Determinação elementar e avaliação da geração química de vapor para determinação simultânea de As e Hg em suplementos alimentares por MIP OES

Detalhes bibliográficos
Autor(a) principal: Bitencourt, Gustavo Rossato
Data de Publicação: 2021
Tipo de documento: Dissertação
Idioma: por
Título da fonte: Manancial - Repositório Digital da UFSM
Texto Completo: http://repositorio.ufsm.br/handle/1/23942
Resumo: In this work the suitability of microwave induced plasma optical emission spectrometry (MIP OES) for the determination of essential and non-essential elements in dietary supplements was evaluated. In this purpose, thirteen dietary supplement samples of several classifications (vitamins/minerals, minerals, amino acids, and botanicals) were digested by microwave-assisted wet digestion (MAWD) in their whole form for further determination of essential (Ca, Co, Cu, Fe, K, Mg, Mn, Mo, Na, and Zn) and non-essential (Ag, Al, B, Ba, Be, Cd, Cr, La, Li, Ni, Pb, Sr, and V) elements by MIP OES. After defining the most suitable operating conditions for MIP OES, potential interferences by major concomitants (C, Cl, Ca, K, Na, and S) were evaluated, as well as those by residual acidity of digests. The feasibility of the simultaneous determination of As and Hg by CVG-MIP OES was also evaluated, looking to obtain limits of quantification (LOQs) in compliance with maximum concentrations allowed for these elements in dietary supplements according to USP General Chapter 2232 and EC 629/2008 (only for Hg). A multimode sample introduction system (MSIS) was used, and several system setups were evaluated to improve the signal-to-noise ratio. The critical conditions for volatile species generation were optimized, as the reagents concentrations (NaBH4 and HCl), the reaction coil length, the flow-rate, and methods for the pre-reduction of As5+ to As3+. After optimizing the determination conditions, the study of interferences showed a suppression in some situations leading to a minimum dilution factor (2 and 50-fold) to samples with higher concentrations of Ca, Na, and K. The LOQs were in the range of 0.010 (Be) to 39.2 μg g-1 (Ca) and were dependent on the sample mass used for decomposition (from 0.6 to 1.6 g in the commercial product). There was a prevalence of essential and non-essential elements in vitamins/minerals, minerals, and botanicals dietary supplements, whereas lower concentrations were found in the dietary supplements of amino acids. Although the concentration of many elements was not in agreement with that which is labeled, all were in a concentration below the recommended dietary allowances (RDAs), exception for those with the concentration intentionally higher. Accuracy of results obtained by MIP OES was evaluated by comparison with those obtained by ICP OES and/or ICP-MS, with no statistical difference between them (t-test). Moreover, for the CRMs NIST 1572 and NIST 1575a, the results showed no statistical difference with the certified values (t-test). For the simultaneous determination of As and Hg by CVG-MIP OES, a suitable condition was established that led to signal improvement by 3 and 12-fold for As and Hg, respectively, compared with those intensities obtained using conventional nebulization. The LOQs obtained for As and Hg ranged from 0.058 to 0.187 and 0.126 to 0.403 μg g-1, respectively, which were below 1.5 μg g-1, limit stipulated by USP normative for both elements. Whereas the concentration of Hg in all samples was below to the LOQs, the concentration of As ranged from 0.099 to 0.274 μg g-1. The results by CVG-MIP OES presented no statistical difference with those obtained by ICP-MS for As (after decomposition by combustion) and CVG-ICP-MS, for Hg (after MAWD) (t-test). For the CRMs NIST 1572 and NIST 1575a, the results by CVG-MIP OES for As and Hg showed no statistical difference when compared to the certified values (t-test). Also, recovery tests at three concentration levels were performed for As and Hg and recoveries ranged from 93 to 108%. The MIP OES proved to be a suitable technique for the determination of essential and non-essential elements, including As and Hg by CVG-MIP OES, in dietary supplements, demonstrating to be a feasible alternative to the quality control of these products.
