...
首页> 外文期刊>Journal of animal and veterinary advances >The Usefulness of Saliva as a Biological Material for the Determination of Pharmacokinetics of Model Drugs (Antipyrine, Caffeine, Paracetamol) in Calves: Comparative Study
【24h】

The Usefulness of Saliva as a Biological Material for the Determination of Pharmacokinetics of Model Drugs (Antipyrine, Caffeine, Paracetamol) in Calves: Comparative Study

机译:唾液作为生物材料测定犊牛模型药物(安替比林,咖啡因,扑热息痛)药代动力学的有用性:比较研究

获取原文
           

摘要

The aim of this study was to evaluate usefulness of saliva as a biological material for determination of pharmacokinetics of model drugs (antipyrine, caffeine and paracetamol) in calves at different age. For the experiment, 30 Black and White calves (BW) at the age of 10 and 40 days were divided into three groups. The calves of group I received antipyrine (10 mg kg-1 bw.), group II caffeine (5 mg kg-1 bw.) and group III paracetamol (10 mg kg-1 bw.). Samples of blood and saliva were collected from all examined animals. The concentration of antipyrine and paracetamol was measured spectrophotometrically. The concentration of caffeine was evaluated by EMIT method. The pharmacokinetics of antipyrine were estimated using one-compartment model whereas the pharmacokinetics of caffeine and paracetamol using non-compartment model. The following pharmacokinetic parameters were evaluated: volume of distribution, relative volume of distribution, mean residence time; biological half-life, metabolic clearance, relative metabolic clearance and level of model drugs-plasma proteins fractions. Results obtained in the experiment (not statistically significant differences in pharmacokinetic parameter values of antipyrine and caffeine and statistically significant according to paracetamol) determined on the basis of model drugs concentration in blood and saliva showed that saliva has potential to be used as a biological material from calves but only for evaluation of pharmacokinetics of antipyrine and caffeine. However, it cannot be used for assessment of pharmacokinetics of paracetamol.
机译:这项研究的目的是评估唾液作为确定不同年龄犊牛模型药物(安替比林,咖啡因和扑热息痛)的药代动力学的生物材料的有用性。对于该实验,将30只10和40天龄的黑白犊牛(BW)分为三组。第一组的犊牛接受安替比林(10 mg kg-1 bw。),第二组咖啡因(5 mg kg-1 bw。)和第三组扑热息痛(10 mg kg-1 bw。)。从所有检查的动物中采集血液和唾液样品。分光光度法测定安替比林和扑热息痛的浓度。通过EMIT方法评估咖啡因的浓度。使用一室模型评估安替比林的药代动力学,而使用非室模型评估咖啡因和扑热息痛的药代动力学。评价以下药代动力学参数:分布体积,相对分布体积,平均停留时间;生物半衰期,代谢清除率,相对代谢清除率和模型药物-血浆蛋白组分的水平。根据模型药物在血液和唾液中的浓度确定的实验结果(安替比林和咖啡因的药代动力学参数值在统计学上无显着差异,而对乙酰氨基酚的统计学意义上无统计学意义)表明,唾液具有作为生物材料的潜力小牛,但仅用于评估安替比林和咖啡因的药代动力学。但是,它不能用于评估扑热息痛的药代动力学。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号