Desenvolvimento de sistemas à base de mesocarpo de babaçu e alginato de sódio como matriz carregadora do fármaco metronidazol

Detalhes bibliográficos
Autor(a) principal: OLIVEIRA, Letícia Nascimento de
Data de Publicação: 2021
Tipo de documento: Dissertação
Idioma: por
Título da fonte: Biblioteca Digital de Teses e Dissertações da UFMA
Texto Completo: https://tedebc.ufma.br/jspui/handle/tede/tede/3727
Resumo: This work aimed to evaluate spheres based on sodium alginate and starch extracted from babassu mesocarp as a matrix for the controlled release of the drug metronidazole. The starch was obtained by water extraction method and the same was synthesized using chloroacetic acid as etherifying agent, resulting in carboxymethylamides with degrees of substitution (GS) of 0.15 ± 0.01 and 0.3 ± 0.01. The solubility and intumescence study of the starch and carboxymethylamide samples showed changes in the properties after modification. The study of amylose content of native and modified starch using colorimetric method showed a large variation in amylose content, from 28.0 ± 0.89, 4.70 ± 0.21 and 3.32 ± 0.04, proving the reduction of the macromolecule after modification. The starch and carboxymethyl starch samples were characterized by FTIR, SEM and DSC. The drug metronidazole was incorporated into sodium alginate/ babassu mesocarp starch and sodium alginate/carboxymethyl starch polymeric matrices, obtaining spheres through ionotropic gelation in a CaCl2 solution. The interaction between the polysaccharides and the incorporation of the drug were proven by FTIR and SEM results. Energy Dispersive Spectroscopy (EDS) analysis enabled the detection of elements such as Ca, Na, Cl and O, as well as the percentage changes that occurred after polymer mixing. A molecular absorption study in the ultraviolet region proved the presence of the drug metronidazole incorporated in the spheres. The study of intumescence and erosion of the spheres showed that the absorption capacity of the spheres was improved in the spheres containing the CMA, which also influenced the erosion that was decreased with the increase in the degree of substitution of the anionic starch. The encapsulation efficiency (EE) varied according to the composition of the spheres. For the alginate and alginate/raw starch spheres the EE was 36.0% ± 5.40 and 53% ± 4.23 and for the alginate/carboxymethyl starch spheres, the EE obtained was 69.57% ± 3.94 and 73.89% ± 5.22. The release assays demonstrated that in gastric medium, the spheres showed a low dissolution rate, suggesting gastroresistance at low pH. In simulated enteric medium, the ALG.CMA2 samples (GS = 0.3) maintained the same dissolution rate until the end of the experiment, suggesting a control in the release of metronidazole. Thus, it was possible to prove that the samples containing carboxymethyl starch are promising delivery systems for the sustained release of the drug under gastrointestinal conditions.
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spelling SANTANA, Sirlane Aparecida Abreuhttp://lattes.cnpq.br/1052349578152491SANTANA, Sirlane Aparecida Abreuhttp://lattes.cnpq.br/1052349578152491ALCÂNTARA, Ana Clécia Santos dehttp://lattes.cnpq.br/3149929057352643ROCHA, Jefferson Almeidahttp://lattes.cnpq.br/5340332707224756OLIVEIRA, Letícia Nascimento de2022-06-21T17:05:59Z2021-11-24OLIVEIRA, Letícia Nascimento de. . 2021. Desenvolvimento de sistemas à base de mesocarpo de babaçu e alginato de sódio como matriz carregadora do fármaco metronidazol.91 f. Dissertação (Programa de Pós-Graduação em Química/CCET) - Universidade Federal do Maranhão, São Luís, 2021https://tedebc.ufma.br/jspui/handle/tede/tede/3727This work aimed to evaluate spheres based on sodium alginate and starch extracted from babassu mesocarp as a matrix for the controlled release of the drug metronidazole. The starch was obtained by water extraction method and the same was synthesized using chloroacetic acid as etherifying agent, resulting in carboxymethylamides with degrees of substitution (GS) of 0.15 ± 0.01 and 0.3 ± 0.01. The solubility and intumescence study of the starch and carboxymethylamide samples showed changes in the properties after modification. The study of amylose content of native and modified starch using colorimetric method showed a large variation in amylose content, from 28.0 ± 0.89, 4.70 ± 0.21 and 3.32 ± 0.04, proving the reduction of the macromolecule