In vitro drug permeation from chitosan pellets


Autoria(s): Ferrari, Priscileila C.; Souza, Fagner M.; Giorgetti, Leandro; Oliveira, Giselle F.; Chaud, Marco V.; Ferraz, Humberto G.; Evangelista, Raul Cesar
Contribuinte(s)

Universidade Estadual Paulista (UNESP)

Data(s)

20/05/2014

20/05/2014

01/03/2012

Resumo

Coordenação de Aperfeiçoamento de Pessoal de Nível Superior (CAPES)

The purpose of this study was to prepare and characterize coated pellets for controlled drug delivery. The influence of chitosan (CS) in pellets was evaluated by swelling, in vitro drug release and intestinal permeation assays. Pellets were coated with an enteric polymer, Kollicoat (R) MAE 30 DP, in a fluidized-bed apparatus and the coating formulations were based on a factorial design. Metronidazole (MT) released from coated and uncoated pellets were assessed by dissolution method using Apparatus I. Intestinal permeation was evaluated by everted intestinal sac model in rats, used to study the absorption of MT from coated pellets containing CS or not through the intestinal tissue. Although the film coating avoided drug dissolution in gastric medium, the overall drug release and intestinal permeation were dependent on the presence of CS. Thus, pellets containing CS show potential as a system for controlled drug delivery. (C) 2011 Elsevier Ltd. All rights reserved.

Formato

2526-2531

Identificador

http://dx.doi.org/10.1016/j.carbpol.2011.11.027

Carbohydrate Polymers. Oxford: Elsevier B.V., v. 87, n. 4, p. 2526-2531, 2012.

0144-8617

http://hdl.handle.net/11449/7796

10.1016/j.carbpol.2011.11.027

WOS:000299969800022

Idioma(s)

eng

Publicador

Elsevier B.V.

Relação

Carbohydrate Polymers

Direitos

closedAccess

Palavras-Chave #Pellets #Chitosan #Enteric coating #Metronidazole #Controlled drug delivery #Everted intestinal sac model
Tipo

info:eu-repo/semantics/article