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Simultaneous Measurement of 11 Antibiotics for use in the Intensive Care Unit by Ultra Performance Liquid Chromatography-Tandem Mass Spectrometry
Department of Clinical Microbiology, Kalmar County Hospital, Kalmar, Sweden; Department of Medicine and Optometry, Linnaeus University, Kalmar, Sweden.
Linköping University, Department of Biomedical and Clinical Sciences, Division of Clinical Chemistry and Pharmacology. Linköping University, Faculty of Medicine and Health Sciences. Region Östergötland, Center for Diagnostics, Department of Clinical Pharmacology.
Linköping University, Department of Biomedical and Clinical Sciences, Division of Clinical Chemistry and Pharmacology. Linköping University, Faculty of Medicine and Health Sciences. Region Östergötland, Center for Diagnostics, Department of Clinical Pharmacology.
Linköping University, Department of Biomedical and Clinical Sciences, Division of Inflammation and Infection. Linköping University, Faculty of Medicine and Health Sciences. Region Östergötland, Medicine Center, Department of Infectious Diseases.ORCID iD: 0000-0002-0854-7508
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2022 (English)In: Therapeutic Drug Monitoring, ISSN 0163-4356, E-ISSN 1536-3694, Vol. 44, no 2, p. 308-318Article in journal (Refereed) Published
Abstract [en]

BACKGROUND: Recent studies indicate that a high proportion of patients in the intensive care unit (ICU) fail to attain adequate antibiotic levels. Thus, there is a need to monitor the antibiotic concentration to ensure effective treatment. Herein, the authors aimed to develop an ultra-high performance liquid chromatography-tandem mass spectrometry (UHPLC-MS/MS) method for the simultaneous quantification of antimicrobials to assess individualized therapeutic drug monitoring (TDM).

METHODS: A UHPLC-MS/MS method with 11 antibiotics (ciprofloxacin, moxifloxacin, benzylpenicillin, levofloxacin, linezolid, rifampicin, meropenem, cloxacillin, cefotaxime, clindamycin, and piperacillin) was developed. Chromatographic separation was performed using a Kinetex biphenyl reversed-phase column, with gradient elution using 0.1% formic acid (FA) and methanol with 0.1% FA. Sample preparation was performed using methanol protein precipitation. The total run time was 5 min.

RESULTS: For all analytes, the inter-assay inaccuracies for calibrators were ≤5%. The inter-day inaccuracies for the quality controls (QCs) were ≤5% for all analytes. The inter-assay precision for calibration standards ranged between 1.42% and 6.11%. The inter-assay imprecision for QCs of all antibiotics and concentrations ranged between 3.60% and 16.1%. Inter-assay inaccuracy and imprecision for the QCs and calibration standards were ≤15% for all drugs, except benzylpenicillin.

CONCLUSION: A rapid UHPLC-MS/MS method was developed for the simultaneous quantification of 11 different antibiotics. Minimal sample preparation was required to ensure a rapid turnaround time. The method was applied to clinical samples collected from four ICUs.

Place, publisher, year, edition, pages
Philadelphia, PA, United States: Lippincott Williams & Wilkins, 2022. Vol. 44, no 2, p. 308-318
Keywords [en]
UHPLC-MS/MS; Antibiotics; Therapeutic drug monitoring; Critically ill patients; Clinical application
National Category
Analytical Chemistry
Identifiers
URN: urn:nbn:se:liu:diva-183609DOI: 10.1097/ftd.0000000000000911ISI: 000769195300007PubMedID: 34224537OAI: oai:DiVA.org:liu-183609DiVA, id: diva2:1644459
Note

Funding: Research Council of South-East Sweden (FORSS); Swedish Research CouncilSwedish Research CouncilEuropean Commission; Marianne and Marcus Wallenberg Foundation [DNR 2014/236-31]

Available from: 2022-03-14 Created: 2022-03-14 Last updated: 2024-05-05Bibliographically approved

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Karlsson, LouiseHällgren, AnitaSchön, ThomasCarlsson, Björn

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Karlsson, LouiseÄrlemalm, AndreasHällgren, AnitaSchön, ThomasCarlsson, Björn
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Division of Clinical Chemistry and PharmacologyFaculty of Medicine and Health SciencesDepartment of Clinical PharmacologyDivision of Inflammation and InfectionDepartment of Infectious Diseases
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Therapeutic Drug Monitoring
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