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1.
Forensic Sci Int ; 304: 109969, 2019 Nov.
Artículo en Inglés | MEDLINE | ID: mdl-31593907

RESUMEN

The new psychoactive substances (NPS) in Colombia are detected by national authorities, in blotters strip, in different circumstances and places: airports, music concerts, discos and parks. Blotters are marketed as LSD and cause several cases of intoxication and death in some consumers: due to acute intoxication or when mixed with other drugs and may have different effects on the central nervous system (CNS). This study was conducted to research into and identify the chemical composition of the drugs impregnated in the blotters sold in two Colombian cities. This research provides the analysis of 70 doses coming from forensic cases of the Colombian Attorney General's Office in Bogota and from the Laboratory of Narcotics of the Colombian National Institute of Legal Medicine and Forensic Sciences (North Headquarter) in Barranquilla. Mixtures of drugs, such as DOB, 25I-NBOMe, MDMA and 25I-NBOMe imine were found within the blotters through gas chromatography coupled to mass spectrometry (CGMS); these drugs are classified by international authorities as NPS belonging to the phenylethylamines group. The results clearly warn about a growing public health problem in the country.


Asunto(s)
2,5-Dimetoxi-4-Metilanfetamina/análogos & derivados , Dimetoxifeniletilamina/análogos & derivados , Tráfico de Drogas , Drogas Ilícitas/aislamiento & purificación , N-Metil-3,4-metilenodioxianfetamina/aislamiento & purificación , 2,5-Dimetoxi-4-Metilanfetamina/aislamiento & purificación , Administración Sublingual , Colombia , Drogas de Diseño/aislamiento & purificación , Dimetoxifeniletilamina/aislamiento & purificación , Contaminación de Medicamentos , Humanos , Papel , Trastornos Relacionados con Sustancias
2.
Anal Chem ; 89(3): 1445-1452, 2017 02 07.
Artículo en Inglés | MEDLINE | ID: mdl-28059498

RESUMEN

The NBOMe derivatives are phenethylamines derived from the 2C class of hallucinogens. Only a few human pharmacologic studies have been conducted on these drugs, and several cases of intoxication and deaths have been reported. Presently, NBOMe are not a part of the routine drugs-of-abuse screening procedure for many police forces, and there are no rapid immunoassay screening tests that can detect the presence of those compounds. In this Article, the voltammetric behavior of 25B NBOMe and 25I NBOMe were investigated and their electroanalytical characteristics determined for the first time. A novel, fast, and sensitive screening method for the identification of the two most common NBOMes (25B-NBOMe and 25I-NBOMe) in real samples is reported. The method uses the electrochemical oxidation of these molecules to produce an analytical signal that can be related to the NBOMe concentration with an average lower limit of quantitation of 0.01 mg/mL for both of them. The method is selective enough to identify the two compounds individually, even given the great similarity in their structure.


Asunto(s)
Técnicas Electroquímicas/métodos , Fenetilaminas/análisis , Psicotrópicos/análisis , Anisoles/análisis , Dimetoxifeniletilamina/análogos & derivados , Dimetoxifeniletilamina/análisis , Medicina Legal , Concentración de Iones de Hidrógeno , Límite de Detección , Fenetilaminas/química , Psicotrópicos/química
5.
Br J Pharmacol ; 141(7): 1167-74, 2004 Apr.
Artículo en Inglés | MEDLINE | ID: mdl-15006903

RESUMEN

1. We recently described that several 2-(2,5-dimethoxy-4-substituted phenyl)ethylamines (PEAs), including 4-I=2C-I, 4-Br=2C-B, and 4-CH(3)=2C-D analogs, are partial agonists at 5-HT(2C) receptors, and show low or even negligible intrinsic efficacy at 5-HT(2A) receptors. These results raised the proposal that these drugs may act as 5-HT(2) antagonists. 2. To test this hypothesis, Xenopus laevis oocytes were microinjected with the rat clones for 5-HT(2A) or 5-HT(2C) receptors. The above-mentioned PEAs and its 4-H analog (2C-H) blocked the 5-HT-induced currents at 5-HT(2A), but not at the 5-HT(2C) receptor, revealing 5-HT(2) receptor subtype selectivity. The 5-HT(2A) receptor antagonism required a 2-min preincubation to attain maximum inhibition. 3. All PEAs tested shifted the 5-HT concentration-response curves to the right and downward. Their potencies varied with the nature of the C(4) substituent; the relative rank order of their 5-HT(2A) receptor antagonist potency was 2C-I>2C-B>2C-D>2C-H. 4. The present results demonstrate that in X. laevis oocytes, a series of 2,5-dimethoxy-4-substituted PEAs blocked the 5-HT(2A) but not the 5-HT(2C) receptor-mediated responses. As an alternative hypothesis, we suggest that the psychostimulant activity of the PEAs may not be exclusively associated with partial or full 5-HT(2A) receptor agonism.


Asunto(s)
Dimetoxifeniletilamina/análogos & derivados , Dimetoxifeniletilamina/farmacología , Oocitos/efectos de los fármacos , Fenetilaminas/farmacología , Antagonistas del Receptor de Serotonina 5-HT2 , Relación Estructura-Actividad , Xenopus laevis/metabolismo , Animales , Clonación Molecular , Antagonismo de Drogas , Microinyecciones , Oocitos/metabolismo , Fenetilaminas/química , Fenetilaminas/clasificación , Ratas , Receptor de Serotonina 5-HT2A/administración & dosificación , Receptor de Serotonina 5-HT2A/genética , Receptor de Serotonina 5-HT2C/administración & dosificación , Receptor de Serotonina 5-HT2C/genética , Receptor de Serotonina 5-HT2C/aislamiento & purificación
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