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1.
Drug Test Anal ; 10(11-12): 1657-1669, 2018 Nov.
Artículo en Inglés | MEDLINE | ID: mdl-30341930

RESUMEN

Zebrafish (Danio rerio) water tank (ZWT) approach was investigated as an alternative model for metabolism studies based on six different experiments with four model compounds. Sibutramine was applied for the multivariate optimization of ZWT conditions, also for the comparison of the metabolism among ZWT, humans and mice, beyond for the role of CYP2B6 in ZWT. After the optimization, 18 fish and 168 hours of experiments is the minimum requirement for a relevant panel of biotransformation products. A comparison among the species resulted in the observation of the same hydroxylated metabolites, with differences in metabolites concentration ratio. However, the ZWT allowed tuning of the conditions to obtain a specific metabolic profile, depending on the need. In addition, by utilizing CYP2B6 inhibition, a relevant ZWT pathway for the demethylation of drugs was determined. The stereospecificity of the ZWT metabolism was investigated using selegiline and no racemization or inversion transformations were observed. Moreover, the investigation of metabolism of cannabimimetics was performed using JWH-073 and the metabolites observed are the same described for humans, except for the hydroxylation at the indol group, which was explained by the absence of CYP2C9 orthologs in zebrafish. Finally, hexarelin was used as a model to evaluate studies by ZWT for drugs with low stability. As a result, hexarelin displays a very fast metabolization in ZWT conditions and all the metabolites described for human were observed in ZWT. Therefore, the appropriate conditions, merits, and relevant limitations to conduct ZWT experiments for the investigation of drug metabolism are described.


Asunto(s)
Preparaciones Farmacéuticas/metabolismo , Pez Cebra/metabolismo , Adulto , Animales , Antidepresivos/metabolismo , Antidepresivos/orina , Biotransformación , Ciclobutanos/metabolismo , Ciclobutanos/orina , Citocromo P-450 CYP2B6/metabolismo , Inhibidores del Citocromo P-450 CYP2B6/farmacología , Femenino , Humanos , Hidroxilación , Indoles/metabolismo , Indoles/orina , Masculino , Ratones , Modelos Animales , Naftalenos/metabolismo , Naftalenos/orina , Oligopéptidos/metabolismo , Oligopéptidos/orina , Preparaciones Farmacéuticas/orina , Selegilina/metabolismo , Selegilina/orina , Pez Cebra/orina , Proteínas de Pez Cebra/metabolismo
2.
Drug Test Anal ; 9(11-12): 1658-1672, 2017 Nov.
Artículo en Inglés | MEDLINE | ID: mdl-29078043

RESUMEN

This paper summarises the results obtained from the doping control analyses performed during the Summer XXXI Olympic Games (August 3-21, 2016) and the XV Paralympic Games (September 7-18, 2016). The analyses of all doping control samples were performed at the Brazilian Doping Control Laboratory (LBCD), a World Anti-Doping Agency (WADA)-accredited laboratory located in Rio de Janeiro, Brazil. A new facility at Rio de Janeiro Federal University (UFRJ) was built and fully operated by over 700 professionals, including Brazilian and international scientists, administrative staff, and volunteers. For the Olympic Games, 4913 samples were analysed. In 29 specimens, the presence of a prohibited substance was confirmed, resulting in adverse analytical findings (AAFs). For the Paralympic Games, 1687 samples were analysed, 12 of which were reported as AAFs. For both events, 82.8% of the samples were urine, and 17.2% were blood samples. In total, more than 31 000 analytical procedures were conducted. New WADA technical documents were fully implemented; consequently, state-of-the-art analytical toxicology instrumentation and strategies were applied during the Games, including different types of mass spectrometry (MS) analysers, peptide, and protein detection strategies, endogenous steroid profile measurements, and blood analysis. This enormous investment yielded one of the largest Olympic legacies in Brazil and South America. Copyright © 2017 John Wiley & Sons, Ltd.


Asunto(s)
Doping en los Deportes , Detección de Abuso de Sustancias/métodos , Brasil , Humanos , Espectrometría de Masas , América del Sur
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