Análise da distribuição espacial de designer drugs em selos por MALDI FT-ICR Imaging MS

Detalhes bibliográficos
Ano de defesa: 2020
Autor(a) principal: Almeida, Camila Medeiros de
Orientador(a): Romão, Wanderson lattes
Banca de defesa: Lopes, Norberto Peporine lattes, Borges, Warley de Souza lattes
Tipo de documento: Dissertação
Tipo de acesso: Acesso aberto
Idioma: por
Instituição de defesa: Universidade Federal do Espírito Santo
Mestrado em Química
Programa de Pós-Graduação: Programa de Pós-Graduação em Química
Departamento: Centro de Ciências Exatas
País: BR
Palavras-chave em Português:
Área do conhecimento CNPq:
Link de acesso: http://repositorio.ufes.br/handle/10/15001
Resumo: The phenethylamines derivatives, the NBOMes, N-bomb or Smiles, are potent hallucinogens, which are often sold as blotter paper. Changes in their molecular structures are constantly carried out, such as the exchange of halogen in the carbon 4 (C4) or the substitution of the methyl to a hydroxyl, observed in the modification of NBOMe to NBOH. This happens so that the new substances are not classified as illicit and preserved the psychoactive effects of molecules. In order to follow the dynamics of designer drugs market, the use of different analytical methods for the identification of these substances has been a solution. In this study, the matrix assisted laser desorption/ionization mass spectrometry (MALDI MS) and MALDI mass spectrometry imaging (MALDI MSI) were coupled to a Fourier transform ion cyclotron resonance mass spectrometer (FT-ICR MS) and used to analyze seven blotter papers of NBOMes containing 25I-NBOH (2-({[2-(4-iodo-2,5- dimethoxyphenyl) ethyl]amino}methyl) phenol, m/z 414,05) and 25I-NBOMe ((2-(4-iodo-2,5-dimethoxyphenyl)-N-[(2 methoxyphenyl) methyl]ethanamine), m/z 428,07). An optimization study was performed to evaluate the matrix application (pipette versus sprayer assisted by an ESI probe); the matrices (α-cyano-4-hydroxycinnamic acid (CHCA), 2,5 dihydroxybenzoic acid (DHB), 7,7,8,8-tetracyanoquinodimethane (TCNQ) and sinapinic acid (SA)) effect in the process of desorption and ionization and their concentration (from 5 to 25 mg.mL−1). After, a study of the spatial distribution of the NBOMes derivatives detected in the front and back of the blotter paper surface was performed. MALDI MS and MALDI MSI results showed that the matrix sprayer was the best method for matrix application, which allowed a homegeneous detection of the compound when compared to the pipette application. The CHCA matrix, in a concentration ≥ 15 mg.mL−1, displayed a higher ionization efficiency of the 25I-NBOMe compound, commonly detected in blotter paper, where an intense distribution was observed in relation to others matrices. The distribution of the active ingredient studied in the front and back between the six blotter papers analyzed showed that the three of them had a higher concentration of the active ingredient in only one of the sides (two in the back and one in the front), while the others presented a similar distribution in both sides.
