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反相高效液相色谱法测定人血清中奈韦拉平浓度 被引量:2

Determination of serum nevirapine by RP-HPLC
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摘要 目的:建立RP-HPLC法测定人血清中奈韦拉平的浓度.方法:以盐酸左氧氟沙星为内标,色谱条件:ZORBAX Eclipse XDB-C8色谱柱(150 mm×4.6 mm,5μm),流动相为15 mmol·L-1磷酸氢二铵溶液(pH=7.5)-乙腈(80:20);流速1.5 mL·min-1;检测波长295 nm.结果:线性范围为0.05~8μg·mL-1,相关系数r=0.999 3.结论:测定方法简便、准确、专属性好. Objective: To establish a RP-HPLC method to assay serum nevirapine. Methods: The HPLC conditions were as follows: ZORBAX Eclipse XDB-C8 column (4.6 mm × 150 mm, 5 μm), the mobile phase consisted of 15 mmol· L^-1 (NH4)2HPO4 (pH 7.5 adjusted by phosphate acid)-acetonitrile (80:20) with the flow rate of 1.5 mL·min^-1 and the detection wavelength at 295 nm. Levofloxacin was used as an internal standard. Results: The linear curve was in the range of 0.05 - 8 μg·mL^-1 ( r=0. 999 3 ). Conclusion: The RP-HPLC method is simple, accurate and reliable.
出处 《中国新药杂志》 CAS CSCD 北大核心 2005年第9期1178-1180,共3页 Chinese Journal of New Drugs
关键词 奈韦拉平 反相高效液相色谱法 血清药物浓度 nevirapine reversed phase-high performance liquid chromatography (RP-HPLC) serum concentration
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