A sensitive and high-throughput quantitative liquid chromatography high-resolution mass spectrometry method for therapeutic drug monitoring of 10 β-lactam antibiotics, linezolid and two β-lactamase inhibitors in human plasma.
Sarah Van VoorenAlain G VerstraetePublished in: Biomedical chromatography : BMC (2021)
An ultra-high pressure liquid chromatography high-resolution mass spectrometric (UHPLC-HRMS) method was developed for the simultaneous and sensitive quantification of 10 β-lactam antibiotics (cefepime, meropenem, amoxicillin, cefazolin, benzylpenicillin, ceftazidime, piperacillin, flucloxacillin, cefuroxime and aztreonam), linezolid and β-lactamase inhibitors tazobactam and clavulanic acid in human plasma. Validation according to the EMA guidelines showed excellent within- and between-run accuracy and precision (i.e. between 1.1 and 8.5%) and high sensitivity (i.e. lower limit of quantification between 0.25 and 1 mg/L). The UHPLC-HRMS method enables a short turnaround time and high sensitivity and needs only a small amount of plasma, allowing appropriate routine therapeutic drug monitoring. The short turnaround time is obtained by speeding up the protocol on multiple levels, i.e. fast and workload-efficient sample preparation (i.e. protein precipitation and dilution), short (4 min) instrument run time, simultaneous measurement of all relevant β-lactam antibiotics used in the intensive care unit and the use of the same instrument, column and mobile phases as for the other routine methods in our laboratory.
Keyphrases
- high resolution mass spectrometry
- liquid chromatography
- gram negative
- mass spectrometry
- tandem mass spectrometry
- high resolution
- ultra high performance liquid chromatography
- multidrug resistant
- gas chromatography
- simultaneous determination
- high throughput
- clinical practice
- solid phase extraction
- escherichia coli
- klebsiella pneumoniae
- liquid chromatography tandem mass spectrometry
- staphylococcus aureus
- methicillin resistant staphylococcus aureus
- small molecule
- protein protein
- patient reported outcomes
- molecularly imprinted
- amino acid
- single cell