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一种 UHPLC-MS/MS 法同时测定人血浆中万古霉素、去甲万古霉素、美罗培南和莫西沙星的浓度及其临床应用。

A UHPLC-MS/MS method for the simultaneous determination of vancomycin, norvancomycin, meropenem, and moxalactam in human plasma and its clinical application.

机构信息

Department of Pharmacy, Beijing Tiantan Hospital, Capital Medical University, Beijing, China.

Department of Clinical Pharmacology, College of Pharmaceutical Sciences, Capital Medical University, Beijing, China.

出版信息

J Mass Spectrom. 2023 Jun;58(6):e4925. doi: 10.1002/jms.4925.

Abstract

We developed an ultra-high-performance liquid chromatography-tandem mass spectrometry (UHPLC-MS/MS) method to determine four antibacterial drugs in human plasma for clinical usage. Samples were prepared using protein precipitation with methanol. Chromatographic separation was accomplished in 4.5 min on a BEH C18 column (2.1 × 50 mm, 1.7 μm) using a gradient elution of methanol and water (containing 7.71 g/L concentrated ammonium acetate, adjusted to pH 6.5 with acetic acid) at a flow rate of 0.4 mL/min. Positive electrospray was used for ionization. The method was linear in the concentration range 1-100 μg/mL for vancomycin, norvoncomycin, and meropenem; and 0.5-50 μg/mL for R-isomer of moxalactam and S-isomer of moxalactam. For all analytes, the intra- and inter-day accuracies and precisions were -8.47%-10.13% and less than 12%, respectively. The internal standard normalized recoveries and matrix effect were 62.72%-105.78% and 96.67%-114.20%, respectively. All analytes were stable at six storage conditions, with variations of less than 15.0%. The method was applied in three patients with central nervous system infection. The validated method might be useful for routine therapeutic drug monitoring and pharmacokinetic study.

摘要

我们开发了一种超高效液相色谱-串联质谱(UHPLC-MS/MS)方法,用于测定人血浆中的四种抗菌药物,以用于临床应用。样品采用甲醇沉淀蛋白法制备。在 BEH C18 柱(2.1×50mm,1.7μm)上,以甲醇和水(含 7.71g/L 浓乙酸铵,用乙酸调至 pH6.5)为流动相,采用梯度洗脱,流速为 0.4mL/min,实现了 4.5min 的色谱分离。采用正电喷雾进行离子化。万古霉素、去甲万古霉素和美罗培南的浓度在 1-100μg/mL 范围内,R-异构体莫西沙星和 S-异构体莫西沙星的浓度在 0.5-50μg/mL 范围内呈线性。对于所有分析物,日内和日间准确度和精密度分别为-8.47%-10.13%和小于 12%。内标归一化回收率和基质效应分别为 62.72%-105.78%和 96.67%-114.20%。所有分析物在六种储存条件下均稳定,变化小于 15.0%。该方法已应用于三名中枢神经系统感染患者。经验证的方法可能对常规治疗药物监测和药代动力学研究有用。

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