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作 者:谢建芬[1,2] 陈荣[2] 夏宗玲[2] 丁选胜[1]
机构地区:[1]中国药科大学临床药学教研室,南京市210009 [2]江苏常州市第一人民医院药剂科,常州市213003
出 处:《中国药房》2011年第10期889-890,共2页China Pharmacy
摘 要:目的:建立测定人血清中细胞色素P4503A4(CYP3A4)探针药物氨苯砜浓度的方法。方法:采用高效液相色谱法,色谱柱果为迪:氨马苯D砜ia血mo药ns浓ilC度18在,流1动~相6m为g.乙L腈-1-范水(围2内5:线75性),关流系速良为好1(.0rm=L0..9m9i9n-1)1,;紫方外法检回测收波率长为为942.5985%nm~,柱10温2.7为7%30,℃日,内进、样日量间为RS30Dμ分L别。≤结7.05%、5.54%。结论:本方法快速、准确、灵敏度高、专属性强,适用于人血清中氨苯砜浓度的测定。OBJECTIVE: To establish the method for determination of cytochrome P4503A4 (CYP3A4)probe drug dapsone in human serum by HPLC. METHODS: HPLC method was adopted. The determination was performed on Diamonsil C18 column with mobile phase consisted of acetonitrile-water (25 : 75) at flow rate of 1.0 mL. min^-1. UV detection wavelength was set at 258 nm and the column temperature was 30℃. The irdection volume was 30μL. RESULTS: The linear range of dapsone were 1-6 mg.L^-1(r= 0,999 1) with recovery rate of 94.95%-102,77%, The RSD of intra-day and inter-day were less than 7.05% and 5,54%, CONCLUSION: The method is rapid, accurate, sensitive and specific for concentration determination of dapsone in human serum.
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