Desenvolvimento de método para determinação de resíduos de medicamentos veterinários em salmão por UHPLC-MS/MS

Detalhes bibliográficos
Ano de defesa: 2019
Autor(a) principal: Bandeira, Nelson Miguel Grubel lattes
Orientador(a): Prestes, Osmar Damian lattes
Banca de defesa: Gonçalves, Fabio Ferreira lattes, Ballus, Cristiano Augusto lattes, Golombieski, Jaqueline Ineu lattes, Cabrera, Liziara da Costa lattes
Tipo de documento: Tese
Tipo de acesso: Acesso aberto
Idioma: por
Instituição de defesa: Universidade Federal de Santa Maria
Centro de Ciências Naturais e Exatas
Programa de Pós-Graduação: Programa de Pós-Graduação em Química
Departamento: Química
País: Brasil
Palavras-chave em Português:
Palavras-chave em Inglês:
Área do conhecimento CNPq:
Link de acesso: http://repositorio.ufsm.br/handle/1/19389
Resumo: The aquaculture industry has been growing, developing and highlightning in the last few years. Many countries and international organizations have invested in developing the activity according to available resources. Chile stands out in the world market in salmon production (Salmo salar) being the main supplier of the product to Brazil. Veterinary drugs may be used during the production process for the proper management and prevention of financial losses. Once administered, veterinary drugs can be absorbed and remain in fish meat as residues. Many drugs are banned for veterinary use, many others are authorized and require application, attendance and appropriate withdrawal period to not leave residues in the product. The presence of drug residues is of great concern, since small doses given daily can lead to the development of bacterial resistance. Monitoring of the presence of residues can be carried out through programs and regulations. The presence of residues of veterinary drugs in products of animal origin is determined by reliable and suitable analytical methods. Therefore, the objective of this work was to develop an analytical method for the determination of residues of nitroimidazoles, quinolones, tetracyclines, amphenicoles, sulfonamides, macrolides, pyrethroids and benzamides in salmon (Salmo salar) using UHPLC-MS/MS. The development of the method was performed by assays for evaluation of the solvents used in the extraction and sorbents used in the sample preparation step. The conditions of the UHPLC-MS/MS system, such as mobile fase composition, chromatographic column, mobile phase elution gradient, mobile phase flow rate, desolvation gas temperature and tension applied to the capillary were also evaluated. The method of sample preparation was based on the extraction with acetonitrile and clean up step using SPE. The determination step was performed in UHPLC-MS/MS Xevo TQ® system. The mobile phase used was aqueous solution and acetonitrile, both 0.1% formic acid (v/v) at the flow rate of 0.1 mL min-1 in gradient mode. The chromatographic column used was an Acquity HSST3 (50 x 2.1 mm, 1.8 μm) at 60 ° C. The injection volume was 10 μL. The conditions of the ionization source (ESI) were desolvation gas temperature of 600 °C, capillary voltage of 2000 V, source temperature 150 °C. The validation of the method developed was based on documents CD/657/EU and SANTE, 2017. The results of recovery varied between 71 and 120% with deviations less than 24%. The quantification limits ranged from 5 to 25 μg kg-1 . Matrix effects were mostly negative ranging from -45 to -22%. The method was applied in the analysis of 15 real samples. The method is suitable for the determination of residues of veterinary drugs in routine laboratories for 5 of the classes under study within the limits established by the legislation.