id UFES_bc3dce136222dcf0a5ed5b41e27c7d2f
oai_identifier_str oai:repositorio.ufes.br:10/15001
network_acronym_str UFES
network_name_str Repositório Institucional da Universidade Federal do Espírito Santo (riUfes)
repository_id_str
spelling Romão, Wandersonhttps://orcid.org/0000000222546683http://lattes.cnpq.br/9121022613112821Almeida, Camila Medeiros dehttps://orcid.org/0000-0003-3318-8583http://lattes.cnpq.br/4627760102080131Lopes, Norberto Peporinehttps://orcid.org/0000-0002-8159-3658http://lattes.cnpq.br/1357061371579771Borges, Warley de Souzahttps://orcid.org/0000000344751028http://lattes.cnpq.br/97424022859704292024-05-30T00:49:48Z2024-05-30T00:49:48Z2020-02-18The phenethylamines derivatives, the NBOMes, N-bomb or Smiles, are potent hallucinogens, which are often sold as blotter paper. Changes in their molecular structures are constantly carried out, such as the exchange of halogen in the carbon 4 (C4) or the substitution of the methyl to a hydroxyl, observed in the modification of NBOMe to NBOH. This happens so that the new substances are not classified as illicit and preserved the psychoactive effects of molecules. In order to follow the dynamics of designer drugs market, the use of different analytical methods for the identification of these substances has been a solution. In this study, the matrix assisted laser desorption/ionization mass spectrometry (MALDI MS) and MALDI mass spectrometry imaging (MALDI MSI) were coupled to a Fourier transform ion cyclotron resonance mass spectrometer (FT-ICR MS) and used to analyze seven blotter papers of NBOMes containing 25I-NBOH (2-({[2-(4-iodo-2,5- dimethoxyphenyl) ethyl]amino}methyl) phenol, m/z 414,05) and 25I-NBOMe ((2-(4-iodo-2,5-dimethoxyphenyl)-N-[(2 methoxyphenyl) methyl]ethanamine), m/z 428,07). An optimization study was performed to evaluate the matrix application (pipette versus sprayer assisted by an ESI probe); the matrices (α-cyano-4-hydroxycinnamic acid (CHCA), 2,5 dihydroxybenzoic acid (DHB), 7,7,8,8-tetracyanoquinodimethane (TCNQ) and sinapinic acid (SA)) effect in the process of desorption and ionization and their concentration (from 5 to 25 mg.mL−1). After, a study of the spatial distribution of the NBOMes derivatives detected in the front and back of the blotter paper surface was performed. MALDI MS and MALDI MSI results showed that the matrix sprayer was the best method for matrix application, which allowed a homegeneous detection of the compound when compared to the pipette application. The CHCA matrix, in a concentration ≥ 15 mg.mL−1, displayed a higher ionization efficiency of the 25I-NBOMe compound, commonly detected in blotter paper, where an intense distribution was observed in relation to others matrices. The distribution of the active ingredient studied in the front and back between the six blotter papers analyzed showed that the three of them had a higher concentration of the active ingredient in only one of the sides (two in the back and one in the front), while the others presented a similar distribution in both sides.Os derivados feniletilamínicos, conhecidos como NBOMes, são potentes alucinógenos, frequentemente comercializados como selos. Mudanças em suas estruturas moleculares são constantemente realizadas, como a troca do halogênio ligado ao carbono 4 (C4) ou a substituição do grupo metil por uma hidroxila, observado na modificação do NBOMe e formação do NBOH, sempre conservando os efeitos psicoativos das moléculas. Neste estudo, a técnica de espectrometria de massa (mass spectrometry – MS) por ionização/dessorção a laser assistida por matriz, (matrix assisted laser desorption/ionization - MALDI), e espectrometria de massa de imagem (mass spectrometry imaging - MSI), acoplado ao espectrômetro de massa de ressonância de íon ciclotrônica com transformada de fourier, foi utilizada para analisar selos contendo 25I- NBOH (2 - ({[2- (4-iodo-2,5-dimetoxifenil) etil] amino} metil) fenol, m/z 414,05) e 25I- NBOMe ((2- (4-iodo-2,5-dimetoxifenil) -N - [(2- metoxifenil) metil] etanamina), m/z 428,07). Um estudo de otimização foi realizado para avaliar a aplicação da matriz (pipeta automática versus pulverizador assistido por um probe da fonte ESI); o efeito das matrizes (ácido α-ciano-4-hidroxicinâmico (CHCA), ácido 2,5 di-hidroxibenzóico (DHB), 7,7,8,8-tetracianoquinodimetano (TCNQ) e ácido sinápico(SA)) no processo