Avaliação do polissacarídeo da goma do cajueiro (Annacardium occidentale L.) como agente mucoadesivo e controlador da liberação em comprimidos matriciais
Autor(a) principal: | |
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Data de Publicação: | 2016 |
Tipo de documento: | Dissertação |
Idioma: | por |
Título da fonte: | Repositório Institucional da UFG |
dARK ID: | ark:/38995/00130000050kb |
Texto Completo: | http://repositorio.bc.ufg.br/tede/handle/tede/6766 |
Resumo: | Matricial tablets containing cashew gum polysaccharide (PGC) have been developed in order to promote mucoadhesion and prolonged release of model drugs with different water solubilities (theophylline and ketoprofen). Tablets were prepared by mixing the drug (40% m/m), diluent and PGC (10 to 50%, m/m). The control formulations were prepared by adding diluent instead polysaccharide. Tablets were prepared in a hydraulic press with 12.5 kN compaction force and 10s dwell time. Then, tablets were evaluated for their mechanical properties, drug content, drug in vitro release and mucoadhesive properties. The friability of the tablets met the limits recommended by the Brazilian Pharmacopoeia. The addition of the polysaccharide in the formulation significantly reduced the tablet hardness, which was also affected by the type of drug incorporated. The in vitro release test was carried out in acid medium (2h), followed by 0.4 M phosphate buffer pH 6.8 (6h). A more prolonged profile was achieved in ketoprofen-loaded tablets. In the case of theophylline-loaded tablets, prolonged release was less effective, even when the highest PGC concentration was used (50%, w/w). Ketoprofen-loaded tablets prepared with 30% of PGC released only 9% of the drug in acidic medium. In phosphate buffer, PGC tablets were capable to prolong ketoprofen release. Linearization of the drug release data showed that PGC tablets best fitted the Higuchi model. Mucoadhesion tests showed that the presence of polyssacharide increase tablet adhesion on the bowel membrane. The degree of mucoadhesion was dependent of the PGC concentration, it was greater when 30% (w/w) polysaccharide was added. The results suggests the use of cashew gum polysaccharide in matrix tablets for prolonged release of water-insoluble drugs and as mucoadhesive agent. |
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Marreto, Ricardo Neveshttp://lattes.cnpq.br/6127043775208484Marreto, Ricardo NevesFernandes, Kátia FláviaSouza, Leonardo Gomeshttp://lattes.cnpq.br/4668528219876286Oliveira, Aline Carlos de2017-01-19T10:30:52Z2016-09-22Oliveira, A. C. Avaliação do polissacarídeo da goma do cajueiro (Annacardium occidentale L.) como agente mucoadesivo e controlador da liberação em comprimidos matriciais. 2016. 54 f. Dissertação (Mestrado em Ciências Farmacêuticas) - Universidade Federal de Goiás, Goiânia, 2016.http://repositorio.bc.ufg.br/tede/handle/tede/6766ark:/38995/00130000050kbMatricial tablets containing cashew gum polysaccharide (PGC) have been developed in order to promote mucoadhesion and prolonged release of model drugs with different water solubilities (theophylline and ketoprofen). Tablets were prepared by mixing the drug (40% m/m), diluent and PGC (10 to 50%, m/m). The control formulations were prepared by adding diluent instead polysaccharide. Tablets were prepared in a hydraulic press with 12.5 kN compaction force and 10s dwell time. Then, tablets were evaluated for their mechanical properties, drug content, drug in vitro release and mucoadhesive properties. The friability of the tablets met the limits recommended by the Brazilian Pharmacopoeia. The addition of the polysaccharide in the formulation significantly reduced the tablet hardness, which was also affected by the type of drug incorporated. The in vitro release test was carried out in acid medium (2h), followed by 0.4 M phosphate buffer pH 6.8 (6h). A more