An LC–MS–MS method for the simultaneous quantification of amoxicillin and clavulanic acid in human plasma and its pharmacokinetic application

Avinash Gaikwad , Sumit Gavali , Narendiran , Deepak Katale , Shantaram Bonde , Ranjana Praveen Bhadane
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引用次数: 14

Abstract

Objective

To develop a simple, sensitive and selective LC–MS–MS method for the simultaneous determination of amoxicillin and clavulanic acid in human plasma using amoxicillin D4 and ampicillin as internal standard (IS).

Method

Amoxicillin and clavulanic acid in plasma were concentrated by solid phase extraction and chromatographed on a C18 column using a mobile phase of acetonitrile: 2 mM ammonium acetate (80:20 v/v) under isocratic condition. Quantitation was performed on a triple quadrupole mass spectrometer by employing electrospray ionization technique and operating in multiple reaction monitoring (MRM) and negative ion mode with mass transitions 364.00/223.00, 198.00/136.00, 368.00/227.00 and 347.90/304.00 for Amoxicillin, Clavulanic acid, Amoxicillin D4 and Ampicillin respectively.

Results

The method was validated over a linear range of 50.43–31500.68 and 25.28–6185.18 ng/mL for amoxicillin and clavulanic acid respectively. The Lower Limit of Quantitation (LLOQ) were 50.43 and 25.28 ng/mL for amoxicillin and clavulanic acid respectively. Inter-batch and intra-batch coefficient of variation across three validation runs (LLOQ, LQC, MQC1, MQC and HQC) was less than 3.55% and 3.07% for amoxicillin and clavulanic acid respectively.

Conclusion

The method was validated and was suitable for the quantitation of amoxicillin and clavulanic acid from plasma samples in a pharmacokinetic study.

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LC-MS-MS同时定量人血浆中阿莫西林和克拉维酸的方法及其药动学应用
目的建立以阿莫西林D4和氨苄西林为内标(IS)同时测定人血浆中阿莫西林和克拉维酸含量的LC-MS-MS方法。采用固相萃取法浓缩血浆中的甲氧莫西林和克拉维酸,在C18色谱柱上,以乙腈:2 mM醋酸铵(80:20 v/v)为流动相,等温条件下进行色谱分析。阿莫西林、克拉维酸、阿莫西林D4和氨苄西林的质量跃迁分别为364.00/223.00、198.00/136.00、368.00/227.00和347.90/304.00,采用电喷雾电离技术,在多重反应监测(MRM)和负离子模式下进行定量。结果阿莫西林和克拉维酸在50.43 ~ 31500.68和25.28 ~ 6185.18 ng/mL的线性范围内有效。阿莫西林和克拉维酸的定量下限分别为50.43和25.28 ng/mL。阿莫西林和克拉维酸三个验证运行(LLOQ、LQC、MQC1、MQC和HQC)的批间和批内变异系数分别小于3.55%和3.07%。结论该方法适用于血浆样品中阿莫西林和克拉维酸的药动学定量研究。
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