Raman Spectroscopy for the in Situ Identification of Cocaine and Selected Adulterants

Author:

Carter J. Chance1,Brewer William E.1,Angel S. Michael1

Affiliation:

1. Department of Chemistry and Biochemistry, University of South Carolina, Columbia, South Carolina 29208 (J.C.C., S.M.A.); and Toxicology Department, South Carolina Law Enforcement Division, 4416 Broad River Rd., Columbia, South Carolina 29210 (W.E.B.)

Abstract

We demonstrate the in situ identification of crack cocaine and cocaine·HCl by using a fiber-optic Raman probe and a portable Raman spectrograph. The Raman spectrum of freebase cocaine (crack) is obtained in just seconds without any sample preparation, and differs significantly from that of cocaine·HCl. We also show that the Raman spectra of these drugs are easily distinguishable from common cutting agents and impurities such as benzocaine and lidocaine. Another advantage of using Raman spectroscopy is that the drugs can be identified while contained in transparent containers, such as clear plastic evidence containers that are used to store drug evidence and to maintain chain of custody. We also demonstrate the in situ Raman identification of drugs separated by thin-layer chromatography. We discuss the utility of surface-enhanced Raman spectroscopy (SERS) in toxicological drug screening and present preliminary SERS data for cocaine in solution using colloidal silver. We believe this to be the first published SERS spectrum of freebase cocaine.

Publisher

SAGE Publications

Subject

Spectroscopy,Instrumentation

Reference14 articles.

1. Ellenhorn M. J. and Barceloux D. G, Medical Toxicology (Elsevier Science, New York, 1988), Chap. 28, p. 645.

2. Caplan Y. H., Cocaine, in the Abused Drugs Monograph Series, Baselt R. C. Ed. (Abbott Laboratories, Diagnostic Division, Irving, Texas, 1994), p. 3.

3. Detection of 14N and 35Cl in Cocaine Base and Hydrochloride Using NQR, NMR, and SQUID Techniques

4. Fourier transform Raman spectroscopy of illicit drugs

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