Estimating meat withdrawal times in pigs exposed to melamine contaminated feed using a physiologically based pharmacokinetic model

被引:92
作者
Buur, Jennifer L. [1 ]
Baynes, Ronald E. [1 ]
Riviere, Jim E. [1 ]
机构
[1] N Carolina State Univ, Coll Vet Med, Ctr Chem Toxicol Res & Pharmacokinet, Food Anim Residue Avoidance Databank, Raleigh, NC 27606 USA
关键词
PBPK; melamine; rat; porcine; meat withdrawal time; feed contaminants;
D O I
10.1016/j.yrtph.2008.05.003
中图分类号
DF [法律]; D9 [法律]; R [医药、卫生];
学科分类号
0301 ; 10 ;
摘要
Recently melamine was found to have contaminated the feed of multiple food production species leading to concern over the ability to establish an appropriate withdrawal interval and protect the safety of the food supply. To establish an appropriate withdrawal interval, a physiologically based pharmacokinetic (PBPK) model for melamine was developed for rats and extrapolated to pigs. The rat model underpredicted plasma concentrations, but better predicted tissue residues. Correlation values for plasma, kidney, and liver were 0.59, 0.76, and 0.73, respectively. The pig model underpredicted early plasma time points but had greater accuracy at later time points which is relevant to withdrawal times. Correlation (R-2) between predicted and observed plasma values was 0.89 with a negative intercept of -0.76. The pig model estimated a withdrawal interval (based on kidney tissue residues) of 19.2 and 20.9 h for single oral exposures of 3.0 and 5.12 mg/kg of melamine, respectively. Chronic oral dosing (3.0 and 5.12 mg/kg twice daily for 7 days) yielded withdrawal intervals of 20 and 21.3 h, respectively. PBPK models, such as this one, provide evidence of the usefulness in species extrapolation over a range of dosing scenarios and can be used to protect the food supply after accidental exposure in the face of little in the target species. (c) 2008 Elsevier Inc. All rights reserved.
引用
收藏
页码:324 / 331
页数:8
相关论文
共 30 条
[11]   Application of a physiologically based pharmacokinetic model for reference dose and reference concentration estimation for acetone [J].
Gentry, PR ;
Covington, TR ;
Clewell, H ;
Anderson, ME .
JOURNAL OF TOXICOLOGY AND ENVIRONMENTAL HEALTH-PART A-CURRENT ISSUES, 2003, 66 (23) :2209-2225
[12]   Physiologically-based pharmacokinetic simulation modelling [J].
Grass, GM ;
Sinko, PJ .
ADVANCED DRUG DELIVERY REVIEWS, 2002, 54 (03) :433-451
[13]   Changes in intragastric meal distribution are better predictors of gastric emptying rate in conscious pigs than are meal viscosity or dietary fibre concentration [J].
Guerin, S ;
Ramonet, Y ;
LeCloarec, J ;
Meunier-Salaün, MC ;
Bourguet, P ;
Malbert, CH .
BRITISH JOURNAL OF NUTRITION, 2001, 85 (03) :343-350
[14]   PHYSIOLOGICALLY-BASED PHARMACOKINETIC STUDY ON A CYCLOSPORINE DERIVATIVE, SDZ IMM-125 [J].
KAWAI, R ;
LEMAIRE, M ;
STEIMER, JL ;
BRUELISAUER, A ;
NIEDERBERGER, W ;
ROWLAND, M .
JOURNAL OF PHARMACOKINETICS AND BIOPHARMACEUTICS, 1994, 22 (05) :327-365
[15]   Assessing the dose-dependency of allometric scaling performance using physiologically based pharmacokinetic modeling [J].
Kirman, CR ;
Sweeney, LM ;
Meek, ME ;
Gargas, ML .
REGULATORY TOXICOLOGY AND PHARMACOLOGY, 2003, 38 (03) :345-367
[16]  
LUNDEEN G, 1983, ANESTH ANALG, V62, P499
[17]   METABOLISM, DISPOSITION AND EXCRETION OF [MELAMINE-C-14 IN MALE FISCHER-344 RATS [J].
MAST, RW ;
JEFFCOAT, AR ;
SADLER, BM ;
KRASKA, RC ;
FRIEDMAN, MA .
FOOD AND CHEMICAL TOXICOLOGY, 1983, 21 (06) :807-810
[18]   URINARY-BLADDER CARCINOGENESIS INDUCED BY MELAMINE IN F344 MALE-RATS - CORRELATION BETWEEN CARCINOGENICITY AND UROLITH FORMATION [J].
OGASAWARA, H ;
IMAIDA, K ;
ISHIWATA, H ;
TOYODA, K ;
KAWANISHI, T ;
UNEYAMA, C ;
HAYASHI, S ;
TAKAHASHI, M ;
HAYASHI, Y .
CARCINOGENESIS, 1995, 16 (11) :2773-2777
[19]   Assessment of melamine and cyanuric acid toxicity in cats [J].
Puschner, Birgit ;
Poppenga, Robert H. ;
Lowenstine, Linda J. ;
Filigenzi, Michael S. ;
Pesavento, Patricia A. .
JOURNAL OF VETERINARY DIAGNOSTIC INVESTIGATION, 2007, 19 (06) :616-624
[20]   INCORPORATION OF INVITRO ENZYME DATA INTO THE PHYSIOLOGICALLY-BASED PHARMACOKINETIC (PB-PK) MODEL FOR METHYLENE-CHLORIDE - IMPLICATIONS FOR RISK ASSESSMENT [J].
REITZ, RH ;
MENDRALA, AL ;
PARK, CN ;
ANDERSEN, ME ;
GUENGERICH, FP .
TOXICOLOGY LETTERS, 1988, 43 (1-3) :97-116