Desenvolvimento de comprimidos contendo pellets revestidos para liberação cólon específica de cetoprofeno

Detalhes bibliográficos
Autor(a) principal: Alencar, Rodrigo Gomes de
Data de Publicação: 2014
Tipo de documento: Dissertação
Idioma: por
Título da fonte: Repositório Institucional da UFG
Texto Completo: http://repositorio.bc.ufg.br/tede/handle/tede/4020
Resumo: Ketoprofen is a nonsteroidal anti-inflammatory drug used for the treatment of mild to moderate pain in chronic inflammatory conditions. Due to its superior potency ketoprofen can be used in the treatment of inflammatory bowel disease (IBD). The treatment of IBD becomes safer and more effective when the drug is incorporated into colon-specific drug delivery systems. Pellets are multiparticulate solid dosage forms extensively investigated as colon-specific drug delivery systems. Pellets can be introduced into capsules or compressed into tablets. The industrial production of tablets containing pellets has several advantages when compared to the production of capsules. However, the compression of the pellets should not affect the release of the drug and the tablets should quickly disintegrate following administration. Therefore, the aim of this study was to develop tablets containing ketoprofen coated pellets for colon-specific drug release. For this, pellets were produced by extrusion and spheronization technique containing 40% (w / w) ketoprofen. Ketoprofen pellets obtained were coated with two different pH - dependent polymers derived from methacrylic acid (Opadry ® k 94 or Eudragit ® FS 30D) with weight gains of 10 or 20% (w / w). The coated pellets were then compressed under different pellets’ amounts and different compression forces. An extra- granular mixture of lactose and microcrystalline cellulose was used as compression aid. The in vitro release of ketoprofen from the systems obtained was evaluated in Bio Dis ® apparatus. The morphological and physical properties of pellets and tablets were assessed. The Eudragit ® FS 30 D coated pellets with weight gains of 10 or 20% showed higher efficiency of colon-specific delivery (94 %), however, the drug was released slowly and incompletely in conditions mimicking the pH of the colonic region. After compression of the pellets, the efficiency of colon – specific drug delivery was lowered after compression (between 20% and 61%, depending on the formulation). The lowest decrease of colon specific efficiency was observed in formulations containing lower amount of pellets, which also produced disintegrating matrices with potential for use in the topical treatment of IBD.
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spelling Marreto, Ricardo Neveshttp://lattes.cnpq.br/6127043775208484Marreto, Ricardo NevesAraújo, Adriano Antunes de SouzaTaveira, Stephânia Fleuryhttp://lattes.cnpq.br/8958489303277830Alencar, Rodrigo Gomes de2015-01-30T12:58:45Z2014-04-25ALENCAR, Rodrigo Gomes de. Desenvolvimento de comprimidos contendo pellets revestidos para liberação cólon específica de cetoprofeno. 2014. 75 f. Dissertação (Mestrado em Ciências Farmacêuticas) - Universidade Federal de Goiás, Goiânia, 2014.http://repositorio.bc.ufg.br/tede/handle/tede/4020Ketoprofen is a nonsteroidal anti-inflammatory drug used for the treatment of mild to moderate pain in chronic inflammatory conditions. Due to its superior potency ketoprofen can be used in the treatment of inflammatory bowel disease (IBD). The treatment of IBD becomes safer and more effective when the drug is incorporated into colon-specific drug delivery systems. Pellets are multiparticulate solid dosage forms extensively investigated as colon-specific drug delivery systems. Pellets can be introduced into capsules or compressed into tablets. The industrial production of tablets containing pellets has several advantages when compared to the production of capsules. However, the compression of the pellets should not affect the release of the drug and the tablets should quickly disintegrate following administration. Therefore, the aim of this study was to develop tablets containing ketoprofen coated pellets for colon-specific drug release. For this, pellets were produced by extrusion and spheronization technique containing 40% (w / w) ketoprofen. Ketoprofen pellets obtained were coated with two different pH - dependent polymers derived from methacrylic acid (Opadry ® k 94 or Eudragit ® FS 30D) with weight gains of 10 or 20% (w / w). The coated pellets were then compressed under different pellets’ amounts and different compression forces. An extra- granular mixture of lactose and microcrystalline cellulose was used as compression aid. The in vitro release of ketoprofen from the systems obtained was evaluated in Bio Dis ® apparatus. The morphological and physical properties of pellets and tablets were assessed. The Eudragit ® FS 30 D coated pellets with weight gains of 10 or 20% showed higher efficiency of colon-specific delivery (94 %), however, the drug was released slowly and incompletely in conditions mimicking the pH of the colonic region. After compression of the pellets, the efficiency of colon – specific drug delivery was lowered after compression (between 20% and 61%, depending on the formulation). The lowest decrease of colon specific efficiency was observed in formulations containing lower amount of pellets, which also produced disintegrating matrices with potential for use in the topical treatment of IBD.O cetoprofeno é um antiinflamatório não esteroidal usado para o tratamento de dores leves a moderadas, em condições inflamatórias crônicas. Devido a sua elevada potência antiinflamatória, o cetoprofeno pode ser aproveitado no tratamento das doenças inflamatórias intestinais (DII). O tratamento das DII se torna mais seguro e eficaz quando o fármaco é incorporado em sistemas de liberação cólon-específica. Pellets são formas farmacêuticas multiparticuladas bastante investigadas como sistemas de liberação cólon-específica. Após sua produção, os pellets podem ser inseridos em cápsulas ou comprimidos. A produção industrial de comprimidos contendo pellets apresenta inúmeras vantagens quando comparada ao processo de enchimento de cápsulas. No entanto, a compressão dos pellets não deve afetar as características de liberação do fármaco e os comprimidos formados devem se desintegrar rapidamente. Dessa forma, o objetivo deste trabalho foi desenvolver comprimidos contendo pellets revestidos para liberação cólon-específica de cetoprofeno. Para tanto, foram produzidos pellets contendo 40% (p/p) de cetoprofeno e celulose microcristalina pela técnica de extrusão e esferonização. Os pellets de cetoprofeno obtidos foram revestidos com dois diferentes polímeros pH-dependentes, ambos derivados do ácido metacrílico (Opadry ® 94 k ou Eudragit ® FS 30) com ganhos de massa 10 ou 20% (p/p). Os pellets revestidos foram então comprimidos com diferentes cargas de pellets e submetidos a diferentes forças de compressão, utilizando como adjuvante extra-pellets uma mistura granulada de lactose e celulose microcristalina. A liberação in vitro do cetoprofeno a partir das formas farmacêuticas obtidas foi avaliada em dissolutor Bio Dis aparato III. As caracterizações morfológicas e físicas dos pellets e comprimidos foram conduzidas. Os pellets obtidos por revestimento com Eudragit ® FS 30 D, com ganhos de massa de 10 ou 20%, mostraram elevada eficiência de liberação cólon-específica in vitro (até 94%), no entanto, o fármaco foi liberado de forma lenta e incompleta em meio com pH similar ao encontrado na região colônica. Após a compressão dos pellets, os valores de eficiência de liberação cólon-específica sofreram reduções entre 20% e 61%. A menor diminuição da eficiência de liberação cólon-específica foi observada nas formulações contendo a menor carga de pellets, as quais deram origem à matrizes desintegráveis com potencial para utilização no tratamento tópico das DII.Submitted by Cássia Santos (cassia.bcufg@gmail.com) on 2015-01-30T10:47:22Z No. of bitstreams: 2 license_rdf: 23148 bytes, checksum: 9da0b6dfac957114c6a7714714b86306 (MD5) Dissertação - Rodrigo Gomes de Alencar - 2014.pdf: 13066901 bytes, checksum: 15e26e7a3dde863c6267ef54f83385be (MD5)Approved for entry into archive by Luciana Ferreira (lucgeral@gmail.com) on 2015-01-30T12:58:45Z (GMT) No. of bitstreams: 2 license_rdf: 23148 bytes, checksum: 9da0b6dfac957114c6a7714714b86306 (MD5) Dissertação - Rodrigo Gomes de Alencar - 2014.pdf: 13066901 bytes, checksum: 15e26e7a3dde863c6267ef54f83385be (MD5)Made available in DSpace on 2015-01-30T12:58:45Z (GMT). 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dc.title.eng.fl_str_mv Desenvolvimento de comprimidos contendo pellets revestidos para liberação cólon específica de cetoprofeno
dc.title.alternative.eng.fl_str_mv Development of tablets contain coated pellets for colon specific release of ketoprofen
title Desenvolvimento de comprimidos contendo pellets revestidos para liberação cólon específica de cetoprofeno
spellingShingle Desenvolvimento de comprimidos contendo pellets revestidos para liberação cólon específica de cetoprofeno
Alencar, Rodrigo Gomes de
Extrusão
Esferonização
Compressão de pellets revestidos
Cetoprofeno
Polímeros acrílicos
Revestimento de pellets
Extrusion
Spheronization
Compression of coated pellets
Ketoprofen
Acrylic polymers
Coating of pellets
Solid multiparticulate systems
FARMACOLOGIA::FARMACOLOGIA GERAL
title_short Desenvolvimento de comprimidos contendo pellets revestidos para liberação cólon específica de cetoprofeno
title_full Desenvolvimento de comprimidos contendo pellets revestidos para liberação cólon específica de cetoprofeno
title_fullStr Desenvolvimento de comprimidos contendo pellets revestidos para liberação cólon específica de cetoprofeno
title_full_unstemmed Desenvolvimento de comprimidos contendo pellets revestidos para liberação cólon específica de cetoprofeno
