...
首页> 外文期刊>Journal of Analytical Toxicology >Urinary excretion of ecgonine and five other cocaine metabolites following controlled oral, intravenous, intranasal, and smoked administration of cocaine.
【24h】

Urinary excretion of ecgonine and five other cocaine metabolites following controlled oral, intravenous, intranasal, and smoked administration of cocaine.

机译:受控口服,静脉内,鼻内和抽烟可卡因后,尿中的芽子碱和其他五种可卡因代谢物排泄。

获取原文
获取原文并翻译 | 示例
   

获取外文期刊封面封底 >>

       

摘要

Urinary excretion of ecgonine (EC) was compared to that of cocaine, benzoylecgonine, ecgonine methyl ester and minor metabolites, meta-hydroxybenzoylecgonine, para-hydroxybenzoylecgonine, and norbenzoylecgonine, following controlled administration of oral, intravenous, intranasal, and smoked cocaine. Urine EC concentrations peaked later than all other analytes and had longer detection times than the other minor metabolites. With a 50 ng/mL cutoff concentration and following low doses of 10 to 45 mg cocaine by multiple routes, detection times extended up to 98 h. Maximum concentrations (Cmax) were 6-14 mole % of those for benzoylecgonine, Cmax increased with dose, time to maximum concentration (Tmax) was independent of dose, and route of administration did not have a significant impact on Cmax or Tmax for metabolites. EC is an analyte to consider for identifying cocaine use due to its stability in urine and long detection times.
机译:在控制口服,静脉内,鼻内和抽烟可卡因后,比较了可卡因,苯甲酰吗啡,艾草胺甲酯和次要代谢物,间羟基苯甲酰吗啡,对羟基苯甲酰吗啡和去甲苯甲酰吗啡的尿排泄率。尿中EC浓度的峰值晚于所有其他分析物,并且检测时间比其他次要代谢物更长。截止浓度为50 ng / mL,并通过多种途径低剂量服用10至45 mg可卡因后,检测时间延长至98 h。最大浓度(Cmax)为苯甲酰芽子碱的6-14摩尔%,Cmax随剂量增加,达到最大浓度的时间(Tmax)与剂量无关,并且给药途径对代谢物的Cmax或Tmax并无显着影响。 EC是一种可用于识别可卡因用途的分析物,因为其在尿液中的稳定性和检测时间长。

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