A simple HPLC-UV Method for Therapeutic Drug Monitoring of Linezolid in human Plasma in low-resourced settings

V. A, S. V, Alffenaar Jw, Jeyakumar Sm, H. Ak
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引用次数: 2

Abstract

OBJECTIVE: A high-performance liquid chromatography method for the estimation of Linezolid in human plasma was developed and validated. METHODS: Samples (100µµL) were deproteinized with acetonitrile and analyzed using LiChrospher 100, RP18e column with PDA detection at 254 nm. The flow rate of the isocratic mobile phase comprising of 0.1% formic acid in 1000 ml of water and acetonitrile in the ratio of 60:40 (v/v) was set at 1.0 ml/min. RESULTS: The calibration curve ranged from 0.50 to 20.0 µg/ml and was linear. The recovery ranged from 96% to 101%. The accuracy ranged from 98 to 101% and intra- and inter-day relative standard deviation was <4.58%. The method reliably eliminated interfering materials from plasma and R2 was 0.9973. The method described was applied to the determination of plasma LZD concentration in multi-drug-resistant tuberculosis patients who are treated with a dose of 600 mg LZD once daily. CONCLUSIONS: The developed method is suitable for determination of plasma LZD in routine care and considered feasible in less-resourced settings
资源匮乏地区人血浆中利奈唑胺治疗药物监测的高效液相色谱-紫外分光光度法
目的:建立高效液相色谱法测定人血浆中利奈唑胺的含量。方法:用乙腈对样品(100µµL)进行脱蛋白处理,采用LiChrospher 100, RP18e色谱柱,在254 nm处进行PDA检测。0.1%甲酸与1000ml水、乙腈按60:40 (v/v)的比例组成的等密度流动相流速为1.0 ml/min。结果:标定曲线在0.50 ~ 20.0µg/ml范围内呈线性。回收率在96% ~ 101%之间。准确度为98 ~ 101%,日内、日间相对标准偏差<4.58%。该方法可靠地消除了等离子体中的干扰物质,R2为0.9973。本方法应用于多药耐药结核病患者血浆LZD浓度的测定,这些患者每天服用LZD 600 mg。结论:该方法适用于常规护理中血浆LZD的测定,在资源匮乏的环境中是可行的
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