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Detection of flunixin in the urine of untreated pigs housed with pigs treated with flunixin meglumine at labeled doses()

The objective of this study was to determine the likelihood that swine treated with flunixin meglumine could contaminate their environment, which could cause untreated swine housed in the same pen to ingest or absorb enough drug to be detected in their urine. Currently, any detectable level of fluni...

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Detalles Bibliográficos
Autores principales: Hairgrove, Thomas B, Mask, Joe W, Mays, Travis P, Fajt, Virginia R, Bentke, Ashley L, Warner, Jacob L, Baynes, Ronald E
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7200503/
https://www.ncbi.nlm.nih.gov/pubmed/32704903
http://dx.doi.org/10.1093/tas/txz099
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author Hairgrove, Thomas B
Mask, Joe W
Mays, Travis P
Fajt, Virginia R
Bentke, Ashley L
Warner, Jacob L
Baynes, Ronald E
author_facet Hairgrove, Thomas B
Mask, Joe W
Mays, Travis P
Fajt, Virginia R
Bentke, Ashley L
Warner, Jacob L
Baynes, Ronald E
author_sort Hairgrove, Thomas B
collection PubMed
description The objective of this study was to determine the likelihood that swine treated with flunixin meglumine could contaminate their environment, which could cause untreated swine housed in the same pen to ingest or absorb enough drug to be detected in their urine. Currently, any detectable level of flunixin found in the urine of pigs exhibited at livestock shows in Texas can disqualify the exhibitor. We conducted 2 trials in this study. The first, a pilot trial, placed pigs in 2 pens, with each pen housing a pig that did not receive a drug and a treated pig that received 2.2 mg/kg of flunixin intramuscularly. This trial demonstrated that transfer of the drug from treated to untreated pigs housed in close proximity was possible. The second trial was conducted using 10 pens, with a treated and untreated pig in each pen. Each pig receiving treatment was randomly selected and administered 2.2 mg/kg of flunixin intramuscularly; then, urine and plasma were collected from all swine for 10 d. Flunixin was detected at or above the limit of detection of 0.1 ng/mL in the urine of all treated and untreated pigs throughout the 10-d trial. Treated pigs had higher urine levels of flunixin than their untreated pen mates for 4 d post-treatment (P < 0.0001), but there was no statistical difference between pen mates during the last 5 d of the trial, making it impossible to differentiate treated from untreated pigs.
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spelling pubmed-72005032020-07-22 Detection of flunixin in the urine of untreated pigs housed with pigs treated with flunixin meglumine at labeled doses() Hairgrove, Thomas B Mask, Joe W Mays, Travis P Fajt, Virginia R Bentke, Ashley L Warner, Jacob L Baynes, Ronald E Transl Anim Sci Animal Health And Well Being The objective of this study was to determine the likelihood that swine treated with flunixin meglumine could contaminate their environment, which could cause untreated swine housed in the same pen to ingest or absorb enough drug to be detected in their urine. Currently, any detectable level of flunixin found in the urine of pigs exhibited at livestock shows in Texas can disqualify the exhibitor. We conducted 2 trials in this study. The first, a pilot trial, placed pigs in 2 pens, with each pen housing a pig that did not receive a drug and a treated pig that received 2.2 mg/kg of flunixin intramuscularly. This trial demonstrated that transfer of the drug from treated to untreated pigs housed in close proximity was possible. The second trial was conducted using 10 pens, with a treated and untreated pig in each pen. Each pig receiving treatment was randomly selected and administered 2.2 mg/kg of flunixin intramuscularly; then, urine and plasma were collected from all swine for 10 d. Flunixin was detected at or above the limit of detection of 0.1 ng/mL in the urine of all treated and untreated pigs throughout the 10-d trial. Treated pigs had higher urine levels of flunixin than their untreated pen mates for 4 d post-treatment (P < 0.0001), but there was no statistical difference between pen mates during the last 5 d of the trial, making it impossible to differentiate treated from untreated pigs. Oxford University Press 2019-06-18 /pmc/articles/PMC7200503/ /pubmed/32704903 http://dx.doi.org/10.1093/tas/txz099 Text en © The Author(s) 2019. Published by Oxford University Press on behalf of the American Society of Animal Science. http://creativecommons.org/licenses/by-nc/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/4.0/), which permits non-commercial re-use, distribution, and reproduction in any medium, provided the original work is properly cited. For commercial re-use, please contact journals.permissions@oup.com
spellingShingle Animal Health And Well Being
Hairgrove, Thomas B
Mask, Joe W
Mays, Travis P
Fajt, Virginia R
Bentke, Ashley L
Warner, Jacob L
Baynes, Ronald E
Detection of flunixin in the urine of untreated pigs housed with pigs treated with flunixin meglumine at labeled doses()
title Detection of flunixin in the urine of untreated pigs housed with pigs treated with flunixin meglumine at labeled doses()
title_full Detection of flunixin in the urine of untreated pigs housed with pigs treated with flunixin meglumine at labeled doses()
title_fullStr Detection of flunixin in the urine of untreated pigs housed with pigs treated with flunixin meglumine at labeled doses()
title_full_unstemmed Detection of flunixin in the urine of untreated pigs housed with pigs treated with flunixin meglumine at labeled doses()
title_short Detection of flunixin in the urine of untreated pigs housed with pigs treated with flunixin meglumine at labeled doses()
title_sort detection of flunixin in the urine of untreated pigs housed with pigs treated with flunixin meglumine at labeled doses()
topic Animal Health And Well Being
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7200503/
https://www.ncbi.nlm.nih.gov/pubmed/32704903
http://dx.doi.org/10.1093/tas/txz099
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