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Please use this identifier to cite or link to this item: http://repository.li.mahidol.ac.th/dspace/handle/123456789/23055
Title: Chitosan drug binding by ionic interaction
Authors: Yaowalak Boonsongrit
Ampol Mitrevej
Bernd W. Mueller
Mahidol University
Christian-Albrechts-Universitat zu Kiel
Keywords: Biochemistry, Genetics and Molecular Biology;Pharmacology, Toxicology and Pharmaceutics
Issue Date: 1-Apr-2006
Citation: European Journal of Pharmaceutics and Biopharmaceutics. Vol.62, No.3 (2006), 267-274
Abstract: Three model drugs (insulin, diclofenac sodium, and salicylic acid) with different pI or pKa were used to prepare drug-chitosan micro/nanoparticles by ionic interaction. Physicochemical properties and entrapment efficiencies were determined. The amount of drug entrapped in the formulation influences zeta potential and surface charge of the micro/nanoparticles. A high entrapment efficiency of the micro/nanoparticles could be obtained by careful control of formulation pH. The maximum entrapment efficiency did not occur in the highest ionization range of the model drugs. The high burst release of drugs from chitosan micro/nanoparticles was observed regardless of the pH of dissolution media. It can be concluded that the ionic interaction between drug and chitosan is low and too weak to control the drug release.
URI: https://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=33644827869&origin=inward
http://repository.li.mahidol.ac.th/dspace/handle/123456789/23055
ISSN: 09396411
Appears in Collections:Scopus 2006-2010

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