id UFSM_a6c812a086b3bfbcb4f51951fb84b5b8
oai_identifier_str oai:repositorio.ufsm.br:1/19389
network_acronym_str UFSM
network_name_str Biblioteca Digital de Teses e Dissertações do UFSM
repository_id_str
spelling 2020-01-20T11:22:34Z2020-01-20T11:22:34Z2019-02-27http://repositorio.ufsm.br/handle/1/19389The aquaculture industry has been growing, developing and highlightning in the last few years. Many countries and international organizations have invested in developing the activity according to available resources. Chile stands out in the world market in salmon production (Salmo salar) being the main supplier of the product to Brazil. Veterinary drugs may be used during the production process for the proper management and prevention of financial losses. Once administered, veterinary drugs can be absorbed and remain in fish meat as residues. Many drugs are banned for veterinary use, many others are authorized and require application, attendance and appropriate withdrawal period to not leave residues in the product. The presence of drug residues is of great concern, since small doses given daily can lead to the development of bacterial resistance. Monitoring of the presence of residues can be carried out through programs and regulations. The presence of residues of veterinary drugs in products of animal origin is determined by reliable and suitable analytical methods. Therefore, the objective of this work was to develop an analytical method for the determination of residues of nitroimidazoles, quinolones, tetracyclines, amphenicoles, sulfonamides, macrolides, pyrethroids and benzamides in salmon (Salmo salar) using UHPLC-MS/MS. The development of the method was performed by assays for evaluation of the solvents used in the extraction and sorbents used in the sample preparation step. The conditions of the UHPLC-MS/MS system, such as mobile fase composition, chromatographic column, mobile phase elution gradient, mobile phase flow rate, desolvation gas temperature and tension applied to the capillary were also evaluated. The method of sample preparation was based on the extraction with acetonitrile and clean up step using SPE. The determination step was performed in UHPLC-MS/MS Xevo TQ® system. The mobile phase used was aqueous solution and acetonitrile, both 0.1% formic acid (v/v) at the flow rate of 0.1 mL min-1 in gradient mode. The chromatographic column used was an Acquity HSST3 (50 x 2.1 mm, 1.8 μm) at 60 ° C. The injection volume was 10 μL. The conditions of the ionization source (ESI) were desolvation gas temperature of 600 °C, capillary voltage of 2000 V, source temperature 150 °C. The validation of the method developed was based on documents CD/657/EU and SANTE, 2017. The results of recovery varied between 71 and 120% with deviations less than 24%. The quantification limits ranged from 5 to 25 μg kg-1 . Matrix effects were mostly negative ranging from -45 to -22%. The method was applied in the analysis of 15 real samples. The method is suitable for the determination of residues of veterinary drugs in routine laboratories for 5 of the classes under study within the limits established by the legislation.A indústria aquícola vem crescendo, se desenvolvendo e se destacando ao longo dos ultimos anos. Muitos países e organizações internacionais tem investido no desenvolvimento da atividade de acordo com os recursos disponíveis. O Chile se destaca no mercado mundial no que diz respeito a produção de salmão (Salmo salar) sendo