LC-MS/MS法测定恒河猴血浆中巴替非班的浓度及药代动力学研究  被引量:3

Determination of batifeiban in macaque plasma by LC-MS/MS and its pharmacokinetic study

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作  者:李荣珊[1,2] 李全胜[2] 黄玉荣[2] 司端运[2] 刘昌孝[2] 

机构地区:[1]天津医科大学药学院天津市临床药物关键技术重点实验室,天津300070 [2]天津药物研究院释药技术与药代动力学国家重点实验室,天津300193

出  处:《中国新药杂志》2012年第15期1798-1802,共5页Chinese Journal of New Drugs

摘  要:目的:建立恒河猴血浆中巴替非班浓度的高效液相-串联质谱(Liquid Chromatography-TandemMass Spectrometry,LC-MS/MS)测定法,并研究其在恒河猴体内的药代动力学。方法:取恒河猴血浆200μL,加入含2μg.mL-1内标依替巴肽的乙腈-甲醇(70∶30)混合溶剂600μL沉淀蛋白,取上清液吹干,残留物加100μL流动相复溶,取上清液进行LC-MS/MS分析。色谱柱为ODS C18柱(150 mm×4.6 mm,5μm),流动相为甲醇-20 mmol.L-1甲酸铵(50∶50),流速为0.4 mL.min-1;质谱采用电喷雾离子化,正离子检测,巴替非班和内标的选择性检测离子分别为m/z 818.3→632.4和m/z 832.0→646.2。结果:巴替非班的线性范围为25~5 000 ng.mL-1,最低定量下限(lower limit of quantitation,LLOQ)为25 ng.mL-1,准确度、精密度及回收率均符合要求。结论:本方法专属性强,检测限低,灵敏度高,线性关系良好,方法简便快捷,适用于巴替非班临床前药代动力学研究。Objective: To develop a LC-MS/MS method for determination of batifeiban in macaque plasma, and to investigate the pharmacokinetics of batifeiban. Methods: Plasma samples 200μL were treated with 600 μL mixture of acetonitrile and methanol (70: 30, containing 2μg·mL(-1) of eptifibatide). After centrifugation to precipitate the proteins, the supernatant was evaporated under nitrogen gas flow at 40℃. Residues were dissolved in 100 μL of mobile phase and centrifuged at 12 000 r·min^(-1) for 5 min. Thereafter, 20 μL aliquots were injected into the LC-MS/MS for analysis. Separation was performed on a Diamonsil C18 column ( 150 mm x 4.6 mm, 5μm). The mobile phase was composed of methanol and 20 mmol·L^(-1) ammonium formate (50: 50). The selected reaction monitoring (SRM) transitions were performed at m/z 818.3→632.4 for batifiban and m/z 832.0→646.2 for eptifibatide (IS) in the positive ion mode with electrospray ionization (ESI) source. Results: Calibration curve was linear over the concentration range of 25 - 5 000 ng· mL^(-1). The lower limit of quantification was 25 ng·mL^(-1). The mean recovery was (65.7±4.9)%. The intra- and inter-day precisions were less than 5.3% and 14.0% , respectively, and the accuracy was within ±7.5%. Batifiban was stable in possible conditions of storing and han- dling. Conclusion: The method has been validated, and can be applied to determine the plasma concentration of batifiban for a pharmacokinetic study.

关 键 词:巴替非班 LC-MS/MS 恒河猴 血浆 药代动力学 

分 类 号:R969[医药卫生—药理学] R972.7[医药卫生—药学]

 

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