after modification. The starch and carboxymethyl starch samples were characterized by FTIR, SEM and DSC. The drug metronidazole was incorporated into sodium alginate/ babassu mesocarp starch and sodium alginate/carboxymethyl starch polymeric matrices, obtaining spheres through ionotropic gelation in a CaCl2 solution. The interaction between the polysaccharides and the incorporation of the drug were proven by FTIR and SEM results. Energy Dispersive Spectroscopy (EDS) analysis enabled the detection of elements such as Ca, Na, Cl and O, as well as the percentage changes that occurred after polymer mixing. A molecular absorption study in the ultraviolet region proved the presence of the drug metronidazole incorporated in the spheres. The study of intumescence and erosion of the spheres showed that the absorption capacity of the spheres was improved in the spheres containing the CMA, which also influenced the erosion that was decreased with the increase in the degree of substitution of the anionic starch. The encapsulation efficiency (EE) varied according to the composition of the spheres. For the alginate and alginate/raw starch spheres the EE was 36.0% ± 5.40 and 53% ± 4.23 and for the alginate/carboxymethyl starch spheres, the EE obtained was 69.57% ± 3.94 and 73.89% ± 5.22. The release assays demonstrated that in gastric medium, the spheres showed a low dissolution rate, suggesting gastroresistance at low pH. In simulated enteric medium, the ALG.CMA2 samples (GS = 0.3) maintained the same dissolution rate until the end of the experiment, suggesting a control in the release of metronidazole. Thus, it was possible to prove that the samples containing carboxymethyl starch are promising delivery systems for the sustained release of the drug under gastrointestinal conditions.Este trabalho teve como objetivo avaliar esferas à base de alginato de sódio e amido extraído do mesocarpo do babaçu como uma matriz para a liberação controlada do fármaco metronidazol. O amido foi obtido pelo método de extração em água e o mesmo foi sintetizado o ácido cloroacético como agente eterificante, resultado em carboximetilamidos com graus de substituição (GS) de 0,15 ± 0,01 e 0,3 ± 0,01. O estudo de solubilidade e intumescimento das amostras do amido e carboximetilamido mostraram mudanças nas propriedades após a modificação. O estudo do teor amilose do amido nativo e modificado, utilizando método colorimétrico apresentou uma grande variação no teor de amilose, de 28,0 ± 0,89, 4,70 ± 0,21 e 3,32 ± 0,04, comprovando a redução da macromolécula após a modificação. As amostras de amido e carboximetilamido foram caracterizadas por FTIR, MEV e DSC. O fármaco metronidazol foi incorporado as matrizes poliméricas de alginato de sódio/amido do mesocarpo do babaçu e alginato de sódio/carboximetilamido, obtendo esferas através da gelificação ionotrópica em uma solução de CaCl2. A interação entre os polissacarídeos e a incorporação do fármaco foram comprovadas pelos resultados do FTIR e MEV. A análise por Espectroscopia de Energia Dispersiva (EDS) possibilitou a detecção de elementos como Ca, Na, Cl e O, bem como as alterações percentuais ocorridas após a mistura polimérica. Um estudo de absorção molecular na região do ultravioleta comprovou a presença do fármaco metronidazol incorporado nas esferas. O estudo de intumescimento e erosão das esferas mostrou que a capacidade de absorção das esferas foi melhorada nas esferas contendo o CMA, que também influenciou na erosão que foi diminuída com o aumento do grau de substituição do amido aniônico. A eficiência de encapsulamento (EE) variou de acordo com a a composição das esferas. Nas esferas de alginato e alginato/amido in natura a EE foi 36,0% ± 5,40 e 53% ± 4,23 e para as esferas de alginato/carboximetilamido, a EE obtida foi 69,57% ± 3,94 e 73,89% ± 5,22. Os ensaios de liberação demonstraram que em meio gástrico, as esferas apresentaram uma baixa taxa de dissolução, sugerindo uma gastrorresistência em pH baixo. Em meio entérico simulado, as amostras de ALG.CMA2 (GS = 0,3) manteve a mesma taxa de dissolução até o término do experimento, sugerindo um controle na liberação do metronidazol. Dessa forma foi possível comprovar que as amostras contendo carboximetilamido são sistemas de entregas promissores para a liberação sustentada da droga em condições gastrointestinais.Submitted by Daniella Santos (daniella.santos@ufma.br) on 2022-06-21T17:05:59Z