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作 者:王永升[1] 赵小平[1] 钟皎[1] 陈燕 柳晓泉[1] 王广基[1]
机构地区:[1]中国药科大学药物代谢与动力学研究中心,南京210009
出 处:《中国药科大学学报》2006年第2期146-149,共4页Journal of China Pharmaceutical University
基 金:国家高技术研究发展计划("八六三"计划)资助项目(NO.2003AA2Z347A);江苏省药物代谢动力学重点实验室资助项目(No.BM2001201)~~
摘 要:目的:建立测定比格犬血浆中吡非尼酮浓度的方法,用于研究其在比格犬体内的药代动力学。方法:血浆样品用10%高氯酸沉淀蛋白后取上清液直接进样,采用HPLC-UV法测定。色谱柱为汉邦Liehtospher C18柱(250mm×4.6mm ID,5μm),流动相为乙腈.0.2%醋酸水(23:77),流速1.0mL/min,检测波长310nm,内标为水杨酸。结果:线性范围为0.075~76.67班,方法回收率在100.2%~103.3%之间,日内和日间的精密度均小于6%。结论:该方法样品前处理过程简便,灵敏度高,重现性好,符合血浆样品的测定要求,可应用于吡非尼酮比格犬体内的药代动力学研究。Aim:To develop a HPLC-UV method for the determination of pirfenidone in Beagle dog's plasma and for the studies of its pharmaeokinetics in Beagle dogs. Methods: Plasma was precipitated with perehlorie acid (10%) after addition of the internal standard salicylic acid, and the upper aliquot was directly injected onto HPLC system. Separation was achieved on a Liehrospher C18 column (250 mm× 4.6 mm ID, 5 μm) with the mobile phase of aeetonitrile-water containing 0.2% acetic acid (23:77) ,at a flow-rate of 1 mL/min. The eluent was detected at 310 nm. ReSults: Linear detection responses for pirfenidone in the plasma were obtained for prifenidone concentration ranging from 0.075 to 76.67μg/mL. The precision data, based on intra- and inter-day variations over 5 days, were lower than 6% and the mean recoveries of prifenidone ranged from 100.2% to 103.3 %. Conclusion:The established HPLC method is simple, sensitive, reliable and applicable for pharmaeokinetie studies of pirfenidone.
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