Plataformas alternativas para sistemas eletroforéticos integrados com detecção condutométrica sem contato
Autor(a) principal: | |
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Data de Publicação: | 2016 |
Tipo de documento: | Dissertação |
Idioma: | por |
Título da fonte: | Repositório Institucional da UFG |
Texto Completo: | http://repositorio.bc.ufg.br/tede/handle/tede/6332 |
Resumo: | This report describes the development of two alternative platforms for electrophoretic runs in microsystems. Firstly, the development of a hybrid capillary system that dispenses microfabrication steps is presented using fused silica capillaries interconnected by a commercial crossed shape interface. This hybrid system was coupled with contactless conductivity detector (C4D) to allow the determination of inorganic cations in biological samples. Electrokinetic sample injection was performed through gated mode approach for the first time in this arrangement. Operational parameters such as: (i) wave frequency and amplitude applied in C4D system, (ii) electrical potential applied in injection, (iii) injection time, (iv) detection point, (v) effect of capillary conditioning as well as and (vi) recovery percentage were extensively investigated and optimized. Better separations of cationic mixture containing NH4+, K+, Na+, Ca2+ and Mg2+ were achieved using a buffer system composed of 50 mM Lactic Acid, 20 mM Histidine and 3 mM 18-crown-6 on a capillary with effective length of 14.5 cm. . Addition of internal standard was used to ensure analytical reproducibility and allow the recording of merit figures. Linear behaviors were observed in concentration ranges between 10 and 100 M for NH4+, K+, Ca2+ e Mg2+, and 20-200 M for Na+. The limit of detection values calculated were 3.75 μM (NH4+), 3.70 μM (K+), 7.50 μM (Na+), 5.00 μM (Ca2+) and 5.35 μM (Mg2+). The concentration levels achieved for cations in biological samples ranged from 4,1 μM to 200 μM. Besides the hybrid system, this report also describes the development of an alternative methodology for the fabrication of high-relief masters for soft-lithography in poly(dimethylsiloxane) (PDMS) substrate. One of the innovative features makes reference to the use of low cost commercial photoresist from textile industry - poly(vinyl acetate) (PVAc) - which exhibits low toxicity. PVAc films were deposited on printed cirtuitry boards through the use of a homemade spincoater developed by desktop cooler, with rotation time control. This methodology allowed the production of high relief masters and PDMS channels with width and depth of 50 μm and 40 μm, respectively. Channels and masters profiles They were characterized with the following techniques: scan electron microscopy, perfilometry, optical and electrical. PDMS electrophoresis devices were successfully used for the separation of major inorganic cations. |
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Coltro, Wendell Karlos Tomazellihttp://lattes.cnpq.br/8302650734477213Coltro, Wendell Karlos Tomazellihttp://lattes.cnpq.br/8302650734477213Fonseca, AlexandreDuarte, Gabriela Rodrigues Mendeshttp://lattes.cnpq.br/7006713418517680Lobo Júnior, Eulício de Oliveira2016-10-03T14:18:22Z2016-03-10LOBO JÚNIOR, Eulício de Oliveira. Plataformas alternativas para sistemas eletroforéticos integrados com detecção condutométrica sem contato. 2016. 