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一种用于临床应用的通过超高效液相色谱/串联质谱法快速测定人尿中22种选定药物的方法。

A rapid method for determination of 22 selected drugs in human urine by UHPLC/MS/MS for clinical application.

作者信息

Magiera Sylwia, Baranowska Irena

出版信息

J AOAC Int. 2014 Nov-Dec;97(6):1526-37. doi: 10.5740/jaoacint.13-333.

Abstract

A rapid and sensitive ultra-HPLC/MSIMS (UHPLC/MSIMS) assay method for the simultaneous determination in human urine of 22 drugs belonging to different pharmaceutical groups was developed. The drugs were extracted from urine samples and then separated on a Zorbax Rapid Resolution High Definition SB-C18 column. The mobile phase consisted of methanol and water containing formic acid with gradient elution. The chromatographic separation time was 7 min. The MSIMS detector, equipped with an electrospray ionization source, was set up in both positive and negative modes. The lower LOQs for the drugs in this method were between 0.05 and 0.60 ng/mL. Calibration curves in human urine were generated in the range of 0.05-600 ng/mL. Method validation parameters such as intraday and interday precision, accuracy, extraction recovery, stability, selectivity, dilution integrity, and carryover effect for all the compounds were within the acceptable ranges. This simple and fast method was applied successfully to study the pharmacokinetics of four selected drugs in human urine collected from patients. This UHPLC/MS/MS method offers an attractive way forward for the development of a routine rapid analysis for selected substances, particularly given the growing amount of new information about drug properties.

摘要

建立了一种快速灵敏的超高效液相色谱/质谱联用(UHPLC/MSIMS)分析方法,用于同时测定人尿中22种属于不同药物类别的药物。药物从尿液样本中提取,然后在Zorbax快速分离高分辨SB-C18柱上进行分离。流动相由含甲酸的甲醇和水组成,采用梯度洗脱。色谱分离时间为7分钟。配备电喷雾电离源的MSIMS检测器以正、负两种模式进行设置。该方法中药物的最低定量限在0.05至0.60 ng/mL之间。在人尿中生成了0.05 - 600 ng/mL范围内的校准曲线。所有化合物的方法验证参数,如日内和日间精密度、准确度、提取回收率、稳定性、选择性、稀释完整性和残留效应,均在可接受范围内。这种简单快速的方法成功应用于研究从患者收集的人尿中四种选定药物的药代动力学。这种UHPLC/MS/MS方法为选定物质的常规快速分析开发提供了一种有吸引力的途径,特别是考虑到关于药物性质的新信息不断增加。

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