Desenvolvimento de método de preparo de amostras de solução de nutrição enteral mediante sistema de digestão de alta pressão para posterior determinação multielementar

Detalhes bibliográficos
Ano de defesa: 2018
Autor(a) principal: Anschau, Kéllen Francine lattes
Orientador(a): Muller, Edson Irineu lattes
Banca de defesa: Pozebon, Dirce lattes, Duarte, Fábio Andrei lattes
Tipo de documento: Dissertação
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/1/18684
Resumo: In this work two methods of sample preparation for the digestion of enteral nutrition solution (SNE) using microwave assisted digestion (MWAD) in a single reaction chamber (SRC) system and subsequent multielement determination by plasma-based techniques (ICP OES and ICP-MS) were evaluated. For H2O2, parameters such as H2O2 concentration (30, 40 and 50%), temperature of the SRC system (190, 230 and 250 ° C), volume of H2O2 (6, 8 and 10 mL) and the sample mass (ranging from 250 mg to 1500 mg) were investigated. The evaluation of the best condition was made based on the concentration of residual C and the residual acidity of the digests. The best condition for the SRC system with H2O2 was 8 mL of 50% H2O2, temperature of 250 ° C and mass of 1000 mg of SNE. In this condition, the residual C concentration obtained was 711 mg L-1 and negligible residual acidity. Subsequently, the best condition obtained with H2O2 was also applied to concentrated HNO3. Using concentrated HNO3, a residual C concentration of 123 mg L-1 and a high residual acidity (7,7 mol L-1 of HNO3) were obtained. In addition, the decomposition efficiency of the components of the SNE formulation were evaluated. For this, sodium caseinate, glucose syrup and sunflower and canola oils were digested using 8 mL of 50% H2O2. It was observed that sodium caseinate and sunflower and canola oils had the highest values of residual carbon. In addition, wet digestion of refractory organic compounds such as histidine, tryptophan, phenylalanine and linoleic acid was performed using the SRC system with 50% H2O2 and concentrated HNO3. The values of residual carbon content (RCC) obtained for these refractory organic substances were significantly lower than reported in the literature, probably due to the more drastic pressure and temperature conditions allowed by the SRC system. Finally, the determination of As, Ca, Cd, Co, Cr, Cu, Fe, K, Mg, Mn, Mo, Na, P, Pb, Se and Zn were performed by ICP OES and ICP-MS and were not observed significant differences between the results obtained by the methods that used 50% H2O2 and concentrated HNO3. The accuracy was also evaluated with a reference material (NIST 8435 Whole Milk Powder).
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spelling 2019-10-25T18:27:58Z2019-10-25T18:27:58Z2018-03-01http://repositorio.ufsm.br/handle/1/18684In this work two methods of sample preparation for the digestion of enteral nutrition solution (SNE) using microwave assisted digestion (MWAD) in a single reaction chamber (SRC) system and subsequent multielement determination by plasma-based techniques (ICP OES and ICP-MS) were evaluated. For H2O2, parameters such as H2O2 concentration (30, 40 and 50%), temperature of the SRC system (190, 230 and 250 ° C), volume of H2O2 (6, 8 and 10 mL) and the sample mass (ranging from 250 mg to 1500 mg) were investigated. The evaluation of the best condition was made based on the concentration of residual C and the residual acidity of the digests. The best condition for the SRC system with H2O2 was 8 mL of 50% H2O2, temperature of 250 ° C and mass of 1000 mg of SNE. In this condition, the residual C concentration obtained was 711 mg L-1 and negligible residual acidity. Subsequently, the best condition obtained with H2O2 was also applied to concentrated HNO3. Using concentrated HNO3, a residual C concentration of 123 mg L-1 and a high residual acidity (7,7 mol L-1 of HNO3) were obtained. In addition, the decomposition efficiency of the components of the SNE formulation were evaluated. For this, sodium caseinate, glucose syrup and sunflower and canola oils were digested using 8 mL of 50% H2O2. It was observed that sodium caseinate and sunflower and canola oils had the highest values of residual carbon. In addition, wet digestion of refractory organic compounds such as histidine, tryptophan, phenylalanine and linoleic acid was performed using the SRC system with 50% H2O2 and concentrated HNO3. The values of residual carbon content (RCC) obtained for these refractory organic substances were significantly lower than reported in the literature, probably due to the more drastic pressure and temperature conditions allowed by the SRC system. Finally, the determination of As, Ca, Cd, Co, Cr, Cu, Fe, K, Mg, Mn, Mo, Na, P, Pb, Se and Zn were performed by ICP OES and ICP-MS and were not observed significant differences between the results obtained by the methods that used 50% H2O2 and concentrated HNO3. The accuracy was also evaluated with a reference material (NIST 8435 Whole Milk Powder).Neste trabalho foram desenvolvidos dois métodos de decomposição de amostra de solução de nutrição enteral (SNE), empregando decomposição assistida por radiação micro-ondas (MWAD) em sistema de câmara única de reação (SRC) com subsequente determinação multielementar pelas técnicas de espectrometria de emissão óptica com plasma indutivamente acoplado (ICP OES) e espectrometria de massa com plasma indutivamente acoplado (ICP-MS). Foram avaliados a concentração de H2O2 (30, 40 e 50% v/v), a temperatura de aquecimento do sistema SRC (190, 230 e 250 °C), o volume de H2O2 (6, 8 e 10 mL) e a massa de amostra (250, 500, 750, 1000 e 1500 mg). A avaliação da melhor condição foi feita a partir dos resultados da concentração de C residual e acidez nos digeridos. A melhor condição para o sistema SRC com H2O2 foi de 8 mL de H2O2 50% v/v, temperatura de 250 °C e massa de 1000 mg de SNE. Nessa condição, a concentração de C residual obtida foi 711 mg L-1 e a acidez residual desprezível. Posteriormente, nessas condições o H2O2, foi substituído pelo HNO3 concentrado. Com o uso de HNO3 concentrado obteve-se uma concentração de C residual de 123 mg L-1 e uma elevada acidez residual (7,7 mol L-1 de HNO3). Além disso, foi realizada a avaliação da eficiência de decomposição dos componentes da formulação das SNE, separadamente. Para isso, caseinato de sódio, xarope de glicose e óleo de girassol e canola foram decompostos com 8 mL de H2O2 50% v/v. Observou-se que o caseinato de sódio e os óleos de girassol e canola apresentaram os maiores concentrações de carbono residual. Além disso, foi realizada a decomposição de compostos orgânicos refratários à oxidação por via úmida tais como, histidina, triptofano, fenilalanina e ácido linoleico, utilizando o sistema SRC, H2O2 50% e HNO3 concentrado. Os valores de concentração de carbono residual (RCC), para estas substâncias orgânicas refratárias, foram significativamente menores do que reportados na literatura, provavelmente devido às condições de pressão e temperatura mais drásticas permitidas pelo sistema SRC. Por fim, foi feita a determinação de As, Ca, Cd, Co, Cr, Cu, Fe, K, Mg, Mn, Mo, Na, P, Pb, Se e Zn por ICP OES e ICP-MS e não foram observadas diferenças significativas entre os resultados obtidos pelos diferentes métodos. A exatidão também foi avaliada mediante análise de um material de referência (NIST 8435 Whole Milk Powder).Conselho Nacional de Pesquisa e Desenvolvimento Científico e Tecnológico - CNPqporUniversidade 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/openAccessSolução de nutrição enteralPreparo de amostraCâmara única de reaçãoH2O2Enteral nutrition solutionSample preparationSingle reaction chamberCNPQ::CIENCIAS EXATAS E DA TERRA::QUIMICADesenvolvimento de método de preparo de amostras de solução de nutrição enteral mediante sistema de digestão de alta pressão para posterior determinação multielementarDevelopment of sample preparation methods using high pressure digestion system for subsequent multielement determination in enteral nutrition solutioninfo:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/masterThesisMuller, Edson Irineuhttp://lattes.cnpq.br/5994311290376153Pozebon, Dircehttp://lattes.cnpq.br/1962782589609789Duarte, Fábio Andreihttp://lattes.cnpq.br/3503633944419329http://lattes.cnpq.br/9982376508192805Anschau, Kéllen Francine1006000000006007f625a4e-a794-459f-919f-05a72717620d2e97c036-ae76-4151-969c-ff105e80e7b8a10aee69-497f-4257-96b7-c8a42f2d96837b2cc41c-5584-4228-a9bf-b1eb4d91e1e4reponame:Biblioteca Digital de Teses e Dissertações do UFSMinstname:Universidade Federal de Santa Maria (UFSM)instacron:UFSMORIGINALDIS_PPGQUIMICA_2018_ANSCHAU_KELLEN.pdfDIS_PPGQUIMICA_2018_ANSCHAU_KELLEN.pdfDissertação de Mestradoapplication/pdf1637449http://repositorio.ufsm.br/bitstream/1/18684/1/DIS_PPGQUIMICA_2018_ANSCHAU_KELLEN.pdf9720edd0b6fa8693d5d957ebe4961058MD51LICENSElicense.txtlicense.txttext/plain; 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dc.title.por.fl_str_mv Desenvolvimento de método de preparo de amostras de solução de nutrição enteral mediante sistema de digestão de alta pressão para posterior determinação multielementar
dc.title.alternative.eng.fl_str_mv Development of sample preparation methods using high pressure digestion system for subsequent multielement determination in enteral nutrition solution
title Desenvolvimento de método de preparo de amostras de solução de nutrição enteral mediante sistema de digestão de alta pressão para posterior determinação multielementar
spellingShingle Desenvolvimento de método de preparo de amostras de solução de nutrição enteral mediante sistema de digestão de alta pressão para posterior determinação multielementar
Anschau, Kéllen Francine
Solução de nutrição enteral
Preparo de amostra
Câmara única de reação
H2O2
Enteral nutrition solution
Sample preparation
Single reaction chamber
CNPQ::CIENCIAS EXATAS E DA TERRA::QUIMICA