128 f. Dissertação (Mestrado em Química) - Universidade Federal de Goiás, Goiânia, 2016.http://repositorio.bc.ufg.br/tede/handle/tede/6332ark:/38995/001300000c9mjThis report describes the development of two alternative platforms for electrophoretic runs in microsystems. Firstly, the development of a hybrid capillary system that dispenses microfabrication steps is presented using fused silica capillaries interconnected by a commercial crossed shape interface. This hybrid system was coupled with contactless conductivity detector (C4D) to allow the determination of inorganic cations in biological samples. Electrokinetic sample injection was performed through gated mode approach for the first time in this arrangement. Operational parameters such as: (i) wave frequency and amplitude applied in C4D system, (ii) electrical potential applied in injection, (iii) injection time, (iv) detection point, (v) effect of capillary conditioning as well as and (vi) recovery percentage were extensively investigated and optimized. Better separations of cationic mixture containing NH4+, K+, Na+, Ca2+ and Mg2+ were achieved using a buffer system composed of 50 mM Lactic Acid, 20 mM Histidine and 3 mM 18-crown-6 on a capillary with effective length of 14.5 cm. . Addition of internal standard was used to ensure analytical reproducibility and allow the recording of merit figures. Linear behaviors were observed in concentration ranges between 10 and 100 M for NH4+, K+, Ca2+ e Mg2+, and 20-200 M for Na+. The limit of detection values calculated were 3.75 μM (NH4+), 3.70 μM (K+), 7.50 μM (Na+), 5.00 μM (Ca2+) and 5.35 μM (Mg2+). The concentration levels achieved for cations in biological samples ranged from 4,1 μM to 200 μM. Besides the hybrid system, this report also describes the development of an alternative methodology for the fabrication of high-relief masters for soft-lithography in poly(dimethylsiloxane) (PDMS) substrate. One of the innovative features makes reference to the use of low cost commercial photoresist from textile industry - poly(vinyl acetate) (PVAc) - which exhibits low toxicity. PVAc films were deposited on printed cirtuitry boards through the use of a homemade spincoater developed by desktop cooler, with rotation time control. This methodology allowed the production of high relief masters and PDMS channels with width and depth of 50 μm and 40 μm, respectively. Channels and masters profiles They were characterized with the following techniques: scan electron microscopy, perfilometry, optical and electrical. PDMS electrophoresis devices were successfully used for the separation of major inorganic cations.Esta dissertação descreve o desenvolvimento de duas plataformas alternativas para a realização de eletroforese em microssistemas. Inicialmente é descrita um sistema eletroforético híbrido que dispensa etapas de microfabricação utilizando capilares de sílica fundida, conectados por uma interface comercial com formato em cruz. Este sistema capilar híbrido foi acoplado com detecção condutométrica sem contato (C4D) e aplicado na determinação de cátions inorgânicos (NH4+, K+, Na+, Ca2+, Mg2+) em amostras biológicas. A injeção de amostras foi realizada eletrocineticamente no modo gated, sendo o primeiro estudo em capilares utilizando esta modalidade de injeção. Foram avaliados os parâmetros operacionais de funcionamento do sistema incluindo (i) frequência e amplitude da onda senoidal aplicada ao sistema de detecção, (ii) potencial elétrico aplicado na injeção, (iii) tempo de injeção, (iv) composição do tampão, (v) ponto de detecção, (vi) efeito do condicionamento do capilar e (vii) recuperação. As melhores separações para uma mistura contendo os cátions inorgânicos foram obtidas usando-se um sistema tamponante composto de ácido lático 50 mM, histidina 20 mM e éter coroa (18-crown-6) 3 mM em um capilar com comprimento efetivo de 14,5 cm. As figuras de mérito analítico foram obtidas a partir da adição do íon Li+ como padrão interno, o qual assegurou confiabilidade nas análises quantitativas. A partir da otimização dos parâmetros analíticos, as curvas analíticas para os íons NH4+, K+, Ca2+ e Mg2+ exibiram