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Pharmacokinetic and Pharmacodynamic Evaluation of Marbofloxacin and PK/PD Modeling against Escherichia coli in Pigs

The aim of this study was to evaluate the activity of marbofloxacin and establish the optimal dose regimens for decreasing the development of fluoroquinolone resistance in pigs against Escherichia coli with ex vivo pharmacokinetic/pharmacodynamic (PK/PD) modeling. The recommended dose (2 mg/kg body...

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Autores principales: Lei, Zhixin, Liu, Qianying, Xiong, Jincheng, Yang, Bing, Yang, Shuaike, Zhu, Qianqian, Li, Kun, Zhang, Shishuo, Cao, Jiyue, He, Qigai
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5566571/
https://www.ncbi.nlm.nih.gov/pubmed/28871226
http://dx.doi.org/10.3389/fphar.2017.00542
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author Lei, Zhixin
Liu, Qianying
Xiong, Jincheng
Yang, Bing
Yang, Shuaike
Zhu, Qianqian
Li, Kun
Zhang, Shishuo
Cao, Jiyue
He, Qigai
author_facet Lei, Zhixin
Liu, Qianying
Xiong, Jincheng
Yang, Bing
Yang, Shuaike
Zhu, Qianqian
Li, Kun
Zhang, Shishuo
Cao, Jiyue
He, Qigai
author_sort Lei, Zhixin
collection PubMed
description The aim of this study was to evaluate the activity of marbofloxacin and establish the optimal dose regimens for decreasing the development of fluoroquinolone resistance in pigs against Escherichia coli with ex vivo pharmacokinetic/pharmacodynamic (PK/PD) modeling. The recommended dose (2 mg/kg body weight) of marbofloxacin was orally administered in healthy pigs. The ileum content and plasma were both collected for the determination of marbofloxacin. The main parameters of C(max), AUC(0-24 h), AUC, Ke, t(1/2ke), MRT and Cl(b) were 11.28 μg/g, 46.15, 77.81 μg⋅h/g, 0.001 h(-1), 69.97 h, 52.45 h, 0.026 kg/h in ileum content, and 0.55 μg/ml, 8.15, 14.67 μg⋅h/ml, 0.023 h(-1), 30.67 h, 34.83 h, 0.14 L/h in plasma, respectively In total, 218 E. coli strains were isolated from most cities of China. The antibacterial activity in vitro and ex vivo of marbofloxacin against E. coli was determined following CLSI guidance. The MIC(90) of sensitive strains (142) was calculated as 2 μg/ml. The minimum inhibitory concentration (MIC) of HB197 was 2 and 4 μg/ml in broth and ileum fluids, respectively. In vitro mutant prevention concentration, growth and killing-time in vitro and ex vivo of marbofloxacin against selected HB197 were assayed for pharmacodynamic studies. According to the inhibitory sigmoid E(max) modeling, the value of AUC(0-24 h)/MIC produced in ileum content was achieved, and bacteriostatic, bactericidal activity, and elimination were calculated as 16.26, 23.54, and 27.18 h, respectively. Based on Monte Carlo simulations to obtain 90% target attainment rate, the optimal doses to achieve bacteriostatic, bactericidal, and elimination effects were 0.85, 1.22, and 1.41 mg/kg.bw for 50% target, respectively, and 0.92, 1.33, and 1.53 mg/kg.bw for 90% target, respectively, after oral administration. The results in this study provided a more optimized alternative for clinical use and demonstrated that the dosage 2 mg/kg of marbofloxacin by oral administration could have an effect on bactericidal activity against E. coli.