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spelling Determinação elementar e avaliação da geração química de vapor para determinação simultânea de As e Hg em suplementos alimentares por MIP OESElemental determination and evaluation of chemical vapor generation for simultaneous determination of As and Hg in dietary supplements by MIP OESMIP OESSuplementos alimentaresElementos essenciaisElementos não essenciaisCVG-MIP OESDietary supplementsEssential elementsNon-essential elementsCNPQ::CIENCIAS EXATAS E DA TERRA::QUIMICAIn this work the suitability of microwave induced plasma optical emission spectrometry (MIP OES) for the determination of essential and non-essential elements in dietary supplements was evaluated. In this purpose, thirteen dietary supplement samples of several classifications (vitamins/minerals, minerals, amino acids, and botanicals) were digested by microwave-assisted wet digestion (MAWD) in their whole form for further determination of essential (Ca, Co, Cu, Fe, K, Mg, Mn, Mo, Na, and Zn) and non-essential (Ag, Al, B, Ba, Be, Cd, Cr, La, Li, Ni, Pb, Sr, and V) elements by MIP OES. After defining the most suitable operating conditions for MIP OES, potential interferences by major concomitants (C, Cl, Ca, K, Na, and S) were evaluated, as well as those by residual acidity of digests. The feasibility of the simultaneous determination of As and Hg by CVG-MIP OES was also evaluated, looking to obtain limits of quantification (LOQs) in compliance with maximum concentrations allowed for these elements in dietary supplements according to USP General Chapter 2232 and EC 629/2008 (only for Hg). A multimode sample introduction system (MSIS) was used, and several system setups were evaluated to improve the signal-to-noise ratio. The critical conditions for volatile species generation were optimized, as the reagents concentrations (NaBH4 and HCl), the reaction coil length, the flow-rate, and methods for the pre-reduction of As5+ to As3+. After optimizing the determination conditions, the study of interferences showed a suppression in some situations leading to a minimum dilution factor (2 and 50-fold) to samples with higher concentrations of Ca, Na, and K. The LOQs were in the range of 0.010 (Be) to 39.2 μg g-1 (Ca) and were dependent on the sample mass used for decomposition (from 0.6 to 1.6 g in the commercial product). There was a prevalence of essential and non-essential elements in vitamins/minerals, minerals, and botanicals dietary supplements, whereas lower concentrations were found in the dietary supplements of amino acids. Although the concentration of many elements was not in agreement with that which is labeled, all were in a concentration below the recommended dietary allowances (RDAs), exception for those with the concentration intentionally higher. Accuracy of results obtained by MIP OES was evaluated by comparison with those obtained by ICP OES and/or ICP-MS, with no statistical difference between them (t-test). Moreover, for the CRMs NIST 1572 and NIST 1575a, the results showed no statistical difference with the certified values (t-test). For the simultaneous determination of As and Hg by CVG-MIP OES, a suitable condition was established that led to signal improvement by 3 and 12-fold for As and Hg, respectively, compared with those intensities obtained using conventional nebulization. The LOQs obtained for As and Hg ranged from 0.058 to 0.187 and 0.126 to 0.403 μg g-1, respectively, which were below 1.5 μg g-1, limit stipulated by USP normative for both elements. Whereas the concentration of Hg in all samples was below to the LOQs, the concentration of As ranged from 0.099 to 0.274 μg g-1. The results by CVG-MIP OES presented no statistical difference with those obtained by ICP-MS for As (after decomposition by combustion) and CVG-ICP-MS, for Hg (after MAWD) (t-test). For the CRMs NIST 1572 and NIST 1575a, the results by CVG-MIP OES for As and Hg showed no statistical difference when compared to the certified values (t-test). Also, recovery tests at three concentration levels were performed for As and Hg and recoveries ranged from 93 to 108%. The MIP OES proved to be a suitable technique for the determination of essential and non-essential elements, including