Simple jQuery Dropdowns
Please use this identifier to cite or link to this item: http://repository.li.mahidol.ac.th/dspace/handle/123456789/13974
Title: Enzymatically degradable nanoparticles of dextran esters as potential drug delivery systems
Authors: Kulthida Kaewprapan
Pranee Inprakhon
Emmanuelle Marie
Alain Durand
Mahidol University
Center of Excellence on Agricultural Biotechnology: (AG-BIO/PERDO-CHE)
Laboratoire de Chimie Physique Macromoleculaire
Keywords: Chemistry;Materials Science
Issue Date: 15-Apr-2012
Citation: Carbohydrate Polymers. Vol.88, No.3 (2012), 875-881
Abstract: Dextran decanoate esters with degrees of substitution (average molar ratio of ester functions to glucose repeat units) between 20 and 150% were used to form nanoparticles via nanoprecipitation technique. Particle size and colloidal stability