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

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

Affiliations

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

Michael L Smith et al. J Anal Toxicol. 2010 Mar.

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.

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Figures

Figure 1
Figure 1
Ecgonine (EC) can be formed by demethylation or hydrolysis of cocaine and metabolites.
Figure 2
Figure 2
Urine excretion profiles for ecgonine (EC) following four routes of cocaine administration. Cocaine doses (number of subjects) were intranasal 32 mg (n = 6); intravenous 11.2, 22.4, 25, 44.8 mg (n = 12); oral 22.4 mg (n = 6); and smoking 10, 20, 40, 42 mg (n = 12).
Figure 3
Figure 3
Concentration of cocaine, benzoylecgonine (BE), and ecgonine methyl ester (EME) after storage of aliquots of the same urine specimens at −20°C or lower for 5 years (A) and 12.7–13.2 years (B).

References

    1. Nutt D, King LA, Saulsbury W, Blakemore C. Development of a rational scale to assess the harm of drugs of potential misuse. Lancet. 2007;369:1047–1053. - PubMed
    1. Isenschmid DS. Cocaine. In: Ropero-Miller JD, Goldberger BA, editors. Handbook of Workplace Drug Testing. AACC Press; Washington, D.C.: 2009. pp. 335–354.
    1. Klette KL, Poch GK, Czarny R, Lau CO. Simultaneous GC-MS analysis of meta- and para-hydroxybenzoylecgonine and norbenzoylecgonine: a secondary method to corroborate cocaine ingestion using nonhydrolytic metabolites. J. Anal. Toxicol. 2000;24:482–488. - PubMed
    1. Cone EJ, Sampson-Cone AH, Darwin WD, Huestis MA, Oyler JM. Urine testing for cocaine abuse: metabolic and excretion patterns following different routes of administration and methods for detection of false-negative results. J. Anal. Toxicol. 2003;27:386–401. - PubMed
    1. Huestis MA, Darwin WD, Shimomura E, Lalani SA, Trinidad DV, Jenkins AJ, Cone EJ, Jacobs AJ, Smith ML, Paul BD. Cocaine and metabolites urinary excretion after controlled smoked administration. J. Anal. Toxicol. 2007;31:462–468. - PMC - PubMed

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