As and Hg by CVG-MIP OES, in dietary supplements, demonstrating to be a feasible alternative to the quality control of these products.Coordenação de Aperfeiçoamento de Pessoal de Nível Superior - CAPESNeste trabalho foi avaliada a adequabilidade da técnica de espectrometria de emissão óptica com plasma induzido por micro-ondas (MIP OES) para a determinação de elementos essenciais e não essenciais em suplementos alimentares. Para isso, treze amostras de suplementos alimentares de diferentes composições (vitamínicos/minerais, minerais, aminoácidos e botânicos) foram decompostas na sua forma original utilizando o método de decomposição por via úmida assistida por radiação micro-ondas (MAWD) para posterior determinação de elementos essenciais (Ca, Co, Cu, Fe, K, Mg, Mn, Mo, Na e Zn) e não essenciais (Ag, Al, B, Ba, Be, Cd, Cr, La, Li, Ni, Pb, Sr e V) por MIP OES. Após a definição das condições operacionais mais adequadas para a determinação por MIP OES, foram avaliadas potenciais interferências provocadas por concomitantes majoritários (C, Cl, Ca, K, Na e S), bem como pela acidez residual dos digeridos. A viabilidade da determinação simultânea de As e Hg por CVG-MIP OES também foi avaliada, buscando a obtenção de limites de quantificação (LQs) que atendessem às concentrações máximas permitidas para esses elementos em suplementos alimentares, segundo as normas USP General Chapter 2232 e EC 629/2008 (apenas para Hg). Foi utilizada uma câmara de nebulização multimodo (MSIS), sendo avaliadas diferentes montagens do sistema para melhorar a razão sinal/ruído. Foram otimizadas as condições críticas de geração das espécies voláteis, como a concentração dos reagentes (NaBH4 e HCl), o comprimento do caminho reacional, a vazão das soluções e métodos de pré-redução do As5+ para As3+. Otimizadas as condições de determinação, a avaliação de interferências por concomitantes majoritários indicou supressão em algumas situações, o que levou a diluição dos digeridos (entre 2 e 50 vezes) para amostras com maiores concentrações de Ca, Na e K. Os LQs foram da ordem de 0,010 (Be) a 39,2 μg g-1 (Ca) e foram dependentes da massa de amostra utilizada para decomposição (de 0,6 a 1,6 g na formulação comercial). Observou-se prevalência de elementos essenciais e não essenciais nos suplementos alimentares vitamínicos/minerais, minerais e botânicos, enquanto que foram encontradas menores concentrações nos suplementos alimentares de aminoácidos. Apesar de a concentração encontrada para muitos elementos não estar de acordo com a informada nos rótulos, todos estavam presentes em concentração abaixo dos limites de exposição diários recomendados (RDAs), com exceção daqueles que possuem concentração acima, de forma intencional. A exatidão dos resultados obtidos pela técnica de MIP OES foi avaliada via comparação com os resultados por ICP OES e/ou ICP-MS, não tendo sido observada diferença estatística significativa entre eles (t-student). Além disso, para os CRMs NIST 1572 e 1575a os resultados não apresentaram diferença estatística significativa em relação aos valores certificados (t-student). Para a determinação simultânea de As e Hg por CVG-MIP OES foi estabelecida uma condição adequada que levou à melhora de 3 e 12 vezes nos sinais de As e Hg, respectivamente, quando comparados às intensidades obtidas utilizando a nebulização convencional. Os LQs obtidos para As e Hg por CVG-MIP OES foram de 0,058 a 0,187 e 0,126 a 0,403 μg g-1, respectivamente, os quais ficaram abaixo de 1,5 μg g-1, limite estipulado pela norma USP para ambos os elementos. Enquanto a concentração de Hg em todas as amostras ficou abaixo dos LQs do método, a concentração de As variou de 0,099 a 0,274 μg g-1. Os resultados por CVG-MIP OES não tiveram diferença estatística significativa em relação aos obtidos por ICP-MS para As (após decomposição por combustão) e CVG-ICP-MS, para Hg (após MAWD) (t-student). Para os CRMs NIST 1572 e 1575a os resultados por CVG-MIP OES para As e Hg não apresentaram diferença estatística significativa quando comparados com os valores certificados (t-student). Também, ensaios de recuperação em três níveis de concentração foram realizados para As e Hg, com recuperações variando de 93 a 108%. A técnica de MIP OES demonstrou-se ser