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A simple and rapid determination of biapenem in plasma by high-performance liquid chromatography

机译:高效液相色谱法快速简便地测定血浆中的比阿培南

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A simple, rapid and precise HPLC method using ultrafiltration to remove plasma protein was developed to determine biapenem concentrations in human plasma. Plasma was separated by centrifugation at 4 degrees C from blood collected in heparinized vacuum tubes, and biapenem was stabilized by immediate mixing the plasma with 1 M 3-morpholinopropanesulfonic acid (MOPS) buffer (pH 7.0) (1: 1). Biapenem was detected by ultraviolet absorbance at 300 nm with no interfering plasma peak. The calibration curve of biapenem in human plasma was linear from 0.04 to 50 mu g/mL. The limit of detection was 0.01 mu g/mL, which was more than 40-fold lower than that of conventional plasma protein precipitation using ammonium sulfate. The assay has been clinically applied to pharmacokinetic studies in patients. (c) 2006 Elsevier B.V. All rights reserved.
机译:开发了一种使用超滤去除血浆蛋白的简单,快速,精确的HPLC方法,以确定人血浆中的比阿培南浓度。通过在4摄氏度下离心从肝素化真空管中收集的血液中分离血浆,并通过立即将血浆与1 M 3-吗啉代丙烷磺酸(MOPS)缓冲液(pH 7.0)(1:1)混合来稳定比阿培南。比阿培南通过300 nm的紫外线吸收检测,没有干扰的血浆峰。比阿培南在人血浆中的校准曲线在0.04至50μg / mL之间呈线性关系。检测限为0.01μg / mL,比使用硫酸铵的常规血浆蛋白沉淀法低40倍以上。该测定法已临床应用于患者的药代动力学研究。 (c)2006 Elsevier B.V.保留所有权利。

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