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Food Addit Contam Part A Chem Anal Control Expo Risk Assess. 2015;32(12):2002-17. doi: 10.1080/19440049.2015.1100330. Epub 2015 Nov 5.

Estimation of residue depletion of cyadox and its marker residue in edible tissues of pigs using physiologically based pharmacokinetic modelling.

Author information

1
a MOA Laboratory of Risk Assessment for Quality and Safety of Livestock and Poultry Products, Huazhong Agricultural University , Wuhan , 430070 , China.
2
b Institute of Computational Comparative Medicine (ICCM), College of Veterinary Medicine , Kansas State University , Manhattan , KS 66506 , USA.
3
c Hubei Collaborative Innovation Center for Animal Nutrition and Feed Safety , Huazhong Agricultural University , Wuhan , 430070 , China.
4
d National Reference Laboratory of Veterinary Drug Residues (HZAU) and MAO Key Laboratory for Detection of Veterinary Drug Residues, Huazhong Agricultural University , Wuhan , 430070 , China.

Abstract

Physiologically based pharmacokinetic (PBPK) models are powerful tools to predict tissue distribution and depletion of veterinary drugs in food animals. However, most models only simulate the pharmacokinetics of the parent drug without considering their metabolites. In this study, a PBPK model was developed to simultaneously describe the depletion in pigs of the food animal antimicrobial agent cyadox (CYA), and its marker residue 1,4-bisdesoxycyadox (BDCYA). The CYA and BDCYA sub-models included blood, liver, kidney, gastrointestinal tract, muscle, fat and other organ compartments. Extent of plasma-protein binding, renal clearance and tissue-plasma partition coefficients of BDCYA were measured experimentally. The model was calibrated with the reported pharmacokinetic and residue depletion data from pigs dosed by oral gavage with CYA for five consecutive days, and then extrapolated to exposure in feed for two months. The model was validated with 14 consecutive day feed administration data. This PBPK model accurately simulated CYA and BDCYA in four edible tissues at 24-120 h after both oral exposure and 2-month feed administration. There was only slight overestimation of CYA in muscle and BDCYA in kidney at earlier time points (6-12 h) when dosed in feed. Monte Carlo analysis revealed excellent agreement between the estimated concentration distributions and observed data. The present model could be used for tissue residue monitoring of CYA and BDCYA in food animals, and provides a foundation for developing PBPK models to predict residue depletion of both parent drugs and their metabolites in food animals.

KEYWORDS:

1,4-bisdesoxycyadox; Monte Carlo analysis; PBPK modelling; cyadox; residue prediction; sensitivity analysis; tissue depletion

PMID:
26414219
DOI:
10.1080/19440049.2015.1100330
[Indexed for MEDLINE]

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