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Sensitive Determination and Pharmacokinetic Study of Amlodipine in Human Serum by LC-ESI/MS/MS

机译:LC-ESI / MS / MS灵敏测定人血清氨氯地平并进行药代动力学研究

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摘要

A sensitive LC-ESI/MS/MS method was developed and validated to determine the concentrations of amlodipine in human serum. Amlodipine and the internal standard (IS) omeprazole were extracted from 200 μL of human serum by liquid-liquid extraction, using ethyl acetate as the extraction solvent. Sample analysis was performed by reversed-phase LC-MS/MS with electrospray ionization in positive ion mode, using selected reaction monitoring. The mobile phase composed of methanol and 0.15 % ammonium acetate in water (78 : 22, v/v) at a flow rate of 0.2 mL/min. The linearity ranged from 0.2 to 12.8 ng/mL. The extraction recoveries of amlodipine ranged from 90,68 to 105.27 %. The method was successfully used to pharmacokinetic study of amlodipine after an oral administration of 10 mg amlodipine tablets to 19 healthy volunteers.
机译:建立了灵敏的LC-ESI / MS / MS方法,并进行了测定人血清中氨氯地平的浓度的验证。氨氯地平和内标(IS)奥美拉唑以乙酸乙酯为萃取溶剂,通过液-液萃取从200μL人血清中萃取。样品分析是通过反相LC-MS / MS在正离子模式下采用电喷雾电离,并使用选定的反应监控进行的。流动相由甲醇和0.15%乙酸铵的水溶液(78:22,v / v)组成,流速为0.2 mL / min。线性范围为0.2至12.8 ng / mL。氨氯地平的提取回收率在90.68%至105.27%之间。在向19位健康志愿者口服10 mg氨氯地平片剂后,该方法已成功用于氨氯地平的药代动力学研究。

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