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Chitosan coated Ca-alginate microparticles loaded with budesonide for delivery to the inflamed colonic mucosa.
Eur J Pharm Biopharm. 2008 Mar; 68(3):565-78.EJ

Abstract

Using a novel one-step spray-drying process uncoated and Eudragit S 100 coated chitosan-Ca-alginate microparticles efficiently loaded with budesonide (BDS), with bioadhesive and controlled release properties in GIT, were prepared. Microparticles were spherical with mean particle size of 4.05-5.36 microm, narrow unimodal distribution and positive surface charge. A greater extent of calcium chloride limited the swelling ratio of beads, while swelling behaviour of coated beads was mainly determined by properties of enteric coating. Comparing the release profiles of formulations, under different pH conditions, influence of polymer properties and concentration of cross-linker on the rate and extent of drug release was evident. Coating has successfully sustained release of BDS in buffers at pH 2.0 and 6.8, while providing potential for efficient release of BDS at pH 7.4. Release data kinetics indicated influence of erosion and biodegradation of polymer matrix on drug release from microparticles. Prepared formulations were stable for 12 months period at controlled ambient conditions. In conclusion coated microparticles prepared by one-step spray-drying procedure could be suitable candidates for oral delivery of BDS with controlled release properties for local treatment of inflammatory bowel diseases.

Authors+Show Affiliations

Institute of Pharmaceutical Technology, Ss. Cyril and Methodius University, Skopje, Macedonia.No affiliation info availableNo affiliation info available

Pub Type(s)

Journal Article
Research Support, Non-U.S. Gov't

Language

eng

PubMed ID

17651952

Citation

Simonoska Crcarevska, Maja, et al. "Chitosan Coated Ca-alginate Microparticles Loaded With Budesonide for Delivery to the Inflamed Colonic Mucosa." European Journal of Pharmaceutics and Biopharmaceutics : Official Journal of Arbeitsgemeinschaft Fur Pharmazeutische Verfahrenstechnik E.V, vol. 68, no. 3, 2008, pp. 565-78.
Simonoska Crcarevska M, Glavas Dodov M, Goracinova K. Chitosan coated Ca-alginate microparticles loaded with budesonide for delivery to the inflamed colonic mucosa. Eur J Pharm Biopharm. 2008;68(3):565-78.
Simonoska Crcarevska, M., Glavas Dodov, M., & Goracinova, K. (2008). Chitosan coated Ca-alginate microparticles loaded with budesonide for delivery to the inflamed colonic mucosa. European Journal of Pharmaceutics and Biopharmaceutics : Official Journal of Arbeitsgemeinschaft Fur Pharmazeutische Verfahrenstechnik E.V, 68(3), 565-78.
Simonoska Crcarevska M, Glavas Dodov M, Goracinova K. Chitosan Coated Ca-alginate Microparticles Loaded With Budesonide for Delivery to the Inflamed Colonic Mucosa. Eur J Pharm Biopharm. 2008;68(3):565-78. PubMed PMID: 17651952.
* Article titles in AMA citation format should be in sentence-case
TY - JOUR T1 - Chitosan coated Ca-alginate microparticles loaded with budesonide for delivery to the inflamed colonic mucosa. AU - Simonoska Crcarevska,Maja, AU - Glavas Dodov,Marija, AU - Goracinova,Katerina, Y1 - 2007/06/14/ PY - 2006/12/27/received PY - 2007/06/08/revised PY - 2007/06/09/accepted PY - 2007/7/27/pubmed PY - 2008/6/11/medline PY - 2007/7/27/entrez SP - 565 EP - 78 JF - European journal of pharmaceutics and biopharmaceutics : official journal of Arbeitsgemeinschaft fur Pharmazeutische Verfahrenstechnik e.V JO - Eur J Pharm Biopharm VL - 68 IS - 3 N2 - Using a novel one-step spray-drying process uncoated and Eudragit S 100 coated chitosan-Ca-alginate microparticles efficiently loaded with budesonide (BDS), with bioadhesive and controlled release properties in GIT, were prepared. Microparticles were spherical with mean particle size of 4.05-5.36 microm, narrow unimodal distribution and positive surface charge. A greater extent of calcium chloride limited the swelling ratio of beads, while swelling behaviour of coated beads was mainly determined by properties of enteric coating. Comparing the release profiles of formulations, under different pH conditions, influence of polymer properties and concentration of cross-linker on the rate and extent of drug release was evident. Coating has successfully sustained release of BDS in buffers at pH 2.0 and 6.8, while providing potential for efficient release of BDS at pH 7.4. Release data kinetics indicated influence of erosion and biodegradation of polymer matrix on drug release from microparticles. Prepared formulations were stable for 12 months period at controlled ambient conditions. In conclusion coated microparticles prepared by one-step spray-drying procedure could be suitable candidates for oral delivery of BDS with controlled release properties for local treatment of inflammatory bowel diseases. SN - 0939-6411 UR - https://www.unboundmedicine.com/medline/citation/17651952/Chitosan_coated_Ca_alginate_microparticles_loaded_with_budesonide_for_delivery_to_the_inflamed_colonic_mucosa_ DB - PRIME DP - Unbound Medicine ER -