principal fornecedor do produto para o Brasil. Os medicamentos veterinários podem ser utilizados durante o processo produtivo visando o manejo adequado e a prevenção de prejuízos financeiros. Uma vez administrados, os medicamentos veterinários podem ser absorvidos e permanecer na carne dos peixes na forma de resíduo. Muitos medicamentos são proíbidos para uso veterinário, muitos outros são autorizados e exigem aplicação, acompanhamento e período de carência adequado para não deixar resíduos no produto final. A prensença de resíduos de medicamentos é de grande preocupação uma vez que pequenas doses, administradas diariamente, podem levar ao desenvolvimento de resistência bacteriana. O monitoramento da presença de resíduos pode ser realizado através de programas e regulamentações. A determinação da presença de resíduos de medicamentos veterinários em produtos de origem animal é realizada através de métodos analíticos seguros e confiáveis. Portanto, o objetivo deste trabalho foi desenvolver um método analítico para determinação de resíduos de nitroimidazóis, quinolonas, tetraciclinas, anfenicóis, sulfonamidas, macrolídeos, piretróides e benzamidas em salmão (Salmo salar) utilizando UHPLC-MS/MS. Para desenvolvimento do método ensaios para avaliação dos solventes utilizados na extração e sorventes utilizados na etapa de preparo de amostra foram realizados. As condições do sistema UHPLC-MS/MS, como composição da faz móvel, coluna de separação, gradiente de eluição da fase móvel, vazão da fase móvel, temperatura do gas de dessolvatação e tensão aplicada ao capilar também foram avaliadas. O método teve como etapa de preparo de amostra extração com acetonitrila e limpeza de extrato utilizando SPE. A etapa de determinação foi realizada em sistema UHPOLC-MS/MS Xevo TQ®. A fase móvel utilizada foi solução aquosa e acetonitrila, ambos 0,1% ácido fórmico (v/v) na vazão de 100 µL min-1no modo gradiente. A coluna cromatográfica utilizada foi uma Acquity HSST3 ( 50 x 2,1 mm, 1,8 µm) à 60 °C. O volume de injeção foi de 10 µL. As condições da fonte de ionização (ESI) foram temperatura do gás de dessolvatação de 600 °C, tensão do capilar de 2000 V, temperatura da fonte 150 °C. A validação do método desenvolvido foi realizada com base nos documento CD/657/EU e SANTE, 2017. Os resultados de recuperação variaram entre 71 e 120% com desvios menores do que 24%. Os limites de quantificação alcançados variaram entre 5 e 25 µg kg-1 . Efeitos de matriz foram em sua maioria negativos variando entre -45 e -22%. O método foi aplicado na análise de 15 amostras reais. O método é adequado para a determinação de resíduos de medicamentos veterinários em laboratórios de rotina para 5 das classes em estudo dentro dos limites estabelecidos pela legislação.Coordenação de Aperfeiçoamento de Pessoal de Nível Superior - CAPESporUniversidade Federal de Santa MariaCentro de Ciências Naturais e ExatasPrograma de Pós-Graduação em QuímicaUFSMBrasilQuímicaAttribution-NonCommercial-NoDerivatives 4.0 Internationalhttp://creativecommons.org/licenses/by-nc-nd/4.0/info:eu-repo/semantics/openAccessPlanejamento de experimentosAquiculturaExtração sólido líquidoDesign of experimentsAquacultureSolid liquid extractionCNPQ::CIENCIAS EXATAS E DA TERRA::QUIMICADesenvolvimento de método para determinação de resíduos de medicamentos veterinários em salmão por UHPLC-MS/MSDevelopment of method for determination of veterinary drug residues in salmon by