摘要
该试验评估了替米考星原粉和37.5%替米考星可溶性粉在肉鸡体内的药代动力学行为。将8只肉鸡随机分组,以30 mg/kg灌服替米考星原粉和37.5%替米考星可溶性粉,用UPLC-MS/MS检测血浆中替米考星的质量浓度,采用Winnonlin软件计算其药动学参数。结果表明:37.5%替米考星可溶性粉的峰浓度显著高于原粉(10.3±2.0μg/mL vs 1.4±0.4μg/mL),由此结果可推测肉鸡吸收可溶性粉的速度快于原粉。替米考星可溶性粉的AUC_(all)和AUC_(inf)均大于原粉的AUC_(all)和AUC_(inf)(31.2±9.2μg·h·mL^(-1)vs 11.7±3.2μg·h·mL^(-1);36.7±11.7μg·h·mL^(-1)vs 15.8±3.4μg·h·mL^(-1)),表明替米考星可溶性粉到达全身血液循环的量多于原粉。
The pharmacokinetic study of tilmicosin active pharmaceutical ingredients(API)and 37.5%tilmicosin soluble powder in broiler chickens were conducted.Eight healthy broiler chickens were randomly divided into two groups and they were administered at a dose of 30 mg/kg of tilmicosin API and 37.5%tilmicosin soluble powder,respectively.The plasma concentrations of tilmicosin were determined by UPLC-MS/MS and pharmacokinetic parameters were calculated by Winnonlin software.The results showed that the peak concentrations of tilmicosin soluble powder were significantly higher than that of tilmicosin API(10.3±2.0μg/mL vs 1.4±0.4μg/mL),indicating that the absorption rate of tilmicosin soluble powder was greater than that of tilmicosin API.We also found that AUC_(all) and AUCinf of the tilmicosin solublepowderwere greater than that of tilmicosin API,demonstrating that the amount of tilmicosin soluble powder reaching the whole blood circulation in broiler chickens was greater than that of the tilmicosin API.
作者
宋圣哲
王俊豪
童照寒
黄心河
杨彩梅
金庆日
SONG Shengzhe;WANG Junhao;TONG Zhaohan;HUANG Xinhe;YANG Caimei;JIN Qingri(Key Laboratory of Applied Technology of Green-Eco-Healthy Animal Husbandry of Zhejiang Province,College of Animal Science and Technology·College of Veterinary Medicine,Zhejiang A&F University,Linan Zhejiang 311300,China)
出处
《延边大学农学学报》
2022年第2期55-60,共6页
Agricultural Science Journal of Yanbian University
基金
温州宠物工程技术研究中心开放性项目资助(WP02)
浙江省基础公益研究计划(LGN20C180001)
浙江农林大学2020年校级大学生科研训练项目(2020KX0165)。