Electroanalytical profiling of cocaine samples by means of an electropolymerized molecularly imprinted polymer using benzocaine as the template molecule

Author(s)

Grothe, Renata A. ^[1] ; Lobato, Alnilan ^[1] ; Mounssef, Bassim ^[1] ; Tasi, Nikola ^[1] ; Braga, Ataualpa A. C. ^[1] ; Maldaner, Adriano O. ^[2] ; Aldous, Leigh ^[3] ; Paixao, Thiago R. L. C. ^[1] ; Goncalves, Luis Moreira ^[1]

Affiliation

^[1] Univ Sao Paulo, Inst Quim, Dept Quim Fundamental, Ave Prof Lineu Prestes 748, Cidade Univ, BR-05508000 Sao Paulo, SP - Brazil

^[2] Policia Fed Brasileira PFB, Inst Nacl Criminalist, Q7, L23, BR-70610200 Brasilia, DF - Brazil

^[3] Kings Coll London, Dept Chem, Britannia House, 7 Trinity St, London SE1 1DB - England

• Document type: Journal article
• Source: ANALYST; v. 146, n. 5, p. 1747-1759, MAR 7 2021.
• Web of Science Citations: 1

Abstract

The analysis of `cutting' or additive agents in cocaine, like benzocaine (BZC), allows police analysts to identify each component of the sample, thus obtaining information like the drugs' provenience. This kind of drug profiling is of great value in tackling drug trafficking. Electropolymerized molecularly imprinted polymers (e-MIPs) on portable screen-printed carbon electrodes (SPCEs) were developed in this study for BZC determination. The MIPs' electropolymerization was performed on a carbon surface using the anaesthetic BZC as the template molecule and 3-amino-4-hydroxybenzoic acid (3,4-AHBA) as the functional monomer. The build-up of this biomimetic sensor was carefully characterized by cyclic voltammetry (CV) and optimized. Cyclic voltammetric investigation demonstrated that BZC oxidation had a complex and pH-dependent mechanism, but at pH 7.4 a single, well-defined oxidation feature was observed. The BZC-MIP interactions were studied by computer-aided theoretical modeling by means of density functional theory (DFT) calculations. The electroanalytical methodology was effectively applied to artificial urine samples; BZC molecular recognition was achieved with a low limit of detection (LOD) of 2.9 nmol L-1 employing square-wave voltammetry (SWV). The e-MIPs were then used to `fingerprint' genuine cocaine samples, assisted by principal component analysis (PCA), at the central forensic laboratory of the Brazilian Federal Police (BFP) with a portable potentiostat. This electroanalysis provided proof-of-concept that the drugs could be voltammetrically `fingerprinted' using e-MIPs supported by chemometric analysis. (AU)

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• Support Opportunities: Scholarships in Brazil - Post-Doctoral
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• Support Opportunities: Research Grants - Young Investigators Grants
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