UHPLC-MS/MSinfo:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/doctoralThesisPrestes, Osmar Damianhttp://lattes.cnpq.br/9632234955509028Gonçalves, Fabio Ferreirahttp://lattes.cnpq.br/1090108357021843Ballus, Cristiano Augustohttp://lattes.cnpq.br/5141003597392061Golombieski, Jaqueline Ineuhttp://lattes.cnpq.br/0884818333843539Cabrera, Liziara da Costahttp://lattes.cnpq.br/2380427486727653http://lattes.cnpq.br/3270700108583990Bandeira, Nelson Miguel Grubel100600000000600f79cc0c9-c923-4244-9c1f-c80d7467441045a3bd9e-8b4a-43b4-ae3e-f73d94374d509e2a8b3c-033e-4402-a719-b5bd327df04b8aed6c33-9c7e-40d6-9fe2-fd5138d70219c7500b83-c922-42a2-baf1-698480cb4a486916a2fc-d593-49ec-bec1-09db8246173ereponame:Biblioteca Digital de Teses e Dissertações do UFSMinstname:Universidade Federal de Santa Maria (UFSM)instacron:UFSMORIGINALTES_PPGQUIMICA_2019_BANDEIRA_NELSON.pdfTES_PPGQUIMICA_2019_BANDEIRA_NELSON.pdfTese de Doutoradoapplication/pdf11050330http://repositorio.ufsm.br/bitstream/1/19389/1/TES_PPGQUIMICA_2019_BANDEIRA_NELSON.pdf064845c0e5c5f0fbaf95b1c327605efbMD51CC-LICENSElicense_rdflicense_rdfapplication/rdf+xml; charset=utf-8805http://repositorio.ufsm.br/bitstream/1/19389/2/license_rdf4460e5956bc1d1639be9ae6146a50347MD52LICENSElicense.txtlicense.txttext/plain; charset=utf-81956http://repositorio.ufsm.br/bitstream/1/19389/3/license.txt2f0571ecee68693bd5cd3f17c1e075dfMD53TEXTTES_PPGQUIMICA_2019_BANDEIRA_NELSON.pdf.txtTES_PPGQUIMICA_2019_BANDEIRA_NELSON.pdf.txtExtracted texttext/plain281191http://repositorio.ufsm.br/bitstream/1/19389/4/TES_PPGQUIMICA_2019_BANDEIRA_NELSON.pdf.txtc6b2ec0b0210ef52afd88ee82c836063MD54THUMBNAILTES_PPGQUIMICA_2019_BANDEIRA_NELSON.pdf.jpgTES_PPGQUIMICA_2019_BANDEIRA_NELSON.pdf.jpgIM Thumbnailimage/jpeg4380http://repositorio.ufsm.br/bitstream/1/19389/5/TES_PPGQUIMICA_2019_BANDEIRA_NELSON.pdf.jpg9a4f270f923857cf468c861b780be922MD551/193892020-01-21 03:03:11.943oai:repositorio.ufsm.br:1/19389TElDRU7Dh0EgREUgRElTVFJJQlVJw4fDg08gTsODTy1FWENMVVNJVkEKCkNvbSBhIGFwcmVzZW50YcOnw6NvIGRlc3RhIGxpY2Vuw6dhLCB2b2PDqiAobyBhdXRvciAoZXMpIG91IG8gdGl0dWxhciBkb3MgZGlyZWl0b3MgZGUgYXV0b3IpIGNvbmNlZGUgw6AgVW5pdmVyc2lkYWRlCkZlZGVyYWwgZGUgU2FudGEgTWFyaWEgKFVGU00pIG8gZGlyZWl0byBuw6NvLWV4Y2x1c2l2byBkZSByZXByb2R1emlyLCAgdHJhZHV6aXIgKGNvbmZvcm1lIGRlZmluaWRvIGFiYWl4byksIGUvb3UKZGlzdHJpYnVpciBhIHN1YSB0ZXNlIG91IGRpc3NlcnRhw6fDo28gKGluY2x1aW5kbyBvIHJlc3VtbykgcG9yIHRvZG8gbyBtdW5kbyBubyBmb3JtYXRvIGltcHJlc3NvIGUgZWxldHLDtG5pY28gZQplbSBxdWFscXVlciBtZWlvLCBpbmNsdWluZG8gb3MgZm9ybWF0b3Mgw6F1ZGlvIG91IHbDrWRlby4KClZvY8OqIGNvbmNvcmRhIHF1ZSBhIFVGU00gcG9kZSwgc2VtIGFsdGVyYXIgbyBjb250ZcO6ZG8sIHRyYW5zcG9yIGEgc3VhIHRlc2Ugb3UgZGlzc2VydGHDp8OjbwpwYXJhIHF1YWxxdWVyIG1laW8gb3UgZm9ybWF0byBwYXJhIGZpbnMgZGUgcHJlc2VydmHDp8Ojby4KClZvY8OqIHRhbWLDqW0gY29uY29yZGEgcXVlIGEgVUZTTSBwb2RlIG1hbnRlciBtYWlzIGRlIHVtYSBjw7NwaWEgYSBzdWEgdGVzZSBvdQpkaXNzZXJ0YcOnw6NvIHBhcmEgZmlucyBkZSBzZWd1cmFuw6dhLCBiYWNrLXVwIGUgcHJlc2VydmHDp8Ojby4KClZvY8OqIGRlY2xhcmEgcXVlIGEgc3VhIHRlc2Ugb3UgZGlzc2VydGHDp8OjbyDDqSBvcmlnaW5hbCBlIHF1ZSB2b2PDqiB0ZW0gbyBwb2RlciBkZSBjb25jZWRlciBvcyBkaXJlaXRvcyBjb250aWRvcwpuZXN0YSBsaWNlbsOnYS4gVm9jw6ogdGFtYsOpbSBkZWNsYXJhIHF1ZSBvIGRlcMOzc2l0byBkYSBzdWEgdGVzZSBvdSBkaXNzZXJ0YcOnw6NvIG7Do28sIHF1ZSBzZWphIGRlIHNldQpjb25oZWNpbWVudG8sIGluZnJpbmdlIGRpcmVpdG9zIGF1dG9yYWlzIGRlIG5pbmd1w6ltLgoKQ2FzbyBhIHN1YSB0ZXNlIG91IGRpc3NlcnRhw6fDo28gY29udGVuaGEgbWF0ZXJpYWwgcXVlIHZvY8OqIG7Do28gcG9zc3VpIGEgdGl0dWxhcmlkYWRlIGRvcyBkaXJlaXRvcyBhdXRvcmFpcywgdm9jw6oKZGVjbGFyYSBxdWUgb2J0ZXZlIGEgcGVybWlzc8OjbyBpcnJlc3RyaXRhIGRvIGRldGVudG9yIGRvcyBkaXJlaXRvcyBhdXRvcmFpcyBwYXJhIGNvbmNlZGVyIMOgIFVGU00Kb3MgZGlyZWl0b3MgYXByZXNlbnRhZG9zIG5lc3RhIGxpY2Vuw6dhLCBlIHF1ZSBlc3NlIG1hdGVyaWFsIGRlIHByb3ByaWVkYWRlIGRlIHRlcmNlaXJvcyBlc3TDoSBjbGFyYW1lbnRlCmlkZW50aWZpY2FkbyBlIHJlY29uaGVjaWRvIG5vIHRleHRvIG91IG5vIGNvbnRlw7pkbyBkYSB0ZXNlIG91IGRpc3NlcnRhw6fDo28gb3JhIGRlcG9zaXRhZGEuCgpDQVNPIEEgVEVTRSBPVSBESVNTRVJUQcOHw4NPIE9SQSBERVBPU0lUQURBIFRFTkhBIFNJRE8gUkVTVUxUQURPIERFIFVNIFBBVFJPQ8ONTklPIE9VCkFQT0lPIERFIFVNQSBBR8OKTkNJQSBERSBGT01FTlRPIE9VIE9VVFJPIE9SR0FOSVNNTyBRVUUgTsODTyBTRUpBIEEgVUZTTQosIFZPQ8OKIERFQ0xBUkEgUVVFIFJFU1BFSVRPVSBUT0RPUyBFIFFVQUlTUVVFUiBESVJFSVRPUyBERSBSRVZJU8ODTyBDT01PClRBTULDiU0gQVMgREVNQUlTIE9CUklHQcOHw5VFUyBFWElHSURBUyBQT1IgQ09OVFJBVE8gT1UgQUNPUkRPLgoKQSBVRlNNIHNlIGNvbXByb21ldGUgYSBpZGVudGlmaWNhciBjbGFyYW1lbnRlIG8gc2V1IG5vbWUgKHMpIG91IG8ocykgbm9tZShzKSBkbyhzKQpkZXRlbnRvcihlcykgZG9zIGRpcmVpdG9zIGF1dG9yYWlzIGRhIHRlc2Ugb3UgZGlzc2VydGHDp8OjbywgZSBuw6NvIGZhcsOhIHF1YWxxdWVyIGFsdGVyYcOnw6NvLCBhbMOpbSBkYXF1ZWxhcwpjb25jZWRpZGFzIHBvciBlc3RhIGxpY2Vuw6dhLgoKBiblioteca Digital de Teses e Dissertaçõeshttps://repositorio.ufsm.br/ONGhttps://repositorio.ufsm.br/oai/requestatendimento.sib@ufsm.br||tedebc@gmail.comopendoar:2020-01-21T06:03:11Biblioteca Digital de Teses e Dissertações do UFSM - Universidade Federal de Santa Maria (UFSM)false
dc.title.por.fl_str_mv Desenvolvimento de método para determinação de resíduos de medicamentos veterinários em salmão por UHPLC-MS/MS
dc.title.alternative.eng.fl_str_mv Development of method for determination of veterinary drug residues in salmon by UHPLC-MS/MS
title Desenvolvimento de método para determinação de resíduos de medicamentos veterinários em salmão por UHPLC-MS/MS
spellingShingle Desenvolvimento de método para determinação de resíduos de medicamentos veterinários em salmão por UHPLC-MS/MS
Bandeira, Nelson Miguel Grubel
Planejamento de experimentos
Aquicultura
Extração sólido líquido
Design of experiments
Aquaculture
Solid liquid extraction
CNPQ::CIENCIAS EXATAS E DA TERRA::QUIMICA
title_short Desenvolvimento de método para determinação de resíduos de medicamentos veterinários em salmão por UHPLC-MS/MS
title_full Desenvolvimento de método para determinação de resíduos de medicamentos veterinários em salmão por UHPLC-MS/MS
title_fullStr Desenvolvimento de método para determinação de resíduos de medicamentos veterinários em salmão por UHPLC-MS/MS
title_full_unstemmed Desenvolvimento de método para determinação de resíduos de medicamentos veterinários em salmão por UHPLC-MS/MS
title_sort Desenvolvimento de método para determinação de resíduos de medicamentos veterinários em salmão por UHPLC-MS/MS
author Bandeira, Nelson Miguel Grubel
author_facet Bandeira, Nelson Miguel Grubel
author_role author
dc.contributor.advisor1.fl_str_mv Prestes, Osmar Damian
dc.contributor.advisor1Lattes.fl_str_mv http://lattes.cnpq.br/9632234955509028
dc.contributor.referee1.fl_str_mv Gonçalves, Fabio Ferreira
dc.contributor.referee1Lattes.fl_str_mv http://lattes.cnpq.br/1090108357021843
dc.contributor.referee2.fl_str_mv Ballus, Cristiano Augusto
dc.contributor.referee2Lattes.fl_str_mv http://lattes.cnpq.br/5141003597392061
dc.contributor.referee3.fl_str_mv Golombieski, Jaqueline Ineu
dc.contributor.referee3Lattes.fl_str_mv http://lattes.cnpq.br/0884818333843539
dc.contributor.referee4.fl_str_mv Cabrera, Liziara da Costa
dc.contributor.referee4Lattes.fl_str_mv http://lattes.cnpq.br/2380427486727653
dc.contributor.authorLattes.fl_str_mv http://lattes.cnpq.br/3270700108583990