No. of bitstreams: 1 LetíciaOliveira.pdf: 2168643 bytes, checksum: 8a8753efb4489bd055e10963078944bc (MD5)Made available in DSpace on 2022-06-21T17:05:59Z (GMT). No. of bitstreams: 1 LetíciaOliveira.pdf: 2168643 bytes, checksum: 8a8753efb4489bd055e10963078944bc (MD5) Previous issue date: 2021-11-24FAPEMAapplication/pdfporUniversidade Federal do MaranhãoPROGRAMA DE PÓS-GRADUAÇÃO EM QUÍMICA/CCETUFMABrasilDEPARTAMENTO DE QUÍMICA/CCETmisturas poliméricas;mesocarpo do babaçu;carboximetilação do amido;liberação de fármaco;polymeric mixtures;babassu mesocarp;starch carboxymethylation;drug release.QuímicaDesenvolvimento de sistemas à base de mesocarpo de babaçu e alginato de sódio como matriz carregadora do fármaco metronidazolDevelopment of systems based on babassu mesocarp and sodium alginate as a carrier matrix for the drug metronidazoleinfo:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/masterThesisinfo:eu-repo/semantics/openAccessreponame:Biblioteca Digital de Teses e Dissertações da UFMAinstname:Universidade Federal do Maranhão (UFMA)instacron:UFMAORIGINALLetíciaOliveira.pdfLetíciaOliveira.pdfapplication/pdf2168643http://tedebc.ufma.br:8080/bitstream/tede/3727/2/Let%C3%ADciaOliveira.pdf8a8753efb4489bd055e10963078944bcMD52LICENSElicense.txtlicense.txttext/plain; charset=utf-82255http://tedebc.ufma.br:8080/bitstream/tede/3727/1/license.txt97eeade1fce43278e63fe063657f8083MD51tede/37272022-07-04 08:27:43.674oai:tede2: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Biblioteca Digital de Teses e Dissertaçõeshttps://tedebc.ufma.br/jspui/PUBhttp://tedebc.ufma.br:8080/oai/requestrepositorio@ufma.br||repositorio@ufma.bropendoar:21312022-07-04T11:27:43Biblioteca Digital de Teses e Dissertações da UFMA - Universidade Federal do Maranhão (UFMA)false
dc.title.por.fl_str_mv Desenvolvimento de sistemas à base de mesocarpo de babaçu e alginato de sódio como matriz carregadora do fármaco metronidazol
dc.title.alternative.eng.fl_str_mv Development of systems based on babassu mesocarp and sodium alginate as a carrier matrix for the drug metronidazole
title Desenvolvimento de sistemas à base de mesocarpo de babaçu e alginato de sódio como matriz carregadora do fármaco metronidazol
spellingShingle Desenvolvimento de sistemas à base de mesocarpo de babaçu e alginato de sódio como matriz carregadora do fármaco metronidazol
OLIVEIRA, Letícia Nascimento de
misturas poliméricas;
mesocarpo do babaçu;
carboximetilação do amido;
liberação de fármaco;
polymeric mixtures;
babassu mesocarp;
starch carboxymethylation;
drug release.
Química
title_short Desenvolvimento de sistemas à base de mesocarpo de babaçu e alginato de sódio como matriz carregadora do fármaco metronidazol
title_full Desenvolvimento de sistemas à base de mesocarpo de babaçu e alginato de sódio como matriz carregadora do fármaco metronidazol
title_fullStr Desenvolvimento de sistemas à base de mesocarpo de babaçu e alginato de sódio como matriz carregadora do fármaco metronidazol
title_full_unstemmed Desenvolvimento de sistemas à base de mesocarpo de babaçu e alginato de sódio como matriz carregadora do fármaco metronidazol
title_sort Desenvolvimento de sistemas à base de mesocarpo de babaçu e alginato de sódio como matriz carregadora do fármaco metronidazol
author OLIVEIRA, Letícia Nascimento de
author_facet OLIVEIRA, Letícia Nascimento de
author_role author
dc.contributor.advisor1.fl_str_mv SANTANA, Sirlane Aparecida Abreu
dc.contributor.advisor1Lattes.fl_str_mv http://lattes.cnpq.br/1052349578152491
dc.contributor.referee1.fl_str_mv SANTANA, Sirlane Aparecida Abreu
dc.contributor.referee1Lattes.fl_str_mv http://lattes.cnpq.br/1052349578152491
dc.contributor.referee2.fl_str_mv ALCÂNTARA, Ana Clécia Santos de
dc.contributor.referee2Lattes.fl_str_mv http://lattes.cnpq.br/3149929057352643
dc.contributor.referee3.fl_str_mv ROCHA, Jefferson Almeida
dc.contributor.authorLattes.fl_str_mv http://lattes.cnpq.br/5340332707224756
dc.contributor.author.fl_str_mv OLIVEIRA, Letícia Nascimento de
contributor_str_mv SANTANA, Sirlane Aparecida Abreu
SANTANA, Sirlane Aparecida Abreu
ALCÂNTARA, Ana Clécia Santos de
ROCHA, Jefferson Almeida
dc.subject.por.fl_str_mv misturas poliméricas;
mesocarpo do babaçu;
carboximetilação do amido;
liberação de fármaco;
topic misturas poliméricas;
mesocarpo do babaçu;
carboximetilação do amido;
liberação de fármaco;
polymeric mixtures;
babassu mesocarp;
starch carboxymethylation;
drug release.
