Skip to Content
Merck
  • Development and in vitro evaluation of coated pellets containing chitosan to potential colonic drug delivery.

Development and in vitro evaluation of coated pellets containing chitosan to potential colonic drug delivery.

Carbohydrate polymers (2012-10-10)
Priscileila Colerato Ferrari, Fagner Magalhães Souza, Leandro Giorgetti, Giselle Faria Oliveira, Humberto Gomes Ferraz, Marco Vinícius Chaud, Raul Cesar Evangelista
ABSTRACT

In this work pellets containing chitosan for colonic drug delivery were developed. The influence of the polysaccharide in the pellets was evaluated by swelling, drug dissolution and intestinal permeation studies. Drug-loaded pellets containing chitosan as swellable polymer were coated with an inner layer of Kollicoat(®) SR 30 D and an outer layer of the enteric polymer Kollicoat(®) MAE 30 DP in a fluidized-bed apparatus. Metronidazole released from pellets was assessed using Bio-Dis dissolution method. Swelling, drug release and intestinal permeation were dependent on the chitosan and the coating composition. The drug release data fitted well with the Weibull equation, indicating that the drug release was controlled by diffusion, polymer relaxation and erosion occurring simultaneously. The film coating was found to be the main factor controlling the drug release and the chitosan controlling the drug intestinal permeation. Coated pellets containing chitosan show great potential as a system for drug delivery to the colon.

MATERIALS
Product Number
Brand
Product Description

Sigma-Aldrich
Kollicoat® SR 30 D, 28.5-31.5% solids basis
Poly(vinyl acetate) dispersion 30 per cent, European Pharmacopoeia (EP) Reference Standard
Sigma-Aldrich
Poly(vinyl acetate), average Mw ~500,000 by GPC
Sigma-Aldrich
Poly(vinyl acetate), average Mw ~100,000 by GPC, beads