dc.contributor.author.fl_str_mv Bandeira, Nelson Miguel Grubel
contributor_str_mv Prestes, Osmar Damian
Gonçalves, Fabio Ferreira
Ballus, Cristiano Augusto
Golombieski, Jaqueline Ineu
Cabrera, Liziara da Costa
dc.subject.por.fl_str_mv Planejamento de experimentos
Aquicultura
Extração sólido líquido
topic Planejamento de experimentos
Aquicultura
Extração sólido líquido
Design of experiments
Aquaculture
Solid liquid extraction
CNPQ::CIENCIAS EXATAS E DA TERRA::QUIMICA
dc.subject.eng.fl_str_mv Design of experiments
Aquaculture
Solid liquid extraction
dc.subject.cnpq.fl_str_mv CNPQ::CIENCIAS EXATAS E DA TERRA::QUIMICA
description The aquaculture industry has been growing, developing and highlightning in the last few years. Many countries and international organizations have invested in developing the activity according to available resources. Chile stands out in the world market in salmon production (Salmo salar) being the main supplier of the product to Brazil. Veterinary drugs may be used during the production process for the proper management and prevention of financial losses. Once administered, veterinary drugs can be absorbed and remain in fish meat as residues. Many drugs are banned for veterinary use, many others are authorized and require application, attendance and appropriate withdrawal period to not leave residues in the product. The presence of drug residues is of great concern, since small doses given daily can lead to the development of bacterial resistance. Monitoring of the presence of residues can be carried out through programs and regulations. The presence of residues of veterinary drugs in products of animal origin is determined by reliable and suitable analytical methods. Therefore, the objective of this work was to develop an analytical method for the determination of residues of nitroimidazoles, quinolones, tetracyclines, amphenicoles, sulfonamides, macrolides, pyrethroids and benzamides in salmon (Salmo salar) using UHPLC-MS/MS. The development of the method was performed by assays for evaluation of the solvents used in the extraction and sorbents used in the sample preparation step. The conditions of the UHPLC-MS/MS system, such as mobile fase composition, chromatographic column, mobile phase elution gradient, mobile phase flow rate, desolvation gas temperature and tension applied to the capillary were also evaluated. The method of sample preparation was based on the extraction with acetonitrile and clean up step using SPE. The determination step was performed in UHPLC-MS/MS Xevo TQ® system. The mobile phase used was aqueous solution and acetonitrile, both 0.1% formic acid (v/v) at the flow rate of 0.1 mL min-1 in gradient mode. The chromatographic column used was an Acquity HSST3 (50 x 2.1 mm, 1.8 μm) at 60 ° C. The injection volume was 10 μL. The conditions of the ionization source (ESI) were desolvation gas temperature of 600 °C, capillary voltage of 2000 V, source temperature 150 °C. The validation of the method developed was based on documents CD/657/EU and SANTE, 2017. The results of recovery varied between 71 and 120% with deviations less than 24%. The quantification limits ranged from 5 to 25 μg kg-1 . Matrix effects were mostly negative ranging from -45 to -22%. The method was applied in the analysis of 15 real samples. The method is suitable for the determination of residues of veterinary drugs in routine laboratories for 5 of the classes under study within the limits established by the legislation.
