Cefepime distribution by microdialysis in peritoneal fluid of rats with or without experimental peritonitis.

Cefepime intraperitoneal infection microdialysis pharmacokinetics

Journal

APMIS : acta pathologica, microbiologica, et immunologica Scandinavica
ISSN: 1600-0463
Titre abrégé: APMIS
Pays: Denmark
ID NLM: 8803400

Informations de publication

Date de publication:
24 Apr 2024
Historique:
received: 11 12 2023
accepted: 09 04 2024
medline: 25 4 2024
pubmed: 25 4 2024
entrez: 25 4 2024
Statut: aheadofprint

Résumé

The aim of this study was to investigate the penetration of cefepime into rat peritoneal fluid by microdialysis and to determine the relationship between unbound drug plasma and tissue concentration in healthy animals and in a sepsis model established through cecal ligation and puncture-induced peritonitis. Probe recovery was performed by dialysis and retrodialysis. Cefepime was administered at a dose of 110 mg/kg intravenously. Samples were collected for about 4 h, and concentrations were determined by liquid chromatography-electrospray ionization-QTOF MS. Tissue penetration was also determined. Probe recovery in vivo was 38.78% ± 3.31% and 38.83% ± 2.74% in the control and peritonitis groups, respectively. Cefepime was rapidly distributed in the peritoneal fluid in both groups. The peritoneal fluid/plasma cefepime ratio was 0.38 and 0.32 for the control and peritonitis groups, respectively. Cefepime concentrations were above the MIC of 4 mg/L for the main enterobacteria. The infection model that was used had no apparent effect on the pharmacokinetics of cefepime in rats. This was the first study to determine free cefepime concentrations in the peritoneal fluid of healthy rats and rats with experimental peritonitis.

Identifiants

pubmed: 38659357
doi: 10.1111/apm.13418
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Informations de copyright

© 2024 Scandinavian Societies for Pathology, Medical Microbiology and Immunology.

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Auteurs

Michele Vaz Dos Anjos (MV)

Health Sciences Postgraduate Program, University of Caxias do Sul, Caxias do Sul, Brazil.

Eduarda Possa (E)

Health Sciences Postgraduate Program, University of Caxias do Sul, Caxias do Sul, Brazil.

Gisele da Silva Fonseca (GDS)

Biotechnology Postgraduate Program, University of Caxias do Sul, Caxias do Sul, Brazil.

Larissa Bergoza (L)

Health Sciences Postgraduate Program, University of Caxias do Sul, Caxias do Sul, Brazil.

Leandro Tasso (L)

Health Sciences Postgraduate Program, University of Caxias do Sul, Caxias do Sul, Brazil.
Biotechnology Postgraduate Program, University of Caxias do Sul, Caxias do Sul, Brazil.

Classifications MeSH