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Oral pharmacokinetics of a pharmaceutical preparation of florfenicol in broiler chickens

INTRODUCTION: The use of florfenicol must follow particular pharmacokinetic/pharmacodynamic (PK/PD) ratios, i.e., it requires achieving serum concentrations at or slightly above the pathogen's minimum inhibitory concentration (MIC) during the dosing interval and that the ratio of area under the...

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Autores principales: Gutierrez, Lilia, Guzman-Flores, Aline, Monroy-Barreto, Minerva, Ocampo, Luis, Sumano, Hector
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10284592/
https://www.ncbi.nlm.nih.gov/pubmed/37351554
http://dx.doi.org/10.3389/fvets.2023.1208221
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author Gutierrez, Lilia
Guzman-Flores, Aline
Monroy-Barreto, Minerva
Ocampo, Luis
Sumano, Hector
author_facet Gutierrez, Lilia
Guzman-Flores, Aline
Monroy-Barreto, Minerva
Ocampo, Luis
Sumano, Hector
author_sort Gutierrez, Lilia
collection PubMed
description INTRODUCTION: The use of florfenicol must follow particular pharmacokinetic/pharmacodynamic (PK/PD) ratios, i.e., it requires achieving serum concentrations at or slightly above the pathogen's minimum inhibitory concentration (MIC) during the dosing interval and that the ratio of area under the concentration vs. time curve (AUC)/MIC should be as high as possible (still undetermined for poultry). As an alternative to the standard soluble florfenicol that is administered to the flock through drinking water, florfenicol premix is often recommended as feed medication in Latin America. However, no particular pharmaceutical design has been proposed. METHODS: This study compared the PK of two preparations of florfenicol in broiler chickens and pondered the possibility of each covering the referred PK-PD ratios as predictors of clinical efficacy. The preparations comprise a pharmaceutical form as FOLA pellets (F = bioavailability; O = optimum; and LA = long-acting) and the premix formulation. The former are small colored pellets with vehicles and absorption enhancers of florfenicol designed for long action, and the latter is the reference premix of the antibiotic. First, these two pharmaceutical forms of florfenicol were administered as oral boluses (30 mg/kg), aided by a probe. In a second trial of the dosing form, both pharmaceutical preparations of florfenicol were administered in feed and ad libitum (110 ppm; ~30 mg/kg). RESULTS: In both cases, FOLA-florfenicol presented much higher relative bioavailability (3.27 times higher) and mean better residence time than florfenicol premix (two times high when forced as bolus dose). Consequently, FOLA-florfenicol possesses better PK/PD ratios than less sensitive pathogens, i.e., E. coli. It is proposed that if a metaphylactic treatment of a bacterial outbreak in poultry is implemented with florfenicol prepared as FOLA, better PK/PD ratios will be obtained than those of standard florfenicol premix. DISCUSSION: Clinicians must confirm that feed consumption in the flock has not been affected by the particular disease if FOLA pellets of florfenicol are used.
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spelling pubmed-102845922023-06-22 Oral pharmacokinetics of a pharmaceutical preparation of florfenicol in broiler chickens Gutierrez, Lilia Guzman-Flores, Aline Monroy-Barreto, Minerva Ocampo, Luis Sumano, Hector Front Vet Sci Veterinary Science INTRODUCTION: The use of florfenicol must follow particular pharmacokinetic/pharmacodynamic (PK/PD) ratios, i.e., it requires achieving serum concentrations at or slightly above the pathogen's minimum inhibitory concentration (MIC) during the dosing interval and that the ratio of area under the concentration vs. time curve (AUC)/MIC should be as high as possible (still undetermined for poultry). As an alternative to the standard soluble florfenicol that is administered to the flock through drinking water, florfenicol premix is often recommended as feed medication in Latin America. However, no particular pharmaceutical design has been proposed. METHODS: This study compared the PK of two preparations of florfenicol in broiler chickens and pondered the possibility of each covering the referred PK-PD ratios as predictors of clinical efficacy. The preparations comprise a pharmaceutical form as FOLA pellets (F = bioavailability; O = optimum; and LA = long-acting) and the premix formulation. The former are small colored pellets with vehicles and absorption enhancers of florfenicol designed for long action, and the latter is the reference premix of the antibiotic. First, these two pharmaceutical forms of florfenicol were administered as oral boluses (30 mg/kg), aided by a probe. In a second trial of the dosing form, both pharmaceutical preparations of florfenicol were administered in feed and ad libitum (110 ppm; ~30 mg/kg). RESULTS: In both cases, FOLA-florfenicol presented much higher relative bioavailability (3.27 times higher) and mean better residence time than florfenicol premix (two times high when forced as bolus dose). Consequently, FOLA-florfenicol possesses better PK/PD ratios than less sensitive pathogens, i.e., E. coli. It is proposed that if a metaphylactic treatment of a bacterial outbreak in poultry is implemented with florfenicol prepared as FOLA, better PK/PD ratios will be obtained than those of standard florfenicol premix. DISCUSSION: Clinicians must confirm that feed consumption in the flock has not been affected by the particular disease if FOLA pellets of florfenicol are used. Frontiers Media S.A. 2023-06-07 /pmc/articles/PMC10284592/ /pubmed/37351554 http://dx.doi.org/10.3389/fvets.2023.1208221 Text en Copyright © 2023 Gutierrez, Guzman-Flores, Monroy-Barreto, Ocampo and Sumano. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Veterinary Science
Gutierrez, Lilia
Guzman-Flores, Aline
Monroy-Barreto, Minerva
Ocampo, Luis
Sumano, Hector
Oral pharmacokinetics of a pharmaceutical preparation of florfenicol in broiler chickens
title Oral pharmacokinetics of a pharmaceutical preparation of florfenicol in broiler chickens
title_full Oral pharmacokinetics of a pharmaceutical preparation of florfenicol in broiler chickens
title_fullStr Oral pharmacokinetics of a pharmaceutical preparation of florfenicol in broiler chickens
title_full_unstemmed Oral pharmacokinetics of a pharmaceutical preparation of florfenicol in broiler chickens
title_short Oral pharmacokinetics of a pharmaceutical preparation of florfenicol in broiler chickens
title_sort oral pharmacokinetics of a pharmaceutical preparation of florfenicol in broiler chickens
topic Veterinary Science
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10284592/
https://www.ncbi.nlm.nih.gov/pubmed/37351554
http://dx.doi.org/10.3389/fvets.2023.1208221
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