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Bioanalysis of six antibiotics from volumetric microsamples: a new tool for precision dosing in critically ill children

    John Takyi-Williams

    College of Pharmacy, University of Michigan, Ann Arbor, MI 48108, USA

    ,
    Abbie D Leino

    College of Pharmacy, University of Michigan, Ann Arbor, MI 48108, USA

    ,
    Ruiting Li

    College of Pharmacy, University of Michigan, Ann Arbor, MI 48108, USA

    ,
    Kevin J Downes

    Division of Infectious Diseases, Children's Hospital of Philadelphia, Philadelphia, PA 19104, USA

    ,
    Athena F Zuppa

    Division of Infectious Diseases, Children's Hospital of Philadelphia, Philadelphia, PA 19104, USA

    ,
    Amanda Bwint

    Division of Infectious Diseases, Children's Hospital of Philadelphia, Philadelphia, PA 19104, USA

    ,
    Bo Wen

    College of Pharmacy, University of Michigan, Ann Arbor, MI 48108, USA

    ,
    Duxin Sun

    College of Pharmacy, University of Michigan, Ann Arbor, MI 48108, USA

    ,
    Marc H Scheetz

    College of Pharmacy, Midwestern University, Downers Grove, IL 60515, USA

    &
    Manjunath P Pai

    *Author for correspondence:

    E-mail Address: amitpai@med.umich.edu

    College of Pharmacy, University of Michigan, Ann Arbor, MI 48108, USA

    Published Online:https://doi.org/10.4155/bio-2023-0171

    Background: Volumetric absorptive microsamples (VAMS) can support pharmacokinetic / pharmacodynamic studies. We present the bioanalytical method development for the simultaneous quantification of ampicillin, cefepime, ceftriaxone, meropenem, piperacillin, tazobactam, and vancomycin from VAMS. Methods & results: Optimal extraction, chromatographic, and mass spectrometry conditions were identified. Maximum extraction recoveries included 100 μl of water for rehydration and methanol for protein precipitation. Chromatographic separation used Phenomenex Kinetex Polar C18 column with a mobile phase comprising water/acetonitrile with formic acid and was fully validated. Hematocrit effects were only observed for vancomycin. Samples were stable for 90 days at -80°C except for meropenem, which was stable for 60 days. Conclusion: Multiple antibiotics can be assayed from a single VAMS sample to facilitate pharmacokinetic/pharmacodynamic studies.

    Papers of special note have been highlighted as: • of interest; •• of considerable interest

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