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Formulation and evaluation of xanthan gum based aceclofenac tablets for colon targeted drug delivery / Formulação e avaliação de goma xantana baseados comprimidos Aceclofenac por câncer de cólon de entrega de drogas alvo
Ramasamy, Thiruganesh; Kandhasami, Uma Devi Subbaih; Ruttala, Himabindhu; Shanmugam, Suresh.
  • Ramasamy, Thiruganesh; Utah-Inha DDS & Advanced Therapeutics Research Center. Department of Bioengineering and Regenerative medicine. KR
  • Kandhasami, Uma Devi Subbaih; Vel's University. School of Pharmaceutical Sciences. Department of Pharmaceutics. Chennai. IN
  • Ruttala, Himabindhu; Pydah College of Pharmacy. Department of Pharmaceutics. Kakinada. IN
  • Shanmugam, Suresh; Vel's University. School of Pharmaceutical Sciences. Department of Pharmaceutics. Chennai. IN
Braz. j. pharm. sci ; 47(2): 299-311, Apr.-June 2011. ilus, tab
Article Dans Anglais | LILACS | ID: lil-595818
ABSTRACT
The objective of the present study is to develop a colon targeted drug delivery systems for Aceclofenac using xanthan gum as a carrier. In this study, multilayer coated system that is resistant to gastric and small intestinal conditions but can be easily degraded by colonic bacterial enzymes was designed to achieve effective colon delivery of Aceclofenac. The xanthan gum, the drug and the physical mixture were characterized by Fourier transform infrared spectroscopy (FTIR) and differential scanning calorimetry (DSC). All the formulations were evaluated for hardness, drug content uniformity and other physical properties. Release aspects of Aceclofenac in simulated gastrointestinal fluid and colonic fluid with enzymes were investigated. From these results, Eudragit coated system exhibited gastric and small intestinal resistance to the release of Aceclofenac. The rapid increase in release of Aceclofenac in SCF was revealed as due to the degradation of the xanthan gum membrane by bacterial enzymes. The designed system could be used potentially as a carrier for colon delivery of Aceclofenac by regulating drug release in stomach and the small intestine.
RESUMO
O presente estudo teve como objetivo o desenvolvimento de sistema de liberação cólon-alvo de aceclofenaco empregando goma xantana. Nesse trabalho, o revestimento de múltiplas camadas com característica de resistência às condições do intestino delgado além de gastrorresistência oferece como vantagem a rápida degradação desse sistema por enzimas bacterianas colônicas. Dessa forma, o planejamento de tal sistema possibilitou a liberação específica do aceclofenaco no cólon. A goma xantana e o fármaco, além da mistura física desses dois componentes, foram caracterizados por espectroscopia no infravermelho com transformada de Fourier (FTIR) e calorimetria diferencial exploratória (DSC). Todas as formulações foram avaliadas no que se refere à dureza, à uniformidade de conteúdo do fármaco além de outras propriedades físicas. Os perfis de liberação do aceclofenaco no fluido gástrico simulado e fluido colônico simulado contendo enzimas foram investigados. Os resultados revelaram que o sistema revestido com Eudragit® exibiu resistência gástrica e intestinal à liberação de aceclofenaco. O rápido aumento na liberação de aceclofenaco no fluido colônico simulado foi atribuido à degradação da goma xantana por enzimas bacterianas. O sistema apresenta aplicação potencial no desenvolvimento de produtos para a liberação cólon-alvo de aceclofenaco.
Sujets)


Texte intégral: Disponible Indice: LILAS (Amériques) Sujet Principal: Techniques in vitro / Pharmacocinétique / Chimie pharmaceutique / Tumeurs du côlon / Évaluation de médicament Type d'étude: Études d'évaluation langue: Anglais Texte intégral: Braz. j. pharm. sci Année: 2011 Type: Article Pays d'affiliation: Inde / Corée du Sud Institution/Pays d'affiliation: Pydah College of Pharmacy/IN / Utah-Inha DDS & Advanced Therapeutics Research Center/KR / Vel's University/IN

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Texte intégral: Disponible Indice: LILAS (Amériques) Sujet Principal: Techniques in vitro / Pharmacocinétique / Chimie pharmaceutique / Tumeurs du côlon / Évaluation de médicament Type d'étude: Études d'évaluation langue: Anglais Texte intégral: Braz. j. pharm. sci Année: 2011 Type: Article Pays d'affiliation: Inde / Corée du Sud Institution/Pays d'affiliation: Pydah College of Pharmacy/IN / Utah-Inha DDS & Advanced Therapeutics Research Center/KR / Vel's University/IN