publishDate 2019
dc.date.issued.fl_str_mv 2019-02-27
dc.date.accessioned.fl_str_mv 2020-01-20T11:22:34Z
dc.date.available.fl_str_mv 2020-01-20T11:22:34Z
dc.type.status.fl_str_mv info:eu-repo/semantics/publishedVersion
dc.type.driver.fl_str_mv info:eu-repo/semantics/doctoralThesis
format doctoralThesis
status_str publishedVersion
dc.identifier.uri.fl_str_mv http://repositorio.ufsm.br/handle/1/19389
url http://repositorio.ufsm.br/handle/1/19389
dc.language.iso.fl_str_mv por
language por
dc.relation.cnpq.fl_str_mv 100600000000
dc.relation.confidence.fl_str_mv 600
dc.relation.authority.fl_str_mv f79cc0c9-c923-4244-9c1f-c80d74674410
45a3bd9e-8b4a-43b4-ae3e-f73d94374d50
9e2a8b3c-033e-4402-a719-b5bd327df04b
8aed6c33-9c7e-40d6-9fe2-fd5138d70219
c7500b83-c922-42a2-baf1-698480cb4a48
6916a2fc-d593-49ec-bec1-09db8246173e
dc.rights.driver.fl_str_mv Attribution-NonCommercial-NoDerivatives 4.0 International
http://creativecommons.org/licenses/by-nc-nd/4.0/
info:eu-repo/semantics/openAccess
rights_invalid_str_mv Attribution-NonCommercial-NoDerivatives 4.0 International
http://creativecommons.org/licenses/by-nc-nd/4.0/
eu_rights_str_mv openAccess
dc.publisher.none.fl_str_mv Universidade Federal de Santa Maria
Centro de Ciências Naturais e Exatas
dc.publisher.program.fl_str_mv Programa de Pós-Graduação em Química
dc.publisher.initials.fl_str_mv UFSM
dc.publisher.country.fl_str_mv Brasil
dc.publisher.department.fl_str_mv Química
publisher.none.fl_str_mv Universidade Federal de Santa Maria
Centro de Ciências Naturais e Exatas
dc.source.none.fl_str_mv reponame:Biblioteca Digital de Teses e Dissertações do UFSM
instname:Universidade Federal de Santa Maria (UFSM)
instacron:UFSM
instname_str Universidade Federal de Santa Maria (UFSM)
instacron_str UFSM
institution UFSM
reponame_str Biblioteca Digital de Teses e Dissertações do UFSM
collection Biblioteca Digital de Teses e Dissertações do UFSM
bitstream.url.fl_str_mv http://repositorio.ufsm.br/bitstream/1/19389/1/TES_PPGQUIMICA_2019_BANDEIRA_NELSON.pdf
http://repositorio.ufsm.br/bitstream/1/19389/2/license_rdf
http://repositorio.ufsm.br/bitstream/1/19389/3/license.txt
http://repositorio.ufsm.br/bitstream/1/19389/4/TES_PPGQUIMICA_2019_BANDEIRA_NELSON.pdf.txt
http://repositorio.ufsm.br/bitstream/1/19389/5/TES_PPGQUIMICA_2019_BANDEIRA_NELSON.pdf.jpg
bitstream.checksum.fl_str_mv 064845c0e5c5f0fbaf95b1c327605efb
4460e5956bc1d1639be9ae6146a50347
2f0571ecee68693bd5cd3f17c1e075df
c6b2ec0b0210ef52afd88ee82c836063
9a4f270f923857cf468c861b780be922
bitstream.checksumAlgorithm.fl_str_mv MD5
MD5
MD5
MD5
MD5
repository.name.fl_str_mv Biblioteca Digital de Teses e Dissertações do UFSM - Universidade Federal de Santa Maria (UFSM)
repository.mail.fl_str_mv atendimento.sib@ufsm.br||tedebc@gmail.com
_version_ 1793240114310152192