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Simultaneous quantification of lidocaine and prilocaine in human plasma by LC-MS/MS and its application in a human pharmacokinetic study

机译:LC-MS / MS同时定量测定人血浆中利多卡因和丙胺卡因的含量及其在人体药代动力学研究中的应用

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ObjectiveThe aim of the work was to develop and validate a simple, sensitive and selective Liquid chromatography with Mass spectroscopic method for simultaneous quantification of lidocaine and prilocaine in human plasma.Design and methodsAnalytes and the internal standards from human plasma were extracted by using solid- phase extraction technique using Waters Oasis? HLB 1??cc (30??mg) cartridges. The reconstituted samples were chromatographed on Phenomenex Kinetex EVO 4.6*100??mm 2.6 μ 100A column by using a mixture of acetonitrile and 5??mM ammonium acetate buffer (80:20, v/v) as the mobile phase at a flow rate of 0.6??mL/min.ResultsThe method was validated over the concentration range of 0.10–201.80?ng/mL for lidocaine and 0.10–201.66?ng/mL for prilocaine. The calibration curve obtained was linear.ConclusionMethod validation was performed as per FDA guidelines and the results met the acceptance criteria. A run time of 3.0?min for each sample, make it possible to analyze more than 350 human plasma samples per day. The proposed method was found applicable for pharmacokinetic studies.
机译:目的本工作的目的是开发和验证一种简单,灵敏,选择性的液相色谱-质谱联用技术,可同时定量人血浆中的利多卡因和丙胺卡因。设计和方法采用固相提取人血浆中的分析物和内标使用沃特世绿洲提取技术? HLB 1?cc(30?mg)滤芯。重建的样品在Phenomenex Kinetex EVO 4.6 * 100 ?? mm 2.6μ100A色谱柱上,通过使用乙腈和5?mM醋酸铵缓冲液(80:20,v / v)的混合物作为流动相进行色谱分离结果为0.6 ?? mL / min。结果在利多卡因0.10–201.80?ng / mL和丙胺卡因0.10–201.66?ng / mL的浓度范围内验证了该方法。获得的校准曲线是线性的。结论根据FDA指南进行方法验证,结果符合接受标准。每个样品的运行时间为3.0分钟,因此每天可以分析350多个人体血浆样品。发现提出的方法可用于药代动力学研究。

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