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Systemic and mammary gland disposition of enrofloxacin in healthy sheep following intramammary administration

BACKGROUND: Mastitis is one of the most important diseases affecting dairy sheep. Antimicrobial drugs are often administered directly through teat to treat or prevent this disease, but data on drug distribution within glandular tissue are scarce and it cannot be estimated from concentrations in milk...

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Autores principales: López, Cristina, García, Juan José, Sierra, Matilde, Diez, María José, Pérez, Claudia, Sahagún, Ana Maria, Fernández, Nélida
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4396189/
https://www.ncbi.nlm.nih.gov/pubmed/25889369
http://dx.doi.org/10.1186/s12917-015-0406-9
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author López, Cristina
García, Juan José
Sierra, Matilde
Diez, María José
Pérez, Claudia
Sahagún, Ana Maria
Fernández, Nélida
author_facet López, Cristina
García, Juan José
Sierra, Matilde
Diez, María José
Pérez, Claudia
Sahagún, Ana Maria
Fernández, Nélida
author_sort López, Cristina
collection PubMed
description BACKGROUND: Mastitis is one of the most important diseases affecting dairy sheep. Antimicrobial drugs are often administered directly through teat to treat or prevent this disease, but data on drug distribution within glandular tissue are scarce and it cannot be estimated from concentrations in milk. Thus, the aim of this study was to investigate systemic and mammary gland distribution of enrofloxacin after intramammary administration. The drug was administered to 6 healthy lactating Assaf sheep with an injector containing an enrofloxacin preparation (1 g drug/5 g ointment). Blood samples were collected at 0, 30, 60, 90, 120, 150 and 180 min. Animals were then sedated and sacrificed, and glandular tissue samples were obtained from treated udders at 2, 4, 6 and 8 cm height. Enrofloxacin concentrations were measured in plasma and tissue samples by UV high-performed liquid chromatography. RESULTS: Mean enrofloxacin plasma concentrations were below 0.5 μg/mL. Mean tissue concentrations decreased in mammary gland with vertical distance from the teat, ranging from 356.6 μg/g at 2 cm to 95.60 μg/g at the base of the udder. Glandular tissue concentrations best fitted to a decreasing monoexponential model, and showed a good correlation with an ex vivo model previously developed. CONCLUSIONS: Enrofloxacin concentrations were effective in the entire glandular tissue against the main pathogens causing mastitis in sheep. These results suggest that this drug may be suitable to treat mastitis in sheep by intramammary administration.
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spelling pubmed-43961892015-04-15 Systemic and mammary gland disposition of enrofloxacin in healthy sheep following intramammary administration López, Cristina García, Juan José Sierra, Matilde Diez, María José Pérez, Claudia Sahagún, Ana Maria Fernández, Nélida BMC Vet Res Research Article BACKGROUND: Mastitis is one of the most important diseases affecting dairy sheep. Antimicrobial drugs are often administered directly through teat to treat or prevent this disease, but data on drug distribution within glandular tissue are scarce and it cannot be estimated from concentrations in milk. Thus, the aim of this study was to investigate systemic and mammary gland distribution of enrofloxacin after intramammary administration. The drug was administered to 6 healthy lactating Assaf sheep with an injector containing an enrofloxacin preparation (1 g drug/5 g ointment). Blood samples were collected at 0, 30, 60, 90, 120, 150 and 180 min. Animals were then sedated and sacrificed, and glandular tissue samples were obtained from treated udders at 2, 4, 6 and 8 cm height. Enrofloxacin concentrations were measured in plasma and tissue samples by UV high-performed liquid chromatography. RESULTS: Mean enrofloxacin plasma concentrations were below 0.5 μg/mL. Mean tissue concentrations decreased in mammary gland with vertical distance from the teat, ranging from 356.6 μg/g at 2 cm to 95.60 μg/g at the base of the udder. Glandular tissue concentrations best fitted to a decreasing monoexponential model, and showed a good correlation with an ex vivo model previously developed. CONCLUSIONS: Enrofloxacin concentrations were effective in the entire glandular tissue against the main pathogens causing mastitis in sheep. These results suggest that this drug may be suitable to treat mastitis in sheep by intramammary administration. BioMed Central 2015-04-09 /pmc/articles/PMC4396189/ /pubmed/25889369 http://dx.doi.org/10.1186/s12917-015-0406-9 Text en © Lopez et al.; licensee BioMed Central. 2015 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly credited. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Research Article
López, Cristina
García, Juan José
Sierra, Matilde
Diez, María José
Pérez, Claudia
Sahagún, Ana Maria
Fernández, Nélida
Systemic and mammary gland disposition of enrofloxacin in healthy sheep following intramammary administration
title Systemic and mammary gland disposition of enrofloxacin in healthy sheep following intramammary administration
title_full Systemic and mammary gland disposition of enrofloxacin in healthy sheep following intramammary administration
title_fullStr Systemic and mammary gland disposition of enrofloxacin in healthy sheep following intramammary administration
title_full_unstemmed Systemic and mammary gland disposition of enrofloxacin in healthy sheep following intramammary administration
title_short Systemic and mammary gland disposition of enrofloxacin in healthy sheep following intramammary administration
title_sort systemic and mammary gland disposition of enrofloxacin in healthy sheep following intramammary administration
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4396189/
https://www.ncbi.nlm.nih.gov/pubmed/25889369
http://dx.doi.org/10.1186/s12917-015-0406-9
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