prolonged profile was achieved in ketoprofen-loaded tablets. In the case of theophylline-loaded tablets, prolonged release was less effective, even when the highest PGC concentration was used (50%, w/w). Ketoprofen-loaded tablets prepared with 30% of PGC released only 9% of the drug in acidic medium. In phosphate buffer, PGC tablets were capable to prolong ketoprofen release. Linearization of the drug release data showed that PGC tablets best fitted the Higuchi model. Mucoadhesion tests showed that the presence of polyssacharide increase tablet adhesion on the bowel membrane. The degree of mucoadhesion was dependent of the PGC concentration, it was greater when 30% (w/w) polysaccharide was added. The results suggests the use of cashew gum polysaccharide in matrix tablets for prolonged release of water-insoluble drugs and as mucoadhesive agent.Comprimidos matriciais contendo polissacarídeo extraído da goma do cajueiro (PGC) foram desenvolvidos no intuito de promover mucoadesão e liberação prolongada de fármacos modelo com diferente solubilidade aquosa (teofilina e cetoprofeno). Os comprimidos foram preparados pela mistura de fármaco (40%, m/m), diluente e PGC, este último em concentração na faixa de 10 a 50% (m/m). Comprimidos controle, sem PGC, foram preparados pela substituição do polissacarídeo por diluente. A compactação foi realizada em prensa hidráulica com força de compressão de 12,5 KN exercida por 10 segundos. Os comprimidos foram avaliados quanto as suas propriedades mecânicas, teor e liberação in vitro dos fármacos incorporados e quanto à sua capacidade de mucoadesão ex vivo. A friabilidade dos comprimidos atendeu aos limites da Farmacopeia Brasileira. A adição do polissacarídeo na formulação diminuiu significativamente a dureza dos compactos, a qual também foi afetada pelo tipo de fármaco incorporado. O teste de liberação in vitro foi realizado em meio ácido (2h), seguido de tampão fosfato 0,4 M pH 6,8 (6h) e o maior prolongamento da liberação foi observado no caso do cetoprofeno. Não foi possível observar um prolongamento significativo na liberação da teofilina, mesmo com o aumento da concentração do polissacarídeo na formulação. Para o cetoprofeno, comprimidos contendo 30% de PGC, foram capazes de promover a liberação de apenas 9% do fármaco em meio ácido. Em pH 6,8 a liberação do cetoprofeno foi gradual. A linearização dos dados de liberação mostrou que o modelo de Higuchi foi o que melhor descreveu o comportamento das matrizes. Os testes de mucoadesão demonstraram que a presença do polissacarídeo conferiu mucoadesividade à forma farmacêutica. O grau de mucoadesão foi dependente da concentração do PGC na formulação, sendo maior quando 30% (m/m) do polissacarídeo foram adicionados à formulação. Os resultados sugerem o uso do PGC como agente prolongador da liberação de fármacos pouco solúveis em água em comprimidos matriciais, assim como demonstram seu potencial como agente mucoadesivo.Submitted by Erika Demachki (erikademachki@gmail.com) on 2017-01-18T16:16:10Z No. of bitstreams: 2 Dissertação - Aline Carlos de Oliveira - 2016.pdf: 1109303 bytes, checksum: 21ef921b9600f5b6723928640fb5b53f (MD5) license_rdf: 0 bytes, checksum: d41d8cd98f00b204e9800998ecf8427e (MD5)Approved for entry into archive by Luciana Ferreira (lucgeral@gmail.com) on 2017-01-19T10:30:52Z (GMT) No. of bitstreams: 2 Dissertação - Aline Carlos de Oliveira - 2016.pdf: 1109303 bytes, checksum: 21ef921b9600f5b6723928640fb5b53f (MD5) license_rdf: 0 bytes, checksum: d41d8cd98f00b204e9800998ecf8427e (MD5)Made available in DSpace on 2017-01-19T10:30:52Z (GMT). No. of bitstreams: 2 Dissertação - Aline Carlos de Oliveira - 2016.pdf: 1109303 bytes, checksum: 21ef921b9600f5b6723928640fb5b53f (MD5) license_rdf: 0 bytes, checksum: d41d8cd98f00b204e9800998ecf8427e (MD5) Previous issue date: 2016-09-22application/pdfporUniversidade Federal de GoiásPrograma de Pós-graduação