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

被引:5
|
作者
Huo, Jiping [1 ,2 ]
Guo, Yangyang [3 ]
Zhang, Bo [4 ]
Zhao, Zhigang [1 ,2 ]
Shi, Guangzhi [5 ]
Mei, Shenghui [1 ,6 ]
机构
[1] Capital Med Univ, Beijing Tiantan Hosp, Dept Pharm, Beijing, Peoples R China
[2] Capital Med Univ, Coll Pharmaceut Sci, Dept Clin Pharmacol, Beijing, Peoples R China
[3] Capital Med Univ, Beijing Tiantan Hosp, Intens Care Unit, Beijing, Peoples R China
[4] Beijing Hlth Vocat Coll, Dept Pharm, Beijing, Peoples R China
[5] Capital Med Univ, Beijing Tiantan Hosp, Intens Care Unit, 119 Nansihuan West Rd, Beijing, Peoples R China
[6] Capital Med Univ, Beijing Tiantan Hosp, Dept Pharm, 119 Nansihuan West Rd, Beijing, Peoples R China
来源
JOURNAL OF MASS SPECTROMETRY | 2023年 / 58卷 / 06期
关键词
meropenem; moxalactam; norvancomycin; UHPLC-MS; MS; vancomycin; PRESSURE LIQUID-CHROMATOGRAPHY; HPLC; IMMUNOASSAY; VALIDATION; LATAMOXEF; SERUM;
D O I
10.1002/jms.4925
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
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 x 50 mm, 1.7 mu m) 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 mu g/mL for vancomycin, norvoncomycin, and meropenem; and 0.5-50 mu g/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.
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页数:11
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