Dosage assessment of valnemulin in pigs based on population pharmacokinetic and Monte Carlo simulation |
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Authors: | Y. X. Zhang J. Sun X. Y. Luo L. X. Zhu Z. Zhang R. Wang Y. H. Liu |
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Affiliation: | 1. College of Veterinary Medicine, South China Agricultural University, Guangzhou, Guangdong Province, China;2. Guangdong Provincial Key Laboratory of Prevention and Control for Severe Clinical Animal Diseases, Guangzhou, Guangdong Province, China |
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Abstract: | ![]() To estimate the valnemulin pharmacokinetic profile in a swine population and to assess a dosage regimen for increasing the likelihood of optimization. This study was, respectively, performed in 22 sows culled by p.o. administration and in 80 growing‐finishing pigs by i.v. administration at a single dose of 10 mg/kg to develop a population pharmacokinetic model and Monte Carlo simulation. The relationships among the plasma concentration, dose, and time of valnemulin in pigs were illustrated as Ci,v = X0(8.4191 × 10‐4 × e?0.2371t + 1.2788 × 10?5 × e?0.0069t) after i.v. and Cp.o = X0(?8.4964 × 10?4 × e?0.5840t + 8.4195 × e?0.2371t + 7.6869 × 10?6 × e?0.0069t) after p.o. Monte Carlo simulation showed that T>MIC was more than 24 h when a single daily dosage at 13.5 mg/kg BW in pigs was administrated by p.o., and MIC was 0.031 mg/L. It was concluded that the current dosage regimen at 10–12 mg/kg BW led to valnemulin underexposure if the MIC was more than 0.031 mg/L and could increase the risk of treatment failure and/or drug resistance. |
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