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

Author:

Huo Jiping12ORCID,Guo Yangyang3,Zhang Bo4,Zhao Zhigang12,Shi Guangzhi,Mei Shenghui1

Affiliation:

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

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

3. Intensive Care Unit, Beijing Tiantan Hospital Capital Medical University Beijing China

4. Department of Pharmacy Beijing Health Vocational College Beijing China

Abstract

AbstractWe 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.

Funder

National Key Research and Development Program of China

Publisher

Wiley

Subject

Spectroscopy

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