dc.contributorHelvécio Costa Menezes
dc.contributorhttp://lattes.cnpq.br/8501096347724709
dc.contributorZenilda de Lourdes Cardeal
dc.contributorBruno Gonçalves Botelho
dc.contributorWashington Xavier de Paula
dc.creatorBernardo Schmitberger Moraes
dc.date.accessioned2023-01-24T14:39:45Z
dc.date.accessioned2023-06-16T15:42:41Z
dc.date.available2023-01-24T14:39:45Z
dc.date.available2023-06-16T15:42:41Z
dc.date.created2023-01-24T14:39:45Z
dc.date.issued2022-08-17
dc.identifierhttp://hdl.handle.net/1843/49107
dc.identifier.urihttps://repositorioslatinoamericanos.uchile.cl/handle/2250/6679939
dc.description.abstractThe active ingredient of street drug ecstasy, 3,4-methylenedioxymethamphetamine (MDMA), is generally synthesized under little or no hygiene and purifications protocols, and thus a number of impurities, such as byproducts and intermediates is carried over to the final product – the tablet. To collect data on these impurities is called chemical profiling, which is a powerful tool to aid law enforcement in fighting drug trafficking. In the present work, 89 street samples, seized by Civil Police of Minas Gerais, were prepared by a harmonized method described in the literature, and analyzed by gas chromatography coupled to mass spectrometry. Out of these samples, 38 were prepared by direct immersion solid-phase microextraction (DI-SPME), with a divinylbenzene-polydimethylsiloxane-coated fiber, to evaluate this technique’s feasibility, whose parameters were optimized by a multivariate design. In total, 72 different chemical species were detected in the 89 samples; principal component analyses, hierarchical cluster analyses and correlation metrics were performed. Profiling by the harmonized method revealed similarities among samples whose tablets were physically different, which would go unnoticed in routine analyses. It also showed that samples with nearly identical tablets can have different origins. Besides that, it was noticed a unusually high content of 3,4-methylenedioxyphenylpropan-2-ol, a MDMA synthesis byproduct, in some samples. Some synthesis route-specific compounds were also detected in certain samples. Regardind the DI-SPME optimization, four factors were relevant: pH, desorption time, sample mass and extraction time. DI-SPME proved itself promising in the context of profiling by providing results comparable to those of the harmonized method. In all cases, relative standard deviation and retention time shift were acceptable. It was concluded that profiling is a promising tool in fighting drug trafficking in Brazil.
dc.publisherUniversidade Federal de Minas Gerais
dc.publisherBrasil
dc.publisherICX - DEPARTAMENTO DE QUÍMICA
dc.publisherPrograma de Pós-Graduação em Química
dc.publisherUFMG
dc.rightsAcesso Aberto
dc.subjectPerfilamento
dc.subjectEcstasy
dc.subject3,4-metilenodioximetanfetamina MDMA
dc.subjectGC/MS
dc.subjectMicroextração em fase sólida por imersão direta
dc.subjectProfiling
dc.subjectDirect immersion solid-phase microextraction (DI-SPME)
dc.subjectCromatografia gasosa acoplada à espectrometria de massas
dc.subjectCromatografia gasosa
dc.subjectEspectrometria de massa
dc.titlePerfilamento de impurezas em amostras de ecstasy apreendidas em Minas Gerais utilizando microextração em fase sólida e análise por cromatografia gasosa acoplada à espectrometria de massas
dc.typeDissertação


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