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1.
J Chromatogr Sci ; 54(7): 1153-8, 2016 Aug.
Artigo em Inglês | MEDLINE | ID: mdl-27406128

RESUMO

Use of unauthorized synthetic drugs is a serious, forensic, regulatory and public health issue. In this scenario, consumption of drug-impregnated blotters is very frequent. For decades, blotters have been generally impregnated with the potent hallucinogen known as lysergic acid diethylamide (LSD); however, since 2013 blotter stamps with N-2 methoxybenzyl-substituted phenylethylamine hallucinogen designated as "NBOMes" have been seized in Chile. To address this issue with readily accessible laboratory equipment, we have developed and validated a new HPTLC method for the identification and quantitation of 25-C-NBOMe in seized blotters and its confirmation by GC-MS. The proposed method was validated according to SWGTOX recommendations and is suitable for routine analysis of seized blotters containing 25-C-NBOMe. With the validated method, we analyzed 15 real samples, in all cases finding 25-C-NBOMe in a wide dosage range (701.0-1943.5 µg per blotter). In this situation, we can assume that NBOMes are replacing LSD as the main hallucinogenic drug consumed in blotters in Chile.


Assuntos
Cromatografia em Camada Fina/normas , Cromatografia Gasosa-Espectrometria de Massas/normas , Alucinógenos/isolamento & purificação , Drogas Ilícitas/isolamento & purificação , Fenetilaminas/isolamento & purificação , Administração Sublingual , Adsorção , Chile , Cromatografia em Camada Fina/métodos , Humanos , Papel , Reprodutibilidade dos Testes , Sensibilidade e Especificidade
2.
Rapid Commun Mass Spectrom ; 16(24): 2229-38, 2002.
Artigo em Inglês | MEDLINE | ID: mdl-12478565

RESUMO

A gas chromatography/mass spectrometry (GC/MS) method for the qualitative and quantitative determination of the calcium-channel antagonists C-4-substituted 1,4-dihydropyridines, and their corresponding N-ethyl derivatives, is presented. Also, the electrochemical oxidation and the reactivity of the compounds with alkyl radicals derived from 2,2'-azobis-(2-amidinopropane) were monitored by GC/MS. Mass spectral fragmentation patterns for the C-4-substituted 1,4-dihydropy-ridine parent drugs were significantly different from those of their oxidation products, generated either by electrochemical oxidation or by reaction with alkyl radicals. However, for N-ethyl-1,4-dihydropyridine compounds it was not possible to detect the final products (pyridinium salts) using these experimental conditions.


Assuntos
Bloqueadores dos Canais de Cálcio/química , Di-Hidropiridinas/química , Di-Hidropiridinas/metabolismo , Eletrólise , Cromatografia Gasosa-Espectrometria de Massas , Estrutura Molecular , Oxirredução
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