剂的药动学参数。方法:用高效液相色谱法测定血浆中尼美舒利浓度,用3P87程序处理血药浓度数据。结果:片剂与混悬剂的药动学参数无显著性差异(P>0.05),栓剂的T_(max)、t1/2ke明显长于片剂和混悬剂,相对于片剂的生物利用度为79.9%,相对于混悬剂的生物利用度为74.5%。

关 键 词:尼美舒利  片剂  混悬剂  栓剂  药代动力学  生物利用度

Study on Pharmacokinetics of Three Preparations from Nimesulide
Zhang Xianzhou,Ma Fuwang,Li Rongling,Luo Shunde,Cai Hongsheng.Study on Pharmacokinetics of Three Preparations from Nimesulide[J].China Pharmacist,1999,2(4):173-174.
Authors:Zhang Xianzhou  Ma Fuwang  Li Rongling  Luo Shunde  Cai Hongsheng
Institution:Zhang Xianzhou,Ma Fuwang,Li Rongling,Luo Shunde,Cai Hongsheng Department of Pharmacy,The First Affiliated Hospital of Hubei Medical University,Wuhan 430060,P. R. China
Abstract:Objective: To study the pharmacokinetics properties and pharmacokinetic parameters of nimesulide in tablet, suspension, and suppository. Method: The plasma concentration of nimesulide was determined by HPLC. the data was treated with 3p87 procdeure. Result: There was a significant difference in the pharmacokinetics parameters between ninesulide tablet and nime-sulid suspension. tmax, t1/2ke of suppository were longer than that of tablet and suspension. The bioavailability of suppository to tablet was 79.9 % and to suspension 74.5 % .
Keywords:Nimesulide  Tablet  Suspension  Suppository  Pharmacokinetics  Bioavailability
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