4.5 Article

Automated HPLC-MS/MS assay for the simultaneous determination of ten plasma antibiotic concentrations

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ELSEVIER
DOI: 10.1016/j.jchromb.2022.123496

Keywords

TDM; Antibiotics; Automated sample preparation; LC-MS; MS

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Therapeutic drug monitoring (TDM) is crucial for patients with serious bacterial infections in order to optimize treatment efficacy and reduce toxicity risk. An automated, simple, rapid, and robust LC-MS/MS analysis method was developed and validated for simultaneous quantification of plasma concentrations of 10 antibiotics and successfully applied for TDM. This method provides a shorter turnaround time compared to traditional sample batch-based analytical methods.
Therapeutic drug monitoring (TDM) of antibiotics (ATB) in patients with serious bacterial infections allows optimization of the efficacy of the treatment while reducing the risk of toxicity. Notably, early measurement of plasma beta-lactam concentration has been shown to be associated with reduced mortality in intensive care patients. In this context, a rapid, robust, and accurate assay method is essential for daily TDM.A fully automated procedure for quantification of the plasma concentrations of ten ATB was developed. The ATB were divided into two calibration pools, with Pool 1: aztreonam, ceftobiprole, cefoxitin, avibactam, tazo-bactam and Pool 2: metronidazole, ceftriaxone, daptomycin, ceftolozane, moxifloxacin. Sample preparation consisting of acetonitrile plasma protein precipitation and H20 dilution was applied to all analytes. This pro-cedure was carried out by an automated sample preparation system directly coupled to a liquid chromatography -tandem mass spectrometry (LC-MS/MS) system. Since the instrument extracts sample n while sample n-1 is in the LC-MS/MS system, the delay between obtaining the results for two samples corresponds to the analytical run time, which is less than 7 min.The method was validated according to the Food and Drug Administration guidelines. The method was sen-sitive (lower limit of quantification 0.1-1 mg/L, depending on the ATB), accurate (intra/inter-assay bias-14.8 to 14.2 %) and precise (intra/inter-assay CVs 1.27 to 16.3 %). Application of the TDM assay was illustrated by the report of an intensive care patient treated with the ceftazidime/aztreonam/avibactam combination. Four assays were performed in 8 days with results returned within 24 h to quickly manage the dose regimen in this patient.An automated, simple, rapid, robust LC-MS/MS analysis was developed and validated for the simultaneous quantification of plasma concentrations of 10 ATB and was applied with success to perform TDM. This method provides a shorter turnaround time than classic sample batch-based analytical methods.

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