title_sort Desenvolvimento de comprimidos contendo pellets revestidos para liberação cólon específica de cetoprofeno
author Alencar, Rodrigo Gomes de
author_facet Alencar, Rodrigo Gomes 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 Araújo, Adriano Antunes de Souza
dc.contributor.referee3.fl_str_mv Taveira, Stephânia Fleury
dc.contributor.authorLattes.fl_str_mv http://lattes.cnpq.br/8958489303277830
dc.contributor.author.fl_str_mv Alencar, Rodrigo Gomes de
contributor_str_mv Marreto, Ricardo Neves
Marreto, Ricardo Neves
Araújo, Adriano Antunes de Souza
Taveira, Stephânia Fleury
dc.subject.por.fl_str_mv Extrusão
Esferonização
Compressão de pellets revestidos
Cetoprofeno
Polímeros acrílicos
Revestimento de pellets
topic Extrusão
Esferonização
Compressão de pellets revestidos
Cetoprofeno
Polímeros acrílicos
Revestimento de pellets
Extrusion
Spheronization
Compression of coated pellets
Ketoprofen
Acrylic polymers
Coating of pellets
Solid multiparticulate systems
FARMACOLOGIA::FARMACOLOGIA GERAL
dc.subject.eng.fl_str_mv Extrusion
Spheronization
Compression of coated pellets
Ketoprofen
Acrylic polymers
Coating of pellets
Solid multiparticulate systems
dc.subject.cnpq.fl_str_mv FARMACOLOGIA::FARMACOLOGIA GERAL
description Ketoprofen is a nonsteroidal anti-inflammatory drug used for the treatment of mild to moderate pain in chronic inflammatory conditions. Due to its superior potency ketoprofen can be used in the treatment of inflammatory bowel disease (IBD). The treatment of IBD becomes safer and more effective when the drug is incorporated into colon-specific drug delivery systems. Pellets are multiparticulate solid dosage forms extensively investigated as colon-specific drug delivery systems. Pellets can be introduced into capsules or compressed into tablets. The industrial production of tablets containing pellets has several advantages when compared to the production of capsules. However, the compression of the pellets should not affect the release of the drug and the tablets should quickly disintegrate following administration. Therefore, the aim of this study was to develop tablets containing ketoprofen coated pellets for colon-specific drug release. For this, pellets were produced by extrusion and spheronization technique containing 40% (w / w) ketoprofen. Ketoprofen pellets obtained were coated with two different pH - dependent polymers derived from methacrylic acid (Opadry ® k 94 or Eudragit ® FS 30D) with weight gains of 10 or 20% (w / w). The coated pellets were then compressed under different pellets’ amounts and different compression forces. An extra- granular mixture of lactose and microcrystalline cellulose was used as compression aid. The in vitro release of ketoprofen from the systems obtained was evaluated in Bio Dis ® apparatus. The morphological and physical properties of pellets and tablets were assessed. The Eudragit ® FS 30 D coated pellets with weight gains of 10 or 20% showed higher efficiency of colon-specific delivery (94 %), however, the drug was released slowly and incompletely in conditions mimicking the pH of the colonic region. After compression of the pellets, the efficiency of colon – specific drug delivery was lowered after compression (between 20% and 61%, depending on the formulation). The lowest decrease of colon specific efficiency was observed in formulations containing lower amount of pellets, which also produced disintegrating matrices with potential for use in the topical treatment of IBD.
publishDate 2014
dc.date.issued.fl_str_mv 2014-04-25
dc.date.accessioned.fl_str_mv 2015-01-30T12:58:45Z
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 ALENCAR, Rodrigo Gomes de. Desenvolvimento de comprimidos contendo pellets revestidos para liberação cólon específica de cetoprofeno. 2014. 75 f. Dissertação (Mestrado em Ciências Farmacêuticas) - Universidade Federal de Goiás, Goiânia, 2014.
dc.identifier.uri.fl_str_mv http://repositorio.bc.ufg.br/tede/handle/tede/4020
identifier_str_mv ALENCAR, Rodrigo Gomes de. Desenvolvimento de comprimidos contendo pellets revestidos para liberação cólon específica de cetoprofeno. 2014. 75 f. Dissertação (Mestrado em Ciências Farmacêuticas) - Universidade Federal de Goiás, Goiânia, 2014.
url http://repositorio.bc.ufg.br/tede/handle/tede/4020
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language por
dc.relation.program.fl_str_mv 824936988196152412
dc.relation.confidence.fl_str_mv 600
600
600
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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
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http://repositorio.bc.ufg.br/tede/bitstreams/b1c6fba9-359c-4c06-a5a4-56cba028138c/download
http://repositorio.bc.ufg.br/tede/bitstreams/be27f7ee-70af-4cf7-b185-dddd9a825014/download
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repository.name.fl_str_mv Repositório Institucional da UFG - Universidade Federal de Goiás (UFG)
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