...
首页> 外文期刊>The Veterinary Journal >Pharmacokinetic and milk penetration of a difloxacin long-acting poloxamer gel formulation with carboxy-methylcellulose in lactating goats
【24h】

Pharmacokinetic and milk penetration of a difloxacin long-acting poloxamer gel formulation with carboxy-methylcellulose in lactating goats

机译:双氟沙星长效泊洛沙姆凝胶制剂与羧甲基纤维素在泌乳山羊中的药代动力学和乳汁渗透性

获取原文
获取原文并翻译 | 示例

摘要

The single-dose disposition kinetics of difloxacin were determined in clinically normal lactating goats (n = 6) after subcutaneous administration of a long-acting poloxamer 407 gel formulation with carboxy-methylcellulose (P407-CMC). Difloxacin concentrations were determined by high performance liquid chromatography with fluorescence detection. The concentration-time data were analysed by non-compartmental kinetic methods. Plasma and milk elimination half-lives after P407-CMC dosing were 35.19 h and 33.93 h, respectively. With this formulation, difloxacin achieved maximum plasma concentrations of 2.67 +/- 0.34 mg/L at 2.92 +/- 1.20 h and maximum milk concentrations of 2.31 +/- 0.35 mg/L at 4.00 +/- 0.00 h. The area under the curve (AUC) ratio AUC(milk)/AUC(plasma) was 0.89 after P407-CMC administration. It was concluded that a 15 mg/kg dose of difloxacin within P407-CMC would be effective against mastitis pathogens with a minimum inhibitory concentration (MIC) <= 0.12 mg/L
机译:在将长效泊洛沙姆407凝胶制剂与羧甲基纤维素(P407-CMC)皮下给药后,在临床上正常泌乳的山羊(n = 6)中测定了地氟沙星的单剂量处置动力学。通过高效液相色谱-荧光检测法测定地氟沙星的浓度。通过非室动力学方法分析浓度-时间数据。 P407-CMC给药后血浆和消除牛奶的半衰期分别为35.19 h和33.93 h。使用该制剂,地氟沙星在2.92 +/- 1.20 h时达到2.67 +/- 0.34 mg / L的最大血浆浓度,在4.00 +/- 0.00 h时达到2.31 +/- 0.35 mg / L的最大牛奶浓度。 P407-CMC给药后曲线下面积(AUC)比AUC(牛奶)/ AUC(血浆)为0.89。结论是,在P407-CMC中以15 mg / kg的剂量服用地氟沙星将对乳腺炎病原体有效,最小抑菌浓度(MIC)<= 0.12 mg / L

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