comportamento linear (R2>0,99) na faixa de 10-100 M enquanto a curva analítica para o íon Na+ proporcionou resposta linear na faixa de 20-200 M. Os limites de detecção encontrados para os cinco cátions foram entre 3,75 μM (NH4+), 3,75 μM (K+), 7,50 μM (Na+), 5,00 μM (Ca2+) e 5,35 μM (Mg2+). O sistema desenvolvido foi explorado para a determinação dos cátions inorgânicos em amostras de urina, saliva e lágrimas. As concentrações encontradas nas amostras biológicas variaram de 4,1 μM a 200 μM. Além do sistema híbrido, a dissertação também apresenta uma metodologia de baixo custo para produção de moldes em alto relevo para litografia suave em poli(dimetilsiloxano) (PDMS). A principal inovação é o uso de fotoresiste de baixo custo, que se trata de uma emulsão fotossensível de poli(acetato de vinila) (PVAc) utilizada na indústria têxtil e que apresenta baixa toxicidade. Outra inovação é o controle da altura dos moldes utilizando um spincoater de produção própria, com controle de tempo de rotação. Com esta metodologia foram produzidos moldes em alto relevo, e microchips em PDMS com 50 μm de largura e 40 μm de altura. Foram realizadas separações eletroforéticas dos cátions NH4+,K+,Na+,Ca2+,Mg2+e Li+. As eficiências de separação variaram entre 73.000 e 120.000 pratos/m. O que comprova que a metodologia alternativa apresenta aplicabilidade microfluídicaSubmitted by Jaqueline Silva (jtas29@gmail.com) on 2016-10-03T14:17:36Z No. of bitstreams: 2 Dissertação - Eunício de Oliveira Lobo Junior - 2016.pdf: 5628245 bytes, checksum: cb5cfdfdb21a0a9bed0292decf6c094f (MD5) license_rdf: 0 bytes, checksum: d41d8cd98f00b204e9800998ecf8427e (MD5)Approved for entry into archive by Jaqueline Silva (jtas29@gmail.com) on 2016-10-03T14:18:22Z (GMT) No. of bitstreams: 2 Dissertação - Eunício de Oliveira Lobo Junior - 2016.pdf: 5628245 bytes, checksum: cb5cfdfdb21a0a9bed0292decf6c094f (MD5) license_rdf: 0 bytes, checksum: d41d8cd98f00b204e9800998ecf8427e (MD5)Made available in DSpace on 2016-10-03T14:18:22Z (GMT). No. of bitstreams: 2 Dissertação - Eunício de Oliveira Lobo Junior - 2016.pdf: 5628245 bytes, checksum: cb5cfdfdb21a0a9bed0292decf6c094f (MD5) license_rdf: 0 bytes, checksum: d41d8cd98f00b204e9800998ecf8427e (MD5) Previous issue date: 2016-03-10Conselho Nacional de Pesquisa e Desenvolvimento Científico e Tecnológico - CNPqapplication/pdfporUniversidade Federal de GoiásPrograma de Pós-graduação em Química (IQ)UFGBrasilInstituto de Química - IQ (RG)http://creativecommons.org/licenses/by-nc-nd/4.0/info:eu-repo/semantics/openAccessEletroforese capilarMicrofluídicaDetecção condutométrica sem contatoMoldes em alto relevoPoli (dimetilsiloxano) PMDSCapillary electrophoresisMicrofluidicsContactless conductivity detectionHigh relief mastersPoly (dimethylsiloxane) PDMSQUIMICA::QUIMICA ANALITICAPlataformas alternativas para sistemas eletroforéticos integrados com detecção condutométrica sem contatoAlternative platforms for electrophoretic systems integrated with contactless conductivity detectioninfo:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/masterThesis6636939213254151586006006006007826066743741197278-8661602105461439549-2555911436985713659reponame:Repositório Institucional da UFGinstname:Universidade Federal de Goiás (UFG)instacron:UFGLICENSElicense.txtlicense.txttext/plain; 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dc.title.por.fl_str_mv |
Plataformas alternativas para sistemas eletroforéticos integrados com detecção condutométrica sem contato |
dc.title.alternative.eng.fl_str_mv |
Alternative platforms for electrophoretic systems integrated with contactless conductivity detection |
title |
Plataformas alternativas para sistemas eletroforéticos integrados com detecção condutométrica sem contato |
spellingShingle |
