Predicting in vivo absorption of chloramphenicol in frogs using in vitro percutaneous absorption data.


Journal

BMC veterinary research
ISSN: 1746-6148
Titre abrégé: BMC Vet Res
Pays: England
ID NLM: 101249759

Informations de publication

Date de publication:
28 Jan 2021
Historique:
received: 18 06 2020
accepted: 13 01 2021
entrez: 29 1 2021
pubmed: 30 1 2021
medline: 3 9 2021
Statut: epublish

Résumé

Infectious disease, particularly the fungal disease chytridiomycosis (caused by Batrachochytrium dendrobatidis), is a primary cause of amphibian declines and extinctions worldwide. The transdermal route, although offering a simple option for drug administration in frogs, is complicated by the lack of knowledge regarding percutaneous absorption kinetics. This study builds on our previous studies in frogs, to formulate and predict the percutaneous absorption of a drug for the treatment of infectious disease in frogs. Chloramphenicol, a drug with reported efficacy in the treatment of infectious disease including Batrachochytrium dendrobatidis, was formulated with 20% v/v propylene glycol and applied to the ventral pelvis of Rhinella marina for up to 6 h. Serum samples were taken during and up to 18 h following exposure, quantified for chloramphenicol content, and pharmacokinetic parameters were estimated using non-compartmental analysis. Serum levels of chloramphenicol reached the minimum inhibitory concentration (MIC; 12.5 μg.mL The model, based on in vitro data and adjusted for formulation components and in vivo data, was effective in predicting chloramphenicol flux to ensure the MIC for Batrachochytrium dendrobatidis was reached, with serum levels being well above the MICs for other common bacterial pathogens in frogs. Chloramphenicol's extended elimination means that a 6-h bath may be adequate to maintain serum levels for up to 24 h. We suggest trialling a reduction of the currently-recommended continuous (23 h/day for 21-35 days) chloramphenicol bathing for chytrid infection with this formulation.

Sections du résumé

BACKGROUND BACKGROUND
Infectious disease, particularly the fungal disease chytridiomycosis (caused by Batrachochytrium dendrobatidis), is a primary cause of amphibian declines and extinctions worldwide. The transdermal route, although offering a simple option for drug administration in frogs, is complicated by the lack of knowledge regarding percutaneous absorption kinetics. This study builds on our previous studies in frogs, to formulate and predict the percutaneous absorption of a drug for the treatment of infectious disease in frogs. Chloramphenicol, a drug with reported efficacy in the treatment of infectious disease including Batrachochytrium dendrobatidis, was formulated with 20% v/v propylene glycol and applied to the ventral pelvis of Rhinella marina for up to 6 h. Serum samples were taken during and up to 18 h following exposure, quantified for chloramphenicol content, and pharmacokinetic parameters were estimated using non-compartmental analysis.
RESULTS RESULTS
Serum levels of chloramphenicol reached the minimum inhibitory concentration (MIC; 12.5 μg.mL
CONCLUSIONS CONCLUSIONS
The model, based on in vitro data and adjusted for formulation components and in vivo data, was effective in predicting chloramphenicol flux to ensure the MIC for Batrachochytrium dendrobatidis was reached, with serum levels being well above the MICs for other common bacterial pathogens in frogs. Chloramphenicol's extended elimination means that a 6-h bath may be adequate to maintain serum levels for up to 24 h. We suggest trialling a reduction of the currently-recommended continuous (23 h/day for 21-35 days) chloramphenicol bathing for chytrid infection with this formulation.

Identifiants

pubmed: 33509166
doi: 10.1186/s12917-021-02765-5
pii: 10.1186/s12917-021-02765-5
pmc: PMC7842057
doi:

Substances chimiques

Anti-Bacterial Agents 0
Chloramphenicol 66974FR9Q1

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

57

Commentaires et corrections

Type : ErratumIn

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Auteurs

Victoria K Llewelyn (VK)

Pharmacy, College of Medicine and Dentistry, James Cook University, Townsville, Australia. victoria.llewelyn@my.jcu.edu.au.
College of Nursing and Health Sciences, Flinders University, Adelaide, Australia. victoria.llewelyn@my.jcu.edu.au.

Lee Berger (L)

One Health Research Group, Melbourne Veterinary School, University of Melbourne, Werribee, Australia.

Beverley D Glass (BD)

Pharmacy, College of Medicine and Dentistry, James Cook University, Townsville, Australia.

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