em Ciências Farmacêuticas (FF)UFGBrasilFaculdade Farmácia - FF (RG)http://creativecommons.org/licenses/by-nc-nd/4.0/info:eu-repo/semantics/openAccessComprimidos matriciaisMucoadesãoPolissacarídeoGoma do cajueiroMatrix tabletsMucoadhesionPolysaccharideCashew gumCIENCIAS DA SAUDE::FARMACIAAvaliação do polissacarídeo da goma do cajueiro (Annacardium occidentale L.) como agente mucoadesivo e controlador da liberação em comprimidos matriciaisEvaluation of the cashew gum polysaccarid (Anacardium occidentale L.) as a mucoadesive agent and controller of release in matrical tabletsinfo:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/masterThesis82493698819615241260060060060102811615242093756997636413449754996reponame:Repositório Institucional da UFGinstname:Universidade Federal de Goiás (UFG)instacron:UFGLICENSElicense.txtlicense.txttext/plain; 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dc.title.por.fl_str_mv |
Avaliação do polissacarídeo da goma do cajueiro (Annacardium occidentale L.) como agente mucoadesivo e controlador da liberação em comprimidos matriciais |
dc.title.alternative.eng.fl_str_mv |
Evaluation of the cashew gum polysaccarid (Anacardium occidentale L.) as a mucoadesive agent and controller of release in matrical tablets |
title |
Avaliação do polissacarídeo da goma do cajueiro (Annacardium occidentale L.) como agente mucoadesivo e controlador da liberação em comprimidos matriciais |
spellingShingle |
Avaliação do polissacarídeo da goma do cajueiro (Annacardium occidentale L.) como agente mucoadesivo e controlador da liberação em comprimidos matriciais Oliveira, Aline Carlos de Comprimidos matriciais Mucoadesão Polissacarídeo Goma do cajueiro Matrix tablets Mucoadhesion Polysaccharide Cashew gum CIENCIAS DA SAUDE::FARMACIA |
title_short |
Avaliação do polissacarídeo da goma do cajueiro (Annacardium occidentale L.) como agente mucoadesivo e controlador da liberação em comprimidos matriciais |
title_full |
Avaliação do polissacarídeo da goma do cajueiro (Annacardium occidentale L.) como agente mucoadesivo e controlador da liberação em comprimidos matriciais |
title_fullStr |
Avaliação do polissacarídeo da goma do cajueiro (Annacardium occidentale L.) como agente mucoadesivo e controlador da liberação em comprimidos matriciais |
title_full_unstemmed |
Avaliação do polissacarídeo da goma do cajueiro (Annacardium occidentale L.) como agente mucoadesivo e controlador da liberação em comprimidos matriciais |
title_sort |
Avaliação do polissacarídeo da goma do cajueiro (Annacardium occidentale L.) como agente mucoadesivo e controlador da liberação em comprimidos matriciais |
author |
Oliveira, Aline Carlos de |
author_facet |
Oliveira, Aline Carlos de |
author_role |
author |
dc.contributor.advisor1.fl_str_mv |
Marreto, Ricardo Neves |
dc.contributor.advisor1Lattes.fl_str_mv |
http://lattes.cnpq.br/6127043775208484 |
dc.contributor.referee1.fl_str_mv |
Marreto, Ricardo Neves |
dc.contributor.referee2.fl_str_mv |
Fernandes, Kátia Flávia |
dc.contributor.referee3.fl_str_mv |
Souza, Leonardo Gomes |
dc.contributor.authorLattes.fl_str_mv |
http://lattes.cnpq.br/4668528219876286 |
dc.contributor.author.fl_str_mv |
Oliveira, Aline Carlos de |
contributor_str_mv |
Marreto, Ricardo Neves Marreto, Ricardo Neves Fernandes, Kátia Flávia Souza, Leonardo Gomes |
dc.subject.por.fl_str_mv |
Comprimidos matriciais Mucoadesão Polissacarídeo Goma do cajueiro |
topic |
Comprimidos matriciais Mucoadesão Polissacarídeo Goma do cajueiro Matrix tablets Mucoadhesion Polysaccharide Cashew gum CIENCIAS DA SAUDE::FARMACIA |
dc.subject.eng.fl_str_mv |
Matrix tablets Mucoadhesion Polysaccharide Cashew gum |
dc.subject.cnpq.fl_str_mv |
CIENCIAS DA SAUDE::FARMACIA |
description |