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spelling pubmed-55665712017-09-04 Pharmacokinetic and Pharmacodynamic Evaluation of Marbofloxacin and PK/PD Modeling against Escherichia coli in Pigs Lei, Zhixin Liu, Qianying Xiong, Jincheng Yang, Bing Yang, Shuaike Zhu, Qianqian Li, Kun Zhang, Shishuo Cao, Jiyue He, Qigai Front Pharmacol Pharmacology The aim of this study was to evaluate the activity of marbofloxacin and establish the optimal dose regimens for decreasing the development of fluoroquinolone resistance in pigs against Escherichia coli with ex vivo pharmacokinetic/pharmacodynamic (PK/PD) modeling. The recommended dose (2 mg/kg body weight) of marbofloxacin was orally administered in healthy pigs. The ileum content and plasma were both collected for the determination of marbofloxacin. The main parameters of C(max), AUC(0-24 h), AUC, Ke, t(1/2ke), MRT and Cl(b) were 11.28 μg/g, 46.15, 77.81 μg⋅h/g, 0.001 h(-1), 69.97 h, 52.45 h, 0.026 kg/h in ileum content, and 0.55 μg/ml, 8.15, 14.67 μg⋅h/ml, 0.023 h(-1), 30.67 h, 34.83 h, 0.14 L/h in plasma, respectively In total, 218 E. coli strains were isolated from most cities of China. The antibacterial activity in vitro and ex vivo of marbofloxacin against E. coli was determined following CLSI guidance. The MIC(90) of sensitive strains (142) was calculated as 2 μg/ml. The minimum inhibitory concentration (MIC) of HB197 was 2 and 4 μg/ml in broth and ileum fluids, respectively. In vitro mutant prevention concentration, growth and killing-time in vitro and ex vivo of marbofloxacin against selected HB197 were assayed for pharmacodynamic studies. According to the inhibitory sigmoid E(max) modeling, the value of AUC(0-24 h)/MIC produced in ileum content was achieved, and bacteriostatic, bactericidal activity, and elimination were calculated as 16.26, 23.54, and 27.18 h, respectively. Based on Monte Carlo simulations to obtain 90% target attainment rate, the optimal doses to achieve bacteriostatic, bactericidal, and elimination effects were 0.85, 1.22, and 1.41 mg/kg.bw for 50% target, respectively, and 0.92, 1.33, and 1.53 mg/kg.bw for 90% target, respectively, after oral administration. The results in this study provided a more optimized alternative for clinical use and demonstrated that the dosage 2 mg/kg of marbofloxacin by oral administration could have an effect on bactericidal activity against E. coli. Frontiers Media S.A. 2017-08-21 /pmc/articles/PMC5566571/ /pubmed/28871226 http://dx.doi.org/10.3389/fphar.2017.00542 Text en Copyright © 2017 Lei, Liu, Xiong, Yang, Yang, Zhu, Li, Zhang, Cao and He. 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 Pharmacology
Lei, Zhixin
Liu, Qianying
Xiong, Jincheng
Yang, Bing
Yang, Shuaike
Zhu, Qianqian
Li, Kun
Zhang, Shishuo
Cao, Jiyue
He, Qigai
Pharmacokinetic and Pharmacodynamic Evaluation of Marbofloxacin and PK/PD Modeling against Escherichia coli in Pigs
title Pharmacokinetic and Pharmacodynamic Evaluation of Marbofloxacin and PK/PD Modeling against Escherichia coli in Pigs
title_full Pharmacokinetic and Pharmacodynamic Evaluation of Marbofloxacin and PK/PD Modeling against Escherichia coli in Pigs
title_fullStr Pharmacokinetic and Pharmacodynamic Evaluation of Marbofloxacin and PK/PD Modeling against Escherichia coli in Pigs
title_full_unstemmed Pharmacokinetic and Pharmacodynamic Evaluation of Marbofloxacin and PK/PD Modeling against Escherichia coli in Pigs
title_short Pharmacokinetic and Pharmacodynamic Evaluation of Marbofloxacin and PK/PD Modeling against Escherichia coli in Pigs
title_sort pharmacokinetic and pharmacodynamic evaluation of marbofloxacin and pk/pd modeling against escherichia coli in pigs
topic Pharmacology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5566571/
https://www.ncbi.nlm.nih.gov/pubmed/28871226
http://dx.doi.org/10.3389/fphar.2017.00542
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