Plataformas alternativas para sistemas eletroforéticos integrados com detecção condutométrica sem contato Lobo Júnior, Eulício de Oliveira Eletroforese capilar Microfluídica Detecção condutométrica sem contato Moldes em alto relevo Poli (dimetilsiloxano) PMDS Capillary electrophoresis Microfluidics Contactless conductivity detection High relief masters Poly (dimethylsiloxane) PDMS QUIMICA::QUIMICA ANALITICA |
title_short |
Plataformas alternativas para sistemas eletroforéticos integrados com detecção condutométrica sem contato |
title_full |
Plataformas alternativas para sistemas eletroforéticos integrados com detecção condutométrica sem contato |
title_fullStr |
Plataformas alternativas para sistemas eletroforéticos integrados com detecção condutométrica sem contato |
title_full_unstemmed |
Plataformas alternativas para sistemas eletroforéticos integrados com detecção condutométrica sem contato |
title_sort |
Plataformas alternativas para sistemas eletroforéticos integrados com detecção condutométrica sem contato |
author |
Lobo Júnior, Eulício de Oliveira |
author_facet |
Lobo Júnior, Eulício de Oliveira |
author_role |
author |
dc.contributor.advisor1.fl_str_mv |
Coltro, Wendell Karlos Tomazelli |
dc.contributor.advisor1Lattes.fl_str_mv |
http://lattes.cnpq.br/8302650734477213 |
dc.contributor.referee1.fl_str_mv |
Coltro, Wendell Karlos Tomazelli |
dc.contributor.referee1Lattes.fl_str_mv |
http://lattes.cnpq.br/8302650734477213 |
dc.contributor.referee2.fl_str_mv |
Fonseca, Alexandre |
dc.contributor.referee3.fl_str_mv |
Duarte, Gabriela Rodrigues Mendes |
dc.contributor.authorLattes.fl_str_mv |
http://lattes.cnpq.br/7006713418517680 |
dc.contributor.author.fl_str_mv |
Lobo Júnior, Eulício de Oliveira |
contributor_str_mv |
Coltro, Wendell Karlos Tomazelli Coltro, Wendell Karlos Tomazelli Fonseca, Alexandre Duarte, Gabriela Rodrigues Mendes |
dc.subject.por.fl_str_mv |
Eletroforese capilar Microfluídica Detecção condutométrica sem contato Moldes em alto relevo Poli (dimetilsiloxano) PMDS |
topic |
Eletroforese capilar Microfluídica Detecção condutométrica sem contato Moldes em alto relevo Poli (dimetilsiloxano) PMDS Capillary electrophoresis Microfluidics Contactless conductivity detection High relief masters Poly (dimethylsiloxane) PDMS QUIMICA::QUIMICA ANALITICA |
dc.subject.eng.fl_str_mv |
Capillary electrophoresis Microfluidics Contactless conductivity detection High relief masters Poly (dimethylsiloxane) PDMS |
dc.subject.cnpq.fl_str_mv |
QUIMICA::QUIMICA ANALITICA |
description |
This report describes the development of two alternative platforms for electrophoretic runs in microsystems. Firstly, the development of a hybrid capillary system that dispenses microfabrication steps is presented using fused silica capillaries interconnected by a commercial crossed shape interface. This hybrid system was coupled with contactless conductivity detector (C4D) to allow the determination of inorganic cations in biological samples. Electrokinetic sample injection was performed through gated mode approach for the first time in this arrangement. Operational parameters such as: (i) wave frequency and amplitude applied in C4D system, (ii) electrical potential applied in injection, (iii) injection time, (iv) detection point, (v) effect of capillary conditioning as well as and (vi) recovery percentage were extensively investigated and optimized. Better separations of cationic mixture containing NH4+, K+, Na+, Ca2+ and Mg2+ were achieved using a buffer system composed of 50 mM Lactic Acid, 20 mM Histidine and 3 mM 18-crown-6 on a capillary with effective length of 14.5 cm. . Addition of internal standard was used to ensure analytical reproducibility and allow the recording of merit figures. Linear behaviors were observed in concentration ranges between 10 and 100 M for NH4+, K+, Ca2+ e Mg2+, and 20-200 M for Na+. The limit of detection values calculated were 3.75 μM (NH4+), 3.70 μM (K+), 7.50 μM (Na+), 5.00 μM (Ca2+) and 5.35 μM (Mg2+). The concentration levels achieved for cations in biological samples ranged from 4,1 μM to 200 μM. Besides the hybrid system, this report also describes the development of an alternative methodology for the fabrication of high-relief masters for soft-lithography in poly(dimethylsiloxane) (PDMS) substrate. One of the innovative features makes reference to the use of low cost commercial photoresist from textile industry - poly(vinyl acetate) (PVAc) - which exhibits low toxicity. PVAc films were deposited on printed cirtuitry boards through the use of a homemade spincoater developed by desktop cooler, with rotation time control. This methodology allowed the production of high relief masters and PDMS channels with width and depth of 50 μm and 40 μm, respectively. Channels and masters profiles They were characterized with the following techniques: scan electron microscopy, perfilometry, optical and electrical. PDMS electrophoresis devices were successfully used for the separation of major inorganic cations. |
publishDate |
2016 |
dc.date.accessioned.fl_str_mv |
2016-10-03T14:18:22Z |
dc.date.issued.fl_str_mv |
2016-03-10 |
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.citation.fl_str_mv |
LOBO JÚNIOR, Eulício de Oliveira. Plataformas alternativas para sistemas eletroforéticos integrados com detecção condutométrica sem contato. 2016. 128 f. Dissertação (Mestrado em Química) - Universidade Federal de Goiás, Goiânia, 2016. |
dc.identifier.uri.fl_str_mv |
http://repositorio.bc.ufg.br/tede/handle/tede/6332 |
dc.identifier.dark.fl_str_mv |
ark:/38995/001300000c9mj |
identifier_str_mv |
LOBO JÚNIOR, Eulício de Oliveira. Plataformas alternativas para sistemas eletroforéticos integrados com detecção condutométrica sem contato. 2016. 128 f. Dissertação (Mestrado em Química) - Universidade Federal de Goiás, Goiânia, 2016. ark:/38995/001300000c9mj |
url |
http://repositorio.bc.ufg.br/tede/handle/tede/6332 |
dc.language.iso.fl_str_mv |
por |
language |
por |
dc.relation.program.fl_str_mv |
663693921325415158 |
dc.relation.confidence.fl_str_mv |
600 600 600 600 |
dc.relation.department.fl_str_mv |
7826066743741197278 |
dc.relation.cnpq.fl_str_mv |
-8661602105461439549 |
dc.relation.sponsorship.fl_str_mv |
-2555911436985713659 |
dc.rights.driver.fl_str_mv |
http://creativecommons.org/licenses/by-nc-nd/4.0/ info:eu-repo/semantics/openAccess |
rights_invalid_str_mv |
http://creativecommons.org/licenses/by-nc-nd/4.0/ |
eu_rights_str_mv |
openAccess |
dc.format.none.fl_str_mv |
application/pdf |
dc.publisher.none.fl_str_mv |
Universidade Federal de Goiás |
dc.publisher.program.fl_str_mv |
Programa de Pós-graduação em Química (IQ) |
dc.publisher.initials.fl_str_mv |
UFG |
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Brasil |
dc.publisher.department.fl_str_mv |
Instituto de Química - IQ (RG) |
publisher.none.fl_str_mv |
Universidade Federal de Goiás |
dc.source.none.fl_str_mv |
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Universidade Federal de Goiás (UFG) |
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UFG |
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Repositório Institucional da UFG |
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Repositório Institucional da UFG |
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MD5 MD5 MD5 MD5 MD5 |
repository.name.fl_str_mv |
Repositório Institucional da UFG - Universidade Federal de Goiás (UFG) |
repository.mail.fl_str_mv |
tasesdissertacoes.bc@ufg.br |
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