Química
dc.subject.eng.fl_str_mv polymeric mixtures;
babassu mesocarp;
starch carboxymethylation;
drug release.
dc.subject.cnpq.fl_str_mv Química
description This work aimed to evaluate spheres based on sodium alginate and starch extracted from babassu mesocarp as a matrix for the controlled release of the drug metronidazole. The starch was obtained by water extraction method and the same was synthesized using chloroacetic acid as etherifying agent, resulting in carboxymethylamides with degrees of substitution (GS) of 0.15 ± 0.01 and 0.3 ± 0.01. The solubility and intumescence study of the starch and carboxymethylamide samples showed changes in the properties after modification. The study of amylose content of native and modified starch using colorimetric method showed a large variation in amylose content, from 28.0 ± 0.89, 4.70 ± 0.21 and 3.32 ± 0.04, proving the reduction of the macromolecule after modification. The starch and carboxymethyl starch samples were characterized by FTIR, SEM and DSC. The drug metronidazole was incorporated into sodium alginate/ babassu mesocarp starch and sodium alginate/carboxymethyl starch polymeric matrices, obtaining spheres through ionotropic gelation in a CaCl2 solution. The interaction between the polysaccharides and the incorporation of the drug were proven by FTIR and SEM results. Energy Dispersive Spectroscopy (EDS) analysis enabled the detection of elements such as Ca, Na, Cl and O, as well as the percentage changes that occurred after polymer mixing. A molecular absorption study in the ultraviolet region proved the presence of the drug metronidazole incorporated in the spheres. The study of intumescence and erosion of the spheres showed that the absorption capacity of the spheres was improved in the spheres containing the CMA, which also influenced the erosion that was decreased with the increase in the degree of substitution of the anionic starch. The encapsulation efficiency (EE) varied according to the composition of the spheres. For the alginate and alginate/raw starch spheres the EE was 36.0% ± 5.40 and 53% ± 4.23 and for the alginate/carboxymethyl starch spheres, the EE obtained was 69.57% ± 3.94 and 73.89% ± 5.22. The release assays demonstrated that in gastric medium, the spheres showed a low dissolution rate, suggesting gastroresistance at low pH. In simulated enteric medium, the ALG.CMA2 samples (GS = 0.3) maintained the same dissolution rate until the end of the experiment, suggesting a control in the release of metronidazole. Thus, it was possible to prove that the samples containing carboxymethyl starch are promising delivery systems for the sustained release of the drug under gastrointestinal conditions.
publishDate 2021
dc.date.issued.fl_str_mv 2021-11-24
dc.date.accessioned.fl_str_mv 2022-06-21T17:05:59Z
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 OLIVEIRA, Letícia Nascimento de. . 2021. Desenvolvimento de sistemas à base de mesocarpo de babaçu e alginato de sódio como matriz carregadora do fármaco metronidazol.91 f. Dissertação (Programa de Pós-Graduação em Química/CCET) - Universidade Federal do Maranhão, São Luís, 2021
dc.identifier.uri.fl_str_mv https://tedebc.ufma.br/jspui/handle/tede/tede/3727
identifier_str_mv OLIVEIRA, Letícia Nascimento de. . 2021. Desenvolvimento de sistemas à base de mesocarpo de babaçu e alginato de sódio como matriz carregadora do fármaco metronidazol.91 f. Dissertação (Programa de Pós-Graduação em Química/CCET) - Universidade Federal do Maranhão, São Luís, 2021
url https://tedebc.ufma.br/jspui/handle/tede/tede/3727
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 application/pdf
dc.publisher.none.fl_str_mv Universidade Federal do Maranhão
dc.publisher.program.fl_str_mv PROGRAMA DE PÓS-GRADUAÇÃO EM QUÍMICA/CCET
dc.publisher.initials.fl_str_mv UFMA
dc.publisher.country.fl_str_mv Brasil
dc.publisher.department.fl_str_mv DEPARTAMENTO DE QUÍMICA/CCET
publisher.none.fl_str_mv Universidade Federal do Maranhão
dc.source.none.fl_str_mv reponame:Biblioteca Digital de Teses e Dissertações da UFMA
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institution UFMA
reponame_str Biblioteca Digital de Teses e Dissertações da UFMA
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