adequada para a determinação de elementos essenciais e não essenciais, incluindo As e Hg por CVG-MIP OES, em suplementos alimentares, indicando ser uma opção viável para o controle de qualidade desses produtos.Universidade Federal de Santa MariaBrasilQuímicaUFSMPrograma de Pós-Graduação em QuímicaCentro de Ciências Naturais e ExatasMello, Paola de Azevedohttp://lattes.cnpq.br/2189500441942469Dressler, Valderi LuizSchiavo, DanielaBitencourt, Gustavo Rossato2022-03-25T17:26:22Z2022-03-25T17:26:22Z2021-09-09info:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/masterThesisapplication/pdfhttp://repositorio.ufsm.br/handle/1/23942porAttribution-NonCommercial-NoDerivatives 4.0 Internationalhttp://creativecommons.org/licenses/by-nc-nd/4.0/info:eu-repo/semantics/openAccessreponame:Manancial - Repositório Digital da UFSMinstname:Universidade Federal de Santa Maria (UFSM)instacron:UFSM2022-03-25T17:26:22Zoai:repositorio.ufsm.br:1/23942Biblioteca Digital de Teses e Dissertaçõeshttps://repositorio.ufsm.br/ONGhttps://repositorio.ufsm.br/oai/requestatendimento.sib@ufsm.br||tedebc@gmail.comopendoar:2022-03-25T17:26:22Manancial - Repositório Digital da UFSM - Universidade Federal de Santa Maria (UFSM)false
dc.title.none.fl_str_mv Determinação elementar e avaliação da geração química de vapor para determinação simultânea de As e Hg em suplementos alimentares por MIP OES
Elemental determination and evaluation of chemical vapor generation for simultaneous determination of As and Hg in dietary supplements by MIP OES
title Determinação elementar e avaliação da geração química de vapor para determinação simultânea de As e Hg em suplementos alimentares por MIP OES
spellingShingle Determinação elementar e avaliação da geração química de vapor para determinação simultânea de As e Hg em suplementos alimentares por MIP OES
Bitencourt, Gustavo Rossato
MIP OES
Suplementos alimentares
Elementos essenciais
Elementos não essenciais
CVG-MIP OES
Dietary supplements
Essential elements
Non-essential elements
CNPQ::CIENCIAS EXATAS E DA TERRA::QUIMICA
title_short Determinação elementar e avaliação da geração química de vapor para determinação simultânea de As e Hg em suplementos alimentares por MIP OES
title_full Determinação elementar e avaliação da geração química de vapor para determinação simultânea de As e Hg em suplementos alimentares por MIP OES
title_fullStr Determinação elementar e avaliação da geração química de vapor para determinação simultânea de As e Hg em suplementos alimentares por MIP OES
title_full_unstemmed Determinação elementar e avaliação da geração química de vapor para determinação simultânea de As e Hg em suplementos alimentares por MIP OES
title_sort Determinação elementar e avaliação da geração química de vapor para determinação simultânea de As e Hg em suplementos alimentares por MIP OES
author Bitencourt, Gustavo Rossato
author_facet Bitencourt, Gustavo Rossato
author_role author
dc.contributor.none.fl_str_mv Mello, Paola de Azevedo
http://lattes.cnpq.br/2189500441942469
Dressler, Valderi Luiz
Schiavo, Daniela
dc.contributor.author.fl_str_mv Bitencourt, Gustavo Rossato
dc.subject.por.fl_str_mv MIP OES
Suplementos alimentares
Elementos essenciais
Elementos não essenciais
CVG-MIP OES
Dietary supplements
Essential elements
Non-essential elements
CNPQ::CIENCIAS EXATAS E DA TERRA::QUIMICA
topic MIP OES
Suplementos alimentares
Elementos essenciais
Elementos não essenciais
CVG-MIP OES
Dietary supplements
Essential elements
Non-essential elements
CNPQ::CIENCIAS EXATAS E DA TERRA::QUIMICA
description In this work the suitability of microwave induced plasma optical emission spectrometry (MIP OES) for the determination of essential and non-essential elements in dietary supplements was evaluated. In this purpose, thirteen dietary supplement samples of several classifications (vitamins/minerals, minerals, amino acids, and botanicals) were digested by microwave-assisted wet digestion (MAWD) in their whole form for further determination of essential (Ca, Co, Cu, Fe, K, Mg, Mn, Mo, Na, and Zn) and non-essential (Ag, Al, B, Ba, Be, Cd, Cr, La, Li, Ni, Pb, Sr, and V) elements by MIP OES. After defining the most suitable operating conditions for MIP OES, potential interferences by major concomitants (C, Cl, Ca, K, Na, and S) were evaluated, as well as those by residual acidity of digests. The feasibility of the simultaneous determination of As and Hg by CVG-MIP OES was also evaluated, looking to obtain limits of quantification (LOQs) in compliance with maximum concentrations allowed for these elements in dietary supplements according to USP General Chapter 2232 and EC 629/2008 (only for Hg). A multimode sample introduction system (MSIS) was used, and several system setups were evaluated to improve the signal-to-noise ratio. The critical conditions for volatile species generation were optimized, as the reagents concentrations (NaBH4 and HCl), the reaction coil length, the flow-rate, and methods for the pre-reduction of As5+ to As3+. After optimizing the determination conditions, the study of interferences showed a suppression in some situations leading to a minimum dilution factor (2 and 50-fold) to samples with higher concentrations of Ca, Na, and K. The LOQs were in the range of 0.010 (Be) to 39.2 μg g-1 (Ca) and were dependent on the sample mass used for decomposition (from 0.6 to 1.6 g in the commercial product). There was a prevalence of essential and non-essential elements in vitamins/minerals, minerals, and botanicals dietary supplements, whereas lower concentrations were found in the dietary supplements of amino acids. Although the concentration of many elements was not in agreement with that which is labeled, all were in a concentration below the recommended dietary allowances (RDAs), exception for those with the concentration intentionally higher. Accuracy of results obtained by MIP OES was evaluated by comparison with those obtained by ICP OES and/or ICP-MS, with no statistical difference between them (t-test). Moreover, for the CRMs NIST 1572 and NIST 1575a, the results showed no statistical difference with the certified values (t-test). For the simultaneous determination of As and Hg by CVG-MIP OES, a suitable condition was established that led to signal improvement by 3 and 12-fold for As and Hg, respectively, compared with those intensities obtained using conventional nebulization. The LOQs obtained for As and Hg ranged from 0.058 to 0.187 and 0.126 to 0.403 μg g-1, respectively, which were below 1.5 μg g-1, limit stipulated by USP normative for both elements. Whereas the concentration of Hg in all samples was below to the LOQs, the concentration of As ranged from 0.099 to 0.274 μg g-1. The results by CVG-MIP OES presented no statistical difference with those obtained by ICP-MS for As (after decomposition by combustion) and CVG-ICP-MS, for Hg (after MAWD) (t-test). For the CRMs NIST 1572 and NIST 1575a, the results by CVG-MIP OES for As and Hg showed no statistical difference when compared to the certified values (t-test). Also, recovery tests at three concentration levels were performed for As and Hg and recoveries ranged from 93 to 108%. The MIP OES proved to be a suitable technique for the determination of essential and non-essential elements, including As and Hg by CVG-MIP OES, in dietary supplements, demonstrating to be a feasible alternative to the quality control of these products.
publishDate 2021
dc.date.none.fl_str_mv 2021-09-09
2022-03-25T17:26:22Z
2022-03-25T17:26:22Z
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.ufsm.br/handle/1/23942
url http://repositorio.ufsm.br/handle/1/23942
dc.language.iso.fl_str_mv por
language por
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.format.none.fl_str_mv application/pdf
dc.publisher.none.fl_str_mv Universidade Federal de Santa Maria
Brasil
Química
UFSM
Programa de Pós-Graduação em Química
Centro de Ciências Naturais e Exatas
publisher.none.fl_str_mv Universidade Federal de Santa Maria
Brasil
Química
UFSM
Programa de Pós-Graduação em Química
Centro de Ciências Naturais e Exatas
dc.source.none.fl_str_mv reponame:Manancial - Repositório Digital da 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 Manancial - Repositório Digital da UFSM
collection Manancial - Repositório Digital da UFSM
repository.name.fl_str_mv Manancial - Repositório Digital da UFSM - Universidade Federal de Santa Maria (UFSM)
repository.mail.fl_str_mv atendimento.sib@ufsm.br||tedebc@gmail.com
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