Matricial tablets containing cashew gum polysaccharide (PGC) have been developed in order to promote mucoadhesion and prolonged release of model drugs with different water solubilities (theophylline and ketoprofen). Tablets were prepared by mixing the drug (40% m/m), diluent and PGC (10 to 50%, m/m). The control formulations were prepared by adding diluent instead polysaccharide. Tablets were prepared in a hydraulic press with 12.5 kN compaction force and 10s dwell time. Then, tablets were evaluated for their mechanical properties, drug content, drug in vitro release and mucoadhesive properties. The friability of the tablets met the limits recommended by the Brazilian Pharmacopoeia. The addition of the polysaccharide in the formulation significantly reduced the tablet hardness, which was also affected by the type of drug incorporated. The in vitro release test was carried out in acid medium (2h), followed by 0.4 M phosphate buffer pH 6.8 (6h). A more prolonged profile was achieved in ketoprofen-loaded tablets. In the case of theophylline-loaded tablets, prolonged release was less effective, even when the highest PGC concentration was used (50%, w/w). Ketoprofen-loaded tablets prepared with 30% of PGC released only 9% of the drug in acidic medium. In phosphate buffer, PGC tablets were capable to prolong ketoprofen release. Linearization of the drug release data showed that PGC tablets best fitted the Higuchi model. Mucoadhesion tests showed that the presence of polyssacharide increase tablet adhesion on the bowel membrane. The degree of mucoadhesion was dependent of the PGC concentration, it was greater when 30% (w/w) polysaccharide was added. The results suggests the use of cashew gum polysaccharide in matrix tablets for prolonged release of water-insoluble drugs and as mucoadhesive agent. |
publishDate |
2016 |
dc.date.issued.fl_str_mv |
2016-09-22 |
dc.date.accessioned.fl_str_mv |
2017-01-19T10:30:52Z |
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, A. C. Avaliação do polissacarídeo da goma do cajueiro (Annacardium occidentale L.) como agente mucoadesivo e controlador da liberação em comprimidos matriciais. 2016. 54 f. Dissertação (Mestrado em Ciências Farmacêuticas) - Universidade Federal de Goiás, Goiânia, 2016. |
dc.identifier.uri.fl_str_mv |
http://repositorio.bc.ufg.br/tede/handle/tede/6766 |
dc.identifier.dark.fl_str_mv |
ark:/38995/00130000050kb |
identifier_str_mv |
Oliveira, A. C. Avaliação do polissacarídeo da goma do cajueiro (Annacardium occidentale L.) como agente mucoadesivo e controlador da liberação em comprimidos matriciais. 2016. 54 f. Dissertação (Mestrado em Ciências Farmacêuticas) - Universidade Federal de Goiás, Goiânia, 2016. ark:/38995/00130000050kb |
url |
http://repositorio.bc.ufg.br/tede/handle/tede/6766 |
dc.language.iso.fl_str_mv |
por |
language |
por |
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824936988196152412 |
dc.relation.confidence.fl_str_mv |
600 600 600 |
dc.relation.department.fl_str_mv |
6010281161524209375 |
dc.relation.cnpq.fl_str_mv |
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dc.rights.driver.fl_str_mv |
http://creativecommons.org/licenses/by-nc-nd/4.0/ info:eu-repo/semantics/openAccess |
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http://creativecommons.org/licenses/by-nc-nd/4.0/ |
eu_rights_str_mv |
openAccess |
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dc.publisher.none.fl_str_mv |
Universidade Federal de Goiás |
dc.publisher.program.fl_str_mv |
Programa de Pós-graduação em Ciências Farmacêuticas (FF) |
dc.publisher.initials.fl_str_mv |
UFG |
dc.publisher.country.fl_str_mv |
Brasil |
dc.publisher.department.fl_str_mv |
Faculdade Farmácia - FF (RG) |
publisher.none.fl_str_mv |
Universidade Federal de Goiás |
dc.source.none.fl_str_mv |
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bitstream.checksum.fl_str_mv |
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bitstream.checksumAlgorithm.fl_str_mv |
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 |
_version_ |
1815172562803490816 |