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可卡因经口服、静脉注射、鼻吸和吸烟给药后,尿液中 ecgonine 及其他五种可卡因代谢物的排泄。

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

机构信息

Division of Forensic Toxicology, Armed Forces Medical Examiner System, Armed Forces Institute of Pathology, Rockville, Maryland, USA.

出版信息

J Anal Toxicol. 2010 Mar;34(2):57-63. doi: 10.1093/jat/34.2.57.

Abstract

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.

摘要

尿中 ecgonine(EC)的排泄与可卡因、苯甲酰 ecgonine、ecgonine 甲酯和其他次要代谢物(meta-hydroxybenzoylecgonine、para-hydroxybenzoylecgonine 和 norbenzoylecgonine)进行比较,这些代谢物是在口服、静脉内、鼻内和吸烟可卡因给药后产生的。尿液 EC 浓度峰值晚于所有其他分析物,且检测时间长于其他次要代谢物。当以 50ng/mL 的截止浓度和 10 至 45mg 可卡因的低剂量通过多种途径给药时,检测时间可延长至 98 小时。最大浓度(Cmax)为苯甲酰 ecgonine 的 6-14 摩尔%,Cmax 随剂量增加而增加,达峰时间(Tmax)与剂量无关,且给药途径对代谢物的 Cmax 或 Tmax 没有显著影响。EC 是一种用于识别可卡因使用的分析物,因为它在尿液中的稳定性和较长的检测时间。

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