首页> 外文期刊>Indian journal of pharmacology. >A validated high-performance liquid chromatography method for the determination of rifampicin and desacetyl rifampicin in plasma and urine
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A validated high-performance liquid chromatography method for the determination of rifampicin and desacetyl rifampicin in plasma and urine

机译:经验证的高效液相色谱法测定血浆和尿液中的利福平和去乙酰利福平

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Objective: To standardize a high-performance liquid chromatography (HPLC) method for the determination of rifampicin (RMP) and its major metabolite desacetyl rifampicin (DRMP) in plasma and urine.Material and Methods: A simple, specific and sensitive HPLC method was developed for the determination of RMP and DRMP in plasma and urine. Separation in both was achieved by reverse-phase chromatography on a C_(18) column with a mobile phase composition of 0.05 M phosphate buffer: acetonitrile (55:45 v/v) at 254 nm.Results: The retention times of DRMP, RMP and Rifapentine (RPN), the internal standard were 2.9, 4.8 and 10.5 min respectively. The assay was linear from 0.25 to 1 5.0 mug ml~(-1) for plasma and 2.5 to 80.0 |ig ml1 for urine. Both intra-day and inter-day accuracy and precision data showed good reproducibility.Conclusion: The HPLC method described is sensitive, selective and linear for the wide range of concentrations for RMP and DRMP in plasma and urine. Thus, the method developed is well suited for the phamnacokinetic studies.
机译:目的:标准化高效液相色谱法测定血浆和尿液中的利福平(RMP)及其主要代谢产物去乙酰利福平(DRMP)。材料与方法:建立了一种简单,特异且灵敏的HPLC方法用于测定血浆和尿液中的RMP和DRMP。在C_(18)色谱柱上进行反相色谱分离,在254 nm下流动相组成为0.05 M磷酸盐缓冲液:乙腈(55:45 v / v),从而实现了两种分离。结果:DRMP,RMP的保留时间内标分别为2.9、4.8和10.5分钟。该测定的血浆线性范围为0.25至1 5.0毫升/毫升,尿液为2.5至80.0微克/毫升。日间和日间精度和精密度数据均显示出良好的重现性。结论:所描述的HPLC方法对血浆和尿液中RMP和DRMP的多种浓度均具有灵敏,选择性和线性的特点。因此,开发的方法非常适合于药物动力学研究。

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