de ionização e dessorção; e sua concentração (de 5 a 25 mg.mL−1). Posteriormente, foi realizado um estudo da distribuição espacial dos derivados NBOMes detectados sobre a superfície da frente e do verso do selo. Os resultados de MALDI MS e MALDI MSI mostraram que o melhor método de aplicação da matriz foi utilizando o pulverizador, no qual permitiu uma detecção homogênea do composto quando comparado a aplicação com a pipeta automática. A matriz CHCA, com concentração ≥ 15 mg.mL−1, apresentou maior eficiência de ionização do composto 25I-NBOMe, comumente detectado em selos, onde uma distribuição homogênea e intensa foi observada em relação a outras matrizes. A distribuição do composto psicoativo estudado na frente e no verso dos selos analisados mostraram que três apresentavam maior concentração do composto em um dos lados (dois no verso e um na frente), enquanto os demais apresentavam distribuição em ambos os lados.Fundação Coordenação de Aperfeiçoamento de Pessoal de Nível Superior (CAPES)Texthttp://repositorio.ufes.br/handle/10/15001porUniversidade Federal do Espírito SantoMestrado em QuímicaPrograma de Pós-Graduação em QuímicaUFESBRCentro de Ciências Exatassubject.br-rjbnQuímicaDesigner drugs25I-NBOMe25I-NBOHMALDI MSIAnálise da distribuição espacial de designer drugs em selos por MALDI FT-ICR Imaging MSMALDI FT-ICR imaging MS analysis of designer drugs distribution in blotter papersinfo:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/masterThesisinfo:eu-repo/semantics/openAccessreponame:Repositório Institucional da Universidade Federal do Espírito Santo (riUfes)instname:Universidade Federal do Espírito Santo (UFES)instacron:UFESORIGINALCamilaMedeirosdeAlmeida-2020-dissertacao-livre.pdfapplication/pdf4192323http://repositorio.ufes.br/bitstreams/4602791f-7cb3-4007-a9e6-caef52a792b1/download7a9840acd8e997d25b5904613724feefMD5110/150012025-07-11 13:50:46.608oai:repositorio.ufes.br:10/15001http://repositorio.ufes.brRepositório InstitucionalPUBhttp://repositorio.ufes.br/oai/requestriufes@ufes.bropendoar:21082025-07-11T13:50:46Repositório Institucional da Universidade Federal do Espírito Santo (riUfes) - Universidade Federal do Espírito Santo (UFES)false
dc.title.none.fl_str_mv Análise da distribuição espacial de designer drugs em selos por MALDI FT-ICR Imaging MS
dc.title.alternative.none.fl_str_mv MALDI FT-ICR imaging MS analysis of designer drugs distribution in blotter papers
title Análise da distribuição espacial de designer drugs em selos por MALDI FT-ICR Imaging MS
spellingShingle Análise da distribuição espacial de designer drugs em selos por MALDI FT-ICR Imaging MS
Almeida, Camila Medeiros de
Química
Designer drugs
25I-NBOMe
25I-NBOH
MALDI MSI
subject.br-rjbn
title_short Análise da distribuição espacial de designer drugs em selos por MALDI FT-ICR Imaging MS
title_full Análise da distribuição espacial de designer drugs em selos por MALDI FT-ICR Imaging MS
title_fullStr Análise da distribuição espacial de designer drugs em selos por MALDI FT-ICR Imaging MS
title_full_unstemmed Análise da distribuição espacial de designer drugs em selos por MALDI FT-ICR Imaging MS
title_sort Análise da distribuição espacial de designer drugs em selos por MALDI FT-ICR Imaging MS
author Almeida, Camila Medeiros de
author_facet Almeida, Camila Medeiros de
author_role author
dc.contributor.authorID.none.fl_str_mv https://orcid.org/0000-0003-3318-8583
dc.contributor.authorLattes.none.fl_str_mv http://lattes.cnpq.br/4627760102080131
dc.contributor.advisor1.fl_str_mv Romão, Wanderson
dc.contributor.advisor1ID.fl_str_mv https://orcid.org/0000000222546683
dc.contributor.advisor1Lattes.fl_str_mv http://lattes.cnpq.br/9121022613112821
dc.contributor.author.fl_str_mv Almeida, Camila Medeiros de
dc.contributor.referee1.fl_str_mv Lopes, Norberto Peporine
dc.contributor.referee1ID.fl_str_mv https://orcid.org/0000-0002-8159-3658
dc.contributor.referee1Lattes.fl_str_mv http://lattes.cnpq.br/1357061371579771
dc.contributor.referee2.fl_str_mv Borges, Warley de Souza
dc.contributor.referee2ID.fl_str_mv https://orcid.org/0000000344751028
dc.contributor.referee2Lattes.fl_str_mv http://lattes.cnpq.br/9742402285970429
contributor_str_mv Romão, Wanderson
Lopes, Norberto Peporine
Borges, Warley de Souza
dc.subject.cnpq.fl_str_mv Química
topic Química
Designer drugs
25I-NBOMe
25I-NBOH
MALDI MSI
subject.br-rjbn
