Simultaneous LC-ESI-MS/MS Quantification of Levosimendan and Its Metabolites for Therapeutic Drug Monitoring of Cardiac Surgery Patients.

LC-ESI-MS/MS OR-1855 OR-1896 cardiac surgery levosimendan metamizole metabolites therapeutic drug monitoring (TDM)

Journal

Pharmaceutics
ISSN: 1999-4923
Titre abrégé: Pharmaceutics
Pays: Switzerland
ID NLM: 101534003

Informations de publication

Date de publication:
12 Jul 2022
Historique:
received: 08 06 2022
revised: 06 07 2022
accepted: 07 07 2022
entrez: 27 7 2022
pubmed: 28 7 2022
medline: 28 7 2022
Statut: epublish

Résumé

Levosimendan is used in severe chronic cardiac insufficiency, also within the peri-operative setting. Real-life pharmacokinetic data in surgical patients is lacking, making therapeutic drug monitoring (TDM) of levosimendan, its pharmacologically active metabolite OR-1896, and its intermediate OR-1855 important. A simultaneous highly sensitive quantification of levosimendan and its metabolites in small-volume samples has not yet been described. Here, levosimendan (LLOQ 0.450 nM), OR-1896, and OR-1855 (LLOQ both 1.0 nM) were successfully quantified by LC-ESI-MS/MS after liquid-liquid extraction in 300 µL of blood. A short C8 column under reversed-phase conditions enabled simultaneous and fast quantification of levosimendan in the negative and the metabolites in the positive ionization mode in a single run within 2 min. Interestingly and unexpectedly, constitutional isomers of levosimendan metabolites with identical mass transitions and similar retention times were observed in surgical patients' samples, which we identified as the metamizole metabolites 4-aminoantipyrine and 4-acetamidoantipyrine. A longer C8 column and a modified mobile phase enabled selective quantification of all analytes in a single run within 7 min. We developed, validated, and applied highly sensitive LC-ESI-MS/MS methods for simultaneous quantification of levosimendan and its metabolites, enabling efficient TDM of cardiac surgery patients even with additional metamizole administration.

Identifiants

pubmed: 35890349
pii: pharmaceutics14071454
doi: 10.3390/pharmaceutics14071454
pmc: PMC9319272
pii:
doi:

Types de publication

Journal Article

Langues

eng

Subventions

Organisme : Stiftung Patient & klinische Pharmazie
ID : 01/2019

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Auteurs

Hannah Kipka (H)

Doctoral Program Clinical Pharmacy, University Hospital, LMU Munich, 81377 Munich, Germany.
Institute of Cardiovascular Physiology and Pathophysiology, Biomedical Center, LMU Munich, 82152 Planegg, Germany.

Roland Tomasi (R)

Department of Anaesthesiology, University Hospital, LMU Munich, 81377 Munich, Germany.

Max Hübner (M)

Department of Anaesthesiology, University Hospital, LMU Munich, 81377 Munich, Germany.
Walter Brendel Center of Experimental Medicine, LMU Munich, 81377 Munich, Germany.

Uwe Liebchen (U)

Department of Anaesthesiology, University Hospital, LMU Munich, 81377 Munich, Germany.

Christian Hagl (C)

Department of Cardiac Surgery, University Hospital, LMU Munich, 81377 Munich, Germany.
DZHK (German Centre of Cardiovascular Research), Partner Site Munich Heart Alliance, 81377 Munich, Germany.

Klaus T Wanner (KT)

Department of Pharmacy, Center for Drug Research, Ludwig-Maximilians-Universität, 81377 Munich, Germany.

Hanna Mannell (H)

Doctoral Program Clinical Pharmacy, University Hospital, LMU Munich, 81377 Munich, Germany.
Institute of Cardiovascular Physiology and Pathophysiology, Biomedical Center, LMU Munich, 82152 Planegg, Germany.

Georg Höfner (G)

Department of Pharmacy, Center for Drug Research, Ludwig-Maximilians-Universität, 81377 Munich, Germany.

Classifications MeSH