首页> 外文期刊>Journal of chromatography, B. Analytical technologies in the biomedical and life sciences >High performance liquid chromatographic determination of plasma free and total tazobactam and piperacillin
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High performance liquid chromatographic determination of plasma free and total tazobactam and piperacillin

机译:高效液相色谱法测定血浆中游离他唑巴坦和总他唑巴坦和哌拉西林的含量

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A high-pressure liquid chromatography (HPLC) method with ultraviolet detection was developed for the measurement of plasma free and total tazobactam and piperacillin. This method is simple and fast, requiring only 11 min for the HPLC run and a sample preparation of about 11 min for total drugs and 10min for free drugs. The procedure for the assay involves the treatment of plasma with acetonitrile for total drugs determination, and the use of a centrifugal filter device to deproteinize plasma for free drugs determination. The HPLC column, a Hypersil-ODS, was equilibrated with an eluent mixture composed of acetonitrile-potassium phosphate (pH 2.6). CVs for repeatability of tazobactam and piperacillin measurements ranged from 4.30 to 6.60; CVs for reproducibility ranged from 5.60 to 9.40. Mean analytical recoveries ranged from 100.4 to 103%. A linear relationship was obtained between peak area and drugs concentration in the range studied (0-62.5 mg/L for tazobactam and 0-500 mg/L for piperacillin). The equation for regression line were y = 19x - 1.4 for tazobactam and y = 1.7x - 0.9 for piperacillin; correlation coefficients were > 0.999. The lower limit of quantitation (LLQ) for standard samples was about 0.12 mg/L for tazobactam and 0.49 mg/L for piperacillin, respectively. The lower limit of detection (LLD)was 0.06 mg/L for tazobactam and 0.24 mg/L for piperacillin. This HPLC assay for tazobactam and piperacillin is sensitive and accurate, and provides a reliable determination of both free and total tazobactam and piperacillin in human plasma, thus allowing the determination of these analytes in patients receiving tazocillin therapy.
机译:建立了一种具有紫外检测功能的高压液相色谱(HPLC)方法,用于测量血浆中游离他唑巴坦和总他唑巴坦和哌拉西林的含量。该方法简单,快速,HPLC运行仅需11分钟,总药物约11分钟,游离药物约10分钟。该测定方法包括用乙腈处理血浆以测定全部药物,并使用离心过滤器对血浆进行脱蛋白以测定游离药物。 HPLC色谱柱Hypersil-ODS用乙腈-磷酸钾(pH 2.6)组成的洗脱液混合物平衡。他唑巴坦和哌拉西林测定的重复性CV在4.30至6.60之间;重现性的CV在5.60至9.40之间。平均分析回收率在100.4%至103%之间。在研究范围内(塔唑巴坦为0-62.5 mg / L,哌拉西林为0-500 mg / L),峰面积与药物浓度之间存在线性关系。他唑巴坦的回归线方程为y = 19x-1.4,哌拉西林的y = 1.7x-0.9。相关系数> 0.999。标准样品的他唑巴坦定量下限(LLQ)分别为约0.12 mg / L和哌拉西林0.49 mg / L。他唑巴坦的最低检测限(LLD)为0.06 mg / L,哌拉西林的最低检测限为0.24 mg / L。 HPLC测定他唑巴坦和哌拉西林的灵敏度高,准确度高,并且可以可靠地测定人血浆中游离和总他唑巴坦和哌拉西林的含量,从而可以测定接受他唑西林治疗的患者中的这些分析物。

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