The solvent- and surface-dependent adsorption of the lipopeptide antibiotic daptomycin: The general necessity of adsorption tests.

Bioanalytics Daptomycin High performance liquid chromatography coupled to mass spectrometry Highly variable adsorption and recovery Minimal inhibitory concentration testing

Journal

Journal of pharmaceutical and biomedical analysis
ISSN: 1873-264X
Titre abrégé: J Pharm Biomed Anal
Pays: England
ID NLM: 8309336

Informations de publication

Date de publication:
25 Oct 2023
Historique:
received: 06 07 2023
revised: 15 08 2023
accepted: 16 08 2023
medline: 11 9 2023
pubmed: 25 8 2023
entrez: 24 8 2023
Statut: ppublish

Résumé

The impact of poor or non-reproducible analyte recoveries due to non-specific drug adsorption on various analytical assays is often underestimated. Even internationally approved guidelines for pharmaceutical analysis such as the EMA guideline on bioanalytical method validation, the ICH guideline M10 on bioanalytical method validation and study sample analysis or the FDA bioanalytical method validation guidance do not adequately encourage more detailed investigations. Furthermore, other areas of research in which the concentration of active pharmaceutical compounds plays a crucial role, for example screening for minimal inhibitory concentrations of bacterial isolates, are potentially affected as well. The aim of this study was to demonstrate the general necessity of drug adsorption tests, using the lipopeptide antibiotic daptomycin as an example. A wide range of typical materials used in processing samples in pharmaceutical and biological analysis, as well as various solvents and biological matrices were included in the experiments. A fully validated LC-MS/MS method was applied for the determination of daptomycin concentrations, which were subsequently used to calculate the recovery. Recovery results (n = 3) ranged from 0.00% to 102.12% with a maximum relative standard deviation of 12.78%. These findings demonstrate that recovery can vary greatly depending on the solvent and the contact material, indicating the need to be optimized and, if applicable, validated. Hence, high reproducibility can only be achieved if all materials (and their manufacturers) used in a method are specified, not just those used in steps considered critical.

Identifiants

pubmed: 37619296
pii: S0731-7085(23)00426-0
doi: 10.1016/j.jpba.2023.115657
pii:
doi:

Substances chimiques

Daptomycin NWQ5N31VKK
Anti-Bacterial Agents 0
Lipopeptides 0
Solvents 0
Pharmaceutical Preparations 0

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

115657

Informations de copyright

Copyright © 2023 Elsevier B.V. All rights reserved.

Déclaration de conflit d'intérêts

Declaration of Competing Interest The authors declare the following financial interests/personal relationships which may be considered as potential competing interests: Ulrike Holzgrabe reports financial support was provided by German Research Foundation.

Auteurs

Lukas Kirchner (L)

University of Würzburg, Institute for Pharmacy and Food Chemistry, 97074 Würzburg, Germany. Electronic address: lukas.kirchner@uni-wuerzburg.de.

Tessa Marciniak (T)

University of Würzburg, Institute for Molecular Infection Biology, 97080 Würzburg, Germany. Electronic address: tessa.marciniak@uni-wuerzburg.de.

Wilma Ziebuhr (W)

University of Würzburg, Institute for Molecular Infection Biology, 97080 Würzburg, Germany. Electronic address: wilma.ziebuhr@uni-wuerzburg.de.

Oliver Scherf-Clavel (O)

University of Würzburg, Institute for Pharmacy and Food Chemistry, 97074 Würzburg, Germany; Aalen University, Faculty of Chemistry, Beethovenstraße 1, 73430 Aalen, Germany. Electronic address: oliver.scherf-clavel@hs-aalen.de.

Ulrike Holzgrabe (U)

University of Würzburg, Institute for Pharmacy and Food Chemistry, 97074 Würzburg, Germany. Electronic address: ulrike.holzgrabe@uni-wuerzburg.de.

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Classifications MeSH