Evaluation of Benzylpenicillin as an Internal Standard for Measurement of Piperacillin Bone Concentrations Via Microdialysis.

Antiinfective(s) HPLC Microdialysis Pharmacokinetics Piperacillin Tissue concentrations

Journal

Journal of pharmaceutical sciences
ISSN: 1520-6017
Titre abrégé: J Pharm Sci
Pays: United States
ID NLM: 2985195R

Informations de publication

Date de publication:
10 2021
Historique:
received: 12 02 2021
revised: 03 06 2021
accepted: 03 06 2021
pubmed: 9 6 2021
medline: 25 2 2023
entrez: 8 6 2021
Statut: ppublish

Résumé

Microdialysis is a pharmacokinetic tool that can be advantageous when obtaining tissues' pharmacokinetic information. Since absolute extracellular tissue concentrations are needed in pharmacokinetic studies, calibrating the microdialysis system is necessary. The internal standard method is superior when compared to other calibration methods. However, thorough evaluation of the internal standard is required before it can be used. In vitro experiments and an in vivo study on pigs (n = 8) were conducted to assess the relative recoveries by gain and by loss for piperacillin, both with and without a benzylpenicillin concentration of 5 µg/mL. Furthermore, the in vivo setup allowed for an evaluation of piperacillin cancellous bone and subcutaneous tissue concentrations in a single 8 h dosing interval. Ultra-high performance liquid chromatography (UHPLC) was used to determine piperacillin and benzylpenicillin concentrations. Relative recovery by loss for benzylpenicillin and relative recovery by gain for piperacillin were similar in in vitro and in vivo. Presence of benzylpenicillin did not affect the relative recovery for piperacillin. Relative recovery, pharmacokinetic parameters and fT>MIC were similar when comparing the retrodialysis by drug and the internal standard calibration methods (p > 0.31). Mean fT>MIC (16 µg/mL) for plasma, cancellous bone and subcutaneous tissue were 232 min, 255 min and 295 min, respectively. Our findings suggest that benzylpenicillin is suitable as an internal standard for piperacillin in microdialysis studies. Mean fT>MIC (16 µg/mL) for plasma, cancellous bone, and subcutaneous tissue reached a target of 50% fT>MIC under the investigated conditions (mean range: 52%-66%); however, the target was not obtained in all pigs in all compartments. Moreover, 100% fT>MIC was not obtained in any case, suggesting that different strategies must be taken into consideration if higher targets are employed.

Identifiants

pubmed: 34102200
pii: S0022-3549(21)00298-7
doi: 10.1016/j.xphs.2021.06.008
pii:
doi:

Substances chimiques

Anti-Bacterial Agents 0
Piperacillin X00B0D5O0E

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

3500-3506

Informations de copyright

Copyright © 2021 The Authors. Published by Elsevier Inc. All rights reserved.

Déclaration de conflit d'intérêts

Declaration of Competing Interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper.

Auteurs

Martin Knudsen (M)

Department of Clinical Medicine, Aarhus University, Denmark; Aarhus Microdialysis Research Group, Aarhus University Hospital, Palle Juul-Jensens Boulevard 165, Crossing J112, 8200 Aarhus N, Denmark. Electronic address: martinknudsen@clin.au.dk.

Mats Bue (M)

Department of Clinical Medicine, Aarhus University, Denmark; Aarhus Microdialysis Research Group, Aarhus University Hospital, Palle Juul-Jensens Boulevard 165, Crossing J112, 8200 Aarhus N, Denmark; Department of Orthopedic Surgery, Aarhus University Hospital, Denmark.

Louise L Pontoppidan (LL)

Department of Surgery, Lillebaelt Hospital Kolding, Denmark.

Magnus A Hvistendahl (MA)

Department of Clinical Medicine, Aarhus University, Denmark; Aarhus Microdialysis Research Group, Aarhus University Hospital, Palle Juul-Jensens Boulevard 165, Crossing J112, 8200 Aarhus N, Denmark.

Kjeld Søballe (K)

Department of Clinical Medicine, Aarhus University, Denmark; Department of Orthopedic Surgery, Aarhus University Hospital, Denmark.

Maiken Stilling (M)

Department of Clinical Medicine, Aarhus University, Denmark; Aarhus Microdialysis Research Group, Aarhus University Hospital, Palle Juul-Jensens Boulevard 165, Crossing J112, 8200 Aarhus N, Denmark; Department of Orthopedic Surgery, Aarhus University Hospital, Denmark.

Pelle Hanberg (P)

Department of Clinical Medicine, Aarhus University, Denmark; Aarhus Microdialysis Research Group, Aarhus University Hospital, Palle Juul-Jensens Boulevard 165, Crossing J112, 8200 Aarhus N, Denmark; Department of Orthopedic Surgery, Horsens Regional Hospital, Denmark.

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Classifications MeSH