Institute of Computational Comparative Medicine (ICCM), Department of Anatomy and Physiology, College of Veterinary Medicine, Kansas State University, Manhattan, KS 66506, USA.
Department of Statistics, College of Arts and Sciences, Kansas State University, Manhattan, KS 66506, USA.
Sci Rep. 2016 Jun 15;6:27907. doi: 10.1038/srep27907.
Violative drug residues in animal-derived foods are a global food safety concern. The use of a fixed main metabolite to parent drug (M/D) ratio determined in healthy animals to establish drug tolerances and withdrawal times in diseased animals results in frequent residue violations in food-producing animals. We created a general physiologically based pharmacokinetic model for representative drugs (ceftiofur, enrofloxacin, flunixin, and sulfamethazine) in cattle and swine based on extensive published literature. Simulation results showed that the M/D ratio was not a fixed value, but a time-dependent range. Disease changed M/D ratios substantially and extended withdrawal times; these effects exhibited drug- and species-specificity. These results challenge the interpretation of violative residues based on the use of the M/D ratio to establish tolerances for metabolized drugs.
动物源性食品中的违规药物残留是一个全球性的食品安全问题。使用在健康动物中确定的固定母体药物(M)与主要代谢物(D)比值来制定患病动物的药物耐受和停药时间,这导致了在生产食品的动物中经常出现残留违规问题。我们根据广泛发表的文献,为牛和猪中的代表性药物(头孢噻呋、恩诺沙星、氟尼辛和磺胺二甲嘧啶)创建了一个通用的基于生理学的药代动力学模型。模拟结果表明,M/D 比值不是一个固定值,而是一个随时间变化的范围。疾病大大改变了 M/D 比值并延长了停药时间;这些影响表现出药物和物种特异性。这些结果挑战了基于使用 M/D 比值来为代谢药物制定耐受标准的残留违规解释。