» Articles » PMID: 16107742

Origin Differentiation of Heroin Sample and Its Acetylating Agent with (13)C Isotope Ratio Mass Spectrometry

Overview
Specialty Chemistry
Date 2005 Aug 19
PMID 16107742
Citations 2
Authors
Affiliations
Soon will be listed here.
Abstract

A novel method for deducing the origins of heroin and the reagent used for acetylation was established based on delta(13)C determinations of heroin and its hydrolysate, morphine, using gas chromatography (13)C isotope ratio mass spectrometry (GC-C-IRMS). The alkaline and acid hydrolysis conditions of heroin were optimized. Both yield and purity of morphine produced could meet the requirement for a GC-C-IRMS analysis. Using (2-diethylaminoethyl-2,2- diphenylvalerate) as internal standard the determinations of heroin and morphine contents were performed with a GC method in a linear range of 0.2 to 2.0 mg ml(1) that was required to gain the isotope ratio results. The hydrolysis and synthesis of heroin did not change the delta(13)C value of morphine. The precision for delta(13)C detection of both heroin and morphine was sufficient for origin differentiation of heroin samples. The information about the origins of acetylation reagents could be deduced from the difference of delta(13)C values between heroin and morphine. The results for origin differentiation of 10 heroin samples grouped into different regions and their acetylating agents were satisfactory.

Citing Articles

Forensic investigation of falsified antimalarials using isotope ratio mass spectrometry: a pilot investigation.

Newton P, Chesson L, Mayxay M, Dondorp A, Tabernero P, Howa J Sci Rep. 2024; 14(1):3995.

PMID: 38369604 PMC: 10874941. DOI: 10.1038/s41598-024-54168-9.


Stable isotope ratios and forensic analysis of microorganisms.

Kreuzer-Martin H, Jarman K Appl Environ Microbiol. 2007; 73(12):3896-908.

PMID: 17468274 PMC: 1932740. DOI: 10.1128/AEM.02906-06.