Carreño Gútiez Marta, Mercer Melissa A, Martínez-López Beatriz, Griffith Ronald W, Wetzlich Scott, Tell Lisa A
Department of Medicine and Epidemiology, Center for Animal Disease Modeling and Surveillance (CADMS), School of Veterinary Medicine, University of California, Davis, Davis, CA, United States.
Department of Veterinary Medicine and Epidemiology, School of Veterinary Medicine, University of California, Davis, Davis, CA, United States.
Front Vet Sci. 2024 Jul 31;11:1444009. doi: 10.3389/fvets.2024.1444009. eCollection 2024.
Prescribing fenbendazole medicated feed for pheasants in the USA is considered extra-label drug use under CPG Sec 615.115, and a safe estimated withdrawal interval (WDI) must be applied following administration to this minor food-producing species. This study sought to determine the pharmacokinetic and residue depletion profile for fenbendazole and its major metabolites to estimate a WDI for pheasants following fenbendazole administration as an oral medicated feed.
Pheasants ( = 32) were administered fenbendazole as an oral medicated feed (100 ppm) for 7 days. Fenbendazole, fenbendazole sulfoxide, and fenbendazole sulfone (FBZ-SO) in liver and muscle samples were analyzed using HPLC-UV. Tissue WDIs were estimated using FDA, European Medicines Agency (EMA), and half-life multiplication methods for US poultry tolerances, EMA maximum residue limits, and the analytical limit of detection (LOD; 0.004 ppm). Terminal tissue elimination half-lives (T) were estimated by non-compartmental analysis using a naïve pooled data approach.
The tissue T was 14.4 h for liver, 13.2 h for thigh muscle, and 14.1 h for pectoral muscle. The maximum estimated withdrawal interval was 153 h (7 days) for FBZ-SO in pectoral muscle using the FDA tolerance method (95% confidence interval for the 99 percentile of the population), and the LOD as the residue limit.
The results from this study support the use of FBZ-SO as the marker residue in the liver of pheasants and the provision of evidence based WDIs following the extra-label administration of fenbendazole medicated feed (100 ppm) for 7 days.
在美国,根据《联邦法规指南》第615.115条,给雉鸡投喂芬苯达唑药物饲料被视为超说明书用药,在给这种小型产食动物用药后,必须应用安全的估计停药期(WDI)。本研究旨在确定芬苯达唑及其主要代谢物的药代动力学和残留消除情况,以估计雉鸡经口投喂芬苯达唑药物饲料后的停药期。
32只雉鸡经口投喂含100 ppm芬苯达唑的药物饲料,持续7天。使用高效液相色谱-紫外检测法(HPLC-UV)分析肝脏和肌肉样本中的芬苯达唑、芬苯达唑亚砜和芬苯达唑砜(FBZ-SO)。采用美国食品药品监督管理局(FDA)、欧洲药品管理局(EMA)以及半衰期相乘法,分别依据美国家禽耐受量、EMA最大残留限量和分析检测限(LOD;0.004 ppm)来估计组织停药期。通过非房室分析,采用简单合并数据法估算终末组织消除半衰期(T)。
肝脏的组织半衰期为14.4小时,大腿肌肉为13.2小时,胸肌为14.1小时。使用FDA耐受量法(总体第99百分位数的95%置信区间),以LOD作为残留限量,胸肌中FBZ-SO的最大估计停药期为153小时(7天)。
本研究结果支持将FBZ-SO用作雉鸡肝脏中的标记残留,并为经口投喂7天含100 ppm芬苯达唑药物饲料后的超说明书用药提供基于证据的停药期。