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建立并验证一种灵敏、简单的 LC-MS/MS 法,用于人血浆中氨苄西林和舒巴坦的定量分析,并将其应用于临床药代动力学研究。

Development and validation of a simple and sensitive LC-MS/MS method for quantification of ampicillin and sulbactam in human plasma and its application to a clinical pharmacokinetic study.

机构信息

Division of Pharmaceutics and Translational Therapeutics, College of Pharmacy, University of Iowa, USA.

College of Pharmacy, University of Iowa, USA.

出版信息

J Pharm Biomed Anal. 2021 Mar 20;196:113899. doi: 10.1016/j.jpba.2021.113899. Epub 2021 Jan 15.

Abstract

Ampicillin-sulbactam is a broad-spectrum combination antibiotic used for a variety of clinical applications, including as a prophylactic agent to reduce the risk of surgical site infection. The pharmacokinetics of ampicillin-sulbactam after redosing during prolonged surgeries remains incompletely understood. In anticipation of further studying the intra-operative pharmacokinetics of this drug, we have developed a novel liquid chromatography-tandem mass spectrometry (LC-MS/MS) method for the quantification of ampicillin and sulbactam. The plasma samples were prepared using a simple protein precipitation method. Gradient chromatographic elution was used to separate analytes, and MS/MS analysis was performed in negative ionization mode for both analytes via multiple reaction monitoring (MRM). All validation parameters were evaluated under a good laboratory practice (GLP) environment. For both ampicillin and sulbactam, the lower limit of quantitation (LLOQ) was established as 0.25 μg/mL. The calibration curve ranged from 0.25 to 200 μg/mL for ampicillin and 0.25-100 μg/mL for sulbactam. Inter- and intra-day precisions for both analytes were ≤11.5 % for quality controls and ≤17.4 % for LLOQ; accuracies ranged from -11.5 to 12.5% for 3 quality control levels and -18.1-18.7% for LLOQ. In addition to sensitivity, accuracy and precision, 13 other parameters were also validated for both analytes, and the results met the acceptance criteria. Our method was successfully applied to quantify ampicillin and sulbactam concentrations in patients undergoing surgery.

摘要

氨苄西林-舒巴坦是一种广谱联合抗生素,用于多种临床应用,包括作为预防剂以降低手术部位感染的风险。在长时间手术中再次给药后氨苄西林-舒巴坦的药代动力学仍不完全了解。为了进一步研究这种药物的术中药代动力学,我们开发了一种新的液相色谱-串联质谱(LC-MS/MS)方法来定量检测氨苄西林和舒巴坦。使用简单的蛋白质沉淀法制备血浆样品。采用梯度洗脱色谱法分离分析物,通过多反应监测(MRM)在负离子模式下对两种分析物进行 MS/MS 分析。所有验证参数均在良好实验室规范(GLP)环境下进行评估。对于氨苄西林和舒巴坦,定量下限(LLOQ)均设定为 0.25μg/mL。氨苄西林的校准曲线范围为 0.25-200μg/mL,舒巴坦的校准曲线范围为 0.25-100μg/mL。两种分析物的日内和日间精密度均为质控品≤11.5%,LLOQ≤17.4%;准确度为 3 个质控水平为-11.5%至 12.5%,LLOQ 为-18.1%至-18.7%。除了灵敏度、准确度和精密度外,还对两种分析物的 13 个其他参数进行了验证,结果符合验收标准。我们的方法成功地应用于定量检测手术患者的氨苄西林和舒巴坦浓度。

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