dc.subject.por.fl_str_mv Designer drugs
25I-NBOMe
25I-NBOH
MALDI MSI
dc.subject.br-rjbn.none.fl_str_mv subject.br-rjbn
description The phenethylamines derivatives, the NBOMes, N-bomb or Smiles, are potent hallucinogens, which are often sold as blotter paper. Changes in their molecular structures are constantly carried out, such as the exchange of halogen in the carbon 4 (C4) or the substitution of the methyl to a hydroxyl, observed in the modification of NBOMe to NBOH. This happens so that the new substances are not classified as illicit and preserved the psychoactive effects of molecules. In order to follow the dynamics of designer drugs market, the use of different analytical methods for the identification of these substances has been a solution. In this study, the matrix assisted laser desorption/ionization mass spectrometry (MALDI MS) and MALDI mass spectrometry imaging (MALDI MSI) were coupled to a Fourier transform ion cyclotron resonance mass spectrometer (FT-ICR MS) and used to analyze seven blotter papers of NBOMes containing 25I-NBOH (2-({[2-(4-iodo-2,5- dimethoxyphenyl) ethyl]amino}methyl) phenol, m/z 414,05) and 25I-NBOMe ((2-(4-iodo-2,5-dimethoxyphenyl)-N-[(2 methoxyphenyl) methyl]ethanamine), m/z 428,07). An optimization study was performed to evaluate the matrix application (pipette versus sprayer assisted by an ESI probe); the matrices (α-cyano-4-hydroxycinnamic acid (CHCA), 2,5 dihydroxybenzoic acid (DHB), 7,7,8,8-tetracyanoquinodimethane (TCNQ) and sinapinic acid (SA)) effect in the process of desorption and ionization and their concentration (from 5 to 25 mg.mL−1). After, a study of the spatial distribution of the NBOMes derivatives detected in the front and back of the blotter paper surface was performed. MALDI MS and MALDI MSI results showed that the matrix sprayer was the best method for matrix application, which allowed a homegeneous detection of the compound when compared to the pipette application. The CHCA matrix, in a concentration ≥ 15 mg.mL−1, displayed a higher ionization efficiency of the 25I-NBOMe compound, commonly detected in blotter paper, where an intense distribution was observed in relation to others matrices. The distribution of the active ingredient studied in the front and back between the six blotter papers analyzed showed that the three of them had a higher concentration of the active ingredient in only one of the sides (two in the back and one in the front), while the others presented a similar distribution in both sides.
publishDate 2020
dc.date.issued.fl_str_mv 2020-02-18
dc.date.accessioned.fl_str_mv 2024-05-30T00:49:48Z
dc.date.available.fl_str_mv 2024-05-30T00:49:48Z
dc.type.status.fl_str_mv info:eu-repo/semantics/publishedVersion
dc.type.driver.fl_str_mv info:eu-repo/semantics/masterThesis
format masterThesis
status_str publishedVersion
dc.identifier.uri.fl_str_mv http://repositorio.ufes.br/handle/10/15001
url http://repositorio.ufes.br/handle/10/15001
dc.language.iso.fl_str_mv por
language por
dc.rights.driver.fl_str_mv info:eu-repo/semantics/openAccess
eu_rights_str_mv openAccess
dc.format.none.fl_str_mv Text
dc.publisher.none.fl_str_mv Universidade Federal do Espírito Santo
Mestrado em Química
dc.publisher.program.fl_str_mv Programa de Pós-Graduação em Química
dc.publisher.initials.fl_str_mv UFES
dc.publisher.country.fl_str_mv BR
dc.publisher.department.fl_str_mv Centro de Ciências Exatas
publisher.none.fl_str_mv Universidade Federal do Espírito Santo
Mestrado em Química
dc.source.none.fl_str_mv reponame:Repositório Institucional da Universidade Federal do Espírito Santo (riUfes)
instname:Universidade Federal do Espírito Santo (UFES)
instacron:UFES
instname_str Universidade Federal do Espírito Santo (UFES)
instacron_str UFES
institution UFES
reponame_str Repositório Institucional da Universidade Federal do Espírito Santo (riUfes)
collection Repositório Institucional da Universidade Federal do Espírito Santo (riUfes)
bitstream.url.fl_str_mv http://repositorio.ufes.br/bitstreams/4602791f-7cb3-4007-a9e6-caef52a792b1/download
bitstream.checksum.fl_str_mv 7a9840acd8e997d25b5904613724feef
bitstream.checksumAlgorithm.fl_str_mv MD5
repository.name.fl_str_mv Repositório Institucional da Universidade Federal do Espírito Santo (riUfes) - Universidade Federal do Espírito Santo (UFES)
repository.mail.fl_str_mv riufes@ufes.br
_version_ 1856037481017769984