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In vivo antimicrobial activity of marbofloxacin against Pasteurella multocida in a tissue cage model in calves
Marbofloxacin is a fluoroquinolone specially developed for use in veterinary medicine with broad-spectrum antibacterial activity. The objective of our study was to re-evaluate in vivo antimicrobial activity of marbofloxacin against Pasteurella multocida using subcutaneously implanted tissue cages in...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Frontiers Media S.A.
2015
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4513234/ https://www.ncbi.nlm.nih.gov/pubmed/26257726 http://dx.doi.org/10.3389/fmicb.2015.00759 |
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author | Cao, Changfu Qu, Ying Sun, Meizhen Qiu, Zhenzhen Huang, Xianhui Huai, Binbin Lu, Yan Zeng, Zhenling |
author_facet | Cao, Changfu Qu, Ying Sun, Meizhen Qiu, Zhenzhen Huang, Xianhui Huai, Binbin Lu, Yan Zeng, Zhenling |
author_sort | Cao, Changfu |
collection | PubMed |
description | Marbofloxacin is a fluoroquinolone specially developed for use in veterinary medicine with broad-spectrum antibacterial activity. The objective of our study was to re-evaluate in vivo antimicrobial activity of marbofloxacin against Pasteurella multocida using subcutaneously implanted tissue cages in calves. Calves were infected by direct injection into tissue cages with P. multocida(type B, serotype 2), then intramuscularly received a range of marbofloxacin doses 24 h after inoculation. The ratio of 24 h area under the concentration-time curve divided by the minimum inhibitory concentration or the mutant prevention concentration (AUC(24) (h)/MIC or AUC(24) (h)/MPC) was the pharmacokinetic-pharmacodynamic (PK/PD) index that best described the effectiveness of marbofloxacin against P. multocida (R(2) = 0.8514) by non-linear regression analysis. Marbofloxacin exhibited a good antimicrobial activity in vivo. The levels of AUC(24) (h)/MIC and AUC(24) (h)/MPC that produced 50% (1.5log(10) CFU/mL reduction) and 90% (3log(10) CFU/mL reduction) of maximum response were 18.60 and 50.65 h, 4.67 and 12.89 h by using sigmoid E(max) model WINNONLIN software, respectively. The in vivo PK/PD integrated methods by tissue cage model display the advantage of the evaluation of antimicrobial activity and the optimization of the dosage regimen for antibiotics in the presence of the host defenses, especially in target animal of veterinary interest. |
format | Online Article Text |
id | pubmed-4513234 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-45132342015-08-07 In vivo antimicrobial activity of marbofloxacin against Pasteurella multocida in a tissue cage model in calves Cao, Changfu Qu, Ying Sun, Meizhen Qiu, Zhenzhen Huang, Xianhui Huai, Binbin Lu, Yan Zeng, Zhenling Front Microbiol Microbiology Marbofloxacin is a fluoroquinolone specially developed for use in veterinary medicine with broad-spectrum antibacterial activity. The objective of our study was to re-evaluate in vivo antimicrobial activity of marbofloxacin against Pasteurella multocida using subcutaneously implanted tissue cages in calves. Calves were infected by direct injection into tissue cages with P. multocida(type B, serotype 2), then intramuscularly received a range of marbofloxacin doses 24 h after inoculation. The ratio of 24 h area under the concentration-time curve divided by the minimum inhibitory concentration or the mutant prevention concentration (AUC(24) (h)/MIC or AUC(24) (h)/MPC) was the pharmacokinetic-pharmacodynamic (PK/PD) index that best described the effectiveness of marbofloxacin against P. multocida (R(2) = 0.8514) by non-linear regression analysis. Marbofloxacin exhibited a good antimicrobial activity in vivo. The levels of AUC(24) (h)/MIC and AUC(24) (h)/MPC that produced 50% (1.5log(10) CFU/mL reduction) and 90% (3log(10) CFU/mL reduction) of maximum response were 18.60 and 50.65 h, 4.67 and 12.89 h by using sigmoid E(max) model WINNONLIN software, respectively. The in vivo PK/PD integrated methods by tissue cage model display the advantage of the evaluation of antimicrobial activity and the optimization of the dosage regimen for antibiotics in the presence of the host defenses, especially in target animal of veterinary interest. Frontiers Media S.A. 2015-07-24 /pmc/articles/PMC4513234/ /pubmed/26257726 http://dx.doi.org/10.3389/fmicb.2015.00759 Text en Copyright © 2015 Cao, Qu, Sun, Qiu, Huang, Huai, Lu and Zeng. http://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) or licensor 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 | Microbiology Cao, Changfu Qu, Ying Sun, Meizhen Qiu, Zhenzhen Huang, Xianhui Huai, Binbin Lu, Yan Zeng, Zhenling In vivo antimicrobial activity of marbofloxacin against Pasteurella multocida in a tissue cage model in calves |
title | In vivo antimicrobial activity of marbofloxacin against Pasteurella multocida in a tissue cage model in calves |
title_full | In vivo antimicrobial activity of marbofloxacin against Pasteurella multocida in a tissue cage model in calves |
title_fullStr | In vivo antimicrobial activity of marbofloxacin against Pasteurella multocida in a tissue cage model in calves |
title_full_unstemmed | In vivo antimicrobial activity of marbofloxacin against Pasteurella multocida in a tissue cage model in calves |
title_short | In vivo antimicrobial activity of marbofloxacin against Pasteurella multocida in a tissue cage model in calves |
title_sort | in vivo antimicrobial activity of marbofloxacin against pasteurella multocida in a tissue cage model in calves |
topic | Microbiology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4513234/ https://www.ncbi.nlm.nih.gov/pubmed/26257726 http://dx.doi.org/10.3389/fmicb.2015.00759 |
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