» Articles » PMID: 7815031

Detection of Cocaine, Norcocaine, and Cocaethylene in the Meconium of Premature Neonates

Overview
Journal J Forensic Sci
Specialty Forensic Sciences
Date 1994 Nov 1
PMID 7815031
Citations 5
Authors
Affiliations
Soon will be listed here.
Abstract

Our objective was to investigate the methodologic detection of cocaine abuse during pregnancy by determining the viability of meconium analysis for cocaine and its metabolites using chromatographic procedures as an alternative to urine testing using enzyme multiplied immunoassay technique. Our design was as follows: meconium and urine were taken from 106 very low birthweight premature babies. Meconium analysis for cocaine and its metabolites using extraction and chromatographic analysis was compared with the criterion standard immunoassay testing for urine. The work was carried out at The University of Chicago Hospital, Department of Pediatrics and the University of Illinois at Chicago, Department of Pharmacodynamics. Our patients were very low birthweight, premature babies (mean birthweight 1109 g; mean gestational age 29.1 weeks). Gender was evenly divided between male and female. The outcome measures were as follows: two active metabolites, norcocaine and cocaethylene, were detected in the meconium, but not in the urine, of some of the neonates. Determination of cocaine exposure in the newborn influenced assignment of babies in research studies as well as psychosocial evaluation and subsequent treatment of the neonate. Our results were: of the 106 meconium samples analyzed, 21 (19.8%) were positive for cocaine (n = 19, 0.24-0.78 mg/kg), norcocaine (n = 7, 0.10-0.56 mg/kg), cocaethylene (n = 1, 0.12 mg/kg) or combinations thereof. Benzoylecgonine was not detected in any of the samples. Of the urine samples analyzed by immunoassay, only 8 (7.5%) were positive for cocaine metabolites. We conclude that meconium is a better sample than urine for determining cocaine exposure in utero.(ABSTRACT TRUNCATED AT 250 WORDS)

Citing Articles

A biomarker validation study of prenatal chlorpyrifos exposure within an inner-city cohort during pregnancy.

Whyatt R, Garfinkel R, Hoepner L, Andrews H, Holmes D, Williams M Environ Health Perspect. 2009; 117(4):559-67.

PMID: 19440494 PMC: 2679599. DOI: 10.1289/ehp.0800041.


Development and validation of a liquid chromatography-atmospheric pressure chemical ionization-tandem mass spectrometry method for simultaneous analysis of 10 amphetamine-, methamphetamine- and 3,4-methylenedioxymethamphetamine-related (MDMA)....

Kelly T, Gray T, Huestis M J Chromatogr B Analyt Technol Biomed Life Sci. 2008; 867(2):194-204.

PMID: 18424195 PMC: 2587330. DOI: 10.1016/j.jchromb.2008.03.029.


Substance use during pregnancy: time for policy to catch up with research.

Lester B, Andreozzi L, Appiah L Harm Reduct J. 2004; 1(1):5.

PMID: 15169566 PMC: 419718. DOI: 10.1186/1477-7517-1-5.


Use of biomarkers to indicate exposure of children to organophosphate pesticides: implications for a longitudinal study of children's environmental health.

Wessels D, Barr D, Mendola P Environ Health Perspect. 2003; 111(16):1939-46.

PMID: 14644670 PMC: 1241770. DOI: 10.1289/ehp.6179.


Measurement of organophosphate metabolites in postpartum meconium as a potential biomarker of prenatal exposure: a validation study.

Whyatt R, Barr D Environ Health Perspect. 2001; 109(4):417-20.

PMID: 11335191 PMC: 1240283. DOI: 10.1289/ehp.01109417.