蛋白质缺乏和Tween 60对雄性Sprague-Dawley大鼠丁基羟基茴香醚及其代谢物药动学的影响。

Drug-nutrient interactions Pub Date : 1986-01-01
K Kangsadalampai, R P Sharma, M J Taylor, D K Salunkhe
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引用次数: 0

摘要

以250或2500 mg/kg体重剂量的放射性3h -丁基羟基茴香醚(BHA)口服(po)或腹腔(ip)给药,或不给药500 mg Tween 60/kg。3H-BHA在对照组和蛋白缺乏动物体内的药代动力学进行了评估。收集血液或尿液和粪便并分析3H-BHA当量。利用Autoan/Nonlin69计算机程序,BHA (250 mg/kg)的大部分药代动力学曲线符合一阶吸收的单室开放模型。唯一的例外是给药模型,其结果是一阶吸收的双室开放模型。将BHA剂量增加至2500 mg/kg,会改变BHA的药代动力学;注射后48小时未见血药浓度下降。蛋白质缺乏和Tween 60联合处理提高了BHA的吸收率。在给予2500mg /kg 3H-BHA后6.5天,3H-BHA和/或其代谢产物在尿液和粪便中完全排出。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Effect of protein deficiency and Tween 60 on the pharmacokinetics of butylated hydroxyanisole and metabolites in male Sprague-Dawley rats.

Radioactive 3H-butylated hydroxyanisole (BHA) at dosages of 250 or 2,500 mg/kg body weight was administered to rats either orally (po) or intraperitonealy (ip) with or without 500 mg Tween 60/kg. The pharmacokinetics of 3H-BHA were evaluated in both control and protein-deficient animals. Blood or urine and feces were collected and analyzed for 3H-BHA equivalents. Using the Autoan/Nonlin69 computer program, most pharmacokinetic profiles of BHA (250 mg/kg) were fit to one-compartment open models with first-order absorption. The exception was the model for ip administration, which resulted in a two-compartment open model with first-order absorption. Increasing the dose of BHA to 2,500 mg/kg altered pharmacokinetics of BHA; no decline in blood levels was observed 48 hours post-injection. Protein deficiency and Tween 60 in combination increased the rate of absorption of BHA. Excretion of 3H-BHA and/or its metabolites in urine and feces was complete 6.5 days after administration of 2,500 mg/kg 3H-BHA.

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