title_short Desenvolvimento de método de preparo de amostras de solução de nutrição enteral mediante sistema de digestão de alta pressão para posterior determinação multielementar
title_full Desenvolvimento de método de preparo de amostras de solução de nutrição enteral mediante sistema de digestão de alta pressão para posterior determinação multielementar
title_fullStr Desenvolvimento de método de preparo de amostras de solução de nutrição enteral mediante sistema de digestão de alta pressão para posterior determinação multielementar
title_full_unstemmed Desenvolvimento de método de preparo de amostras de solução de nutrição enteral mediante sistema de digestão de alta pressão para posterior determinação multielementar
title_sort Desenvolvimento de método de preparo de amostras de solução de nutrição enteral mediante sistema de digestão de alta pressão para posterior determinação multielementar
author Anschau, Kéllen Francine
author_facet Anschau, Kéllen Francine
author_role author
dc.contributor.advisor1.fl_str_mv Muller, Edson Irineu
dc.contributor.advisor1Lattes.fl_str_mv http://lattes.cnpq.br/5994311290376153
dc.contributor.referee1.fl_str_mv Pozebon, Dirce
dc.contributor.referee1Lattes.fl_str_mv http://lattes.cnpq.br/1962782589609789
dc.contributor.referee2.fl_str_mv Duarte, Fábio Andrei
dc.contributor.referee2Lattes.fl_str_mv http://lattes.cnpq.br/3503633944419329
dc.contributor.authorLattes.fl_str_mv http://lattes.cnpq.br/9982376508192805
dc.contributor.author.fl_str_mv Anschau, Kéllen Francine
contributor_str_mv Muller, Edson Irineu
Pozebon, Dirce
Duarte, Fábio Andrei
dc.subject.por.fl_str_mv Solução de nutrição enteral
Preparo de amostra
Câmara única de reação
H2O2
topic Solução de nutrição enteral
Preparo de amostra
Câmara única de reação
H2O2
Enteral nutrition solution
Sample preparation
Single reaction chamber
CNPQ::CIENCIAS EXATAS E DA TERRA::QUIMICA
dc.subject.eng.fl_str_mv Enteral nutrition solution
Sample preparation
Single reaction chamber
dc.subject.cnpq.fl_str_mv CNPQ::CIENCIAS EXATAS E DA TERRA::QUIMICA
description In this work two methods of sample preparation for the digestion of enteral nutrition solution (SNE) using microwave assisted digestion (MWAD) in a single reaction chamber (SRC) system and subsequent multielement determination by plasma-based techniques (ICP OES and ICP-MS) were evaluated. For H2O2, parameters such as H2O2 concentration (30, 40 and 50%), temperature of the SRC system (190, 230 and 250 ° C), volume of H2O2 (6, 8 and 10 mL) and the sample mass (ranging from 250 mg to 1500 mg) were investigated. The evaluation of the best condition was made based on the concentration of residual C and the residual acidity of the digests. The best condition for the SRC system with H2O2 was 8 mL of 50% H2O2, temperature of 250 ° C and mass of 1000 mg of SNE. In this condition, the residual C concentration obtained was 711 mg L-1 and negligible residual acidity. Subsequently, the best condition obtained with H2O2 was also applied to concentrated HNO3. Using concentrated HNO3, a residual C concentration of 123 mg L-1 and a high residual acidity (7,7 mol L-1 of HNO3) were obtained. In addition, the decomposition efficiency of the components of the SNE formulation were evaluated. For this, sodium caseinate, glucose syrup and sunflower and canola oils were digested using 8 mL of 50% H2O2. It was observed that sodium caseinate and sunflower and canola oils had the highest values of residual carbon. In addition, wet digestion of refractory organic compounds such as histidine, tryptophan, phenylalanine and linoleic acid was performed using the SRC system with 50% H2O2 and concentrated HNO3. The values of residual carbon content (RCC) obtained for these refractory organic substances were significantly lower than reported in the literature, probably due to the more drastic pressure and temperature conditions allowed by the SRC system. Finally, the determination of As, Ca, Cd, Co, Cr, Cu, Fe, K, Mg, Mn, Mo, Na, P, Pb, Se and Zn were performed by ICP OES and ICP-MS and were not observed significant differences between the results obtained by the methods that used 50% H2O2 and concentrated HNO3. The accuracy was also evaluated with a reference material (NIST 8435 Whole Milk Powder).
publishDate 2018
dc.date.issued.fl_str_mv 2018-03-01
dc.date.accessioned.fl_str_mv 2019-10-25T18:27:58Z
dc.date.available.fl_str_mv 2019-10-25T18:27:58Z
dc.type.status.fl_str_mv info:eu-repo/semantics/publishedVersion
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dc.identifier.uri.fl_str_mv http://repositorio.ufsm.br/handle/1/18684
url http://repositorio.ufsm.br/handle/1/18684
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language por
dc.relation.cnpq.fl_str_mv 100600000000
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dc.rights.driver.fl_str_mv Attribution-NonCommercial-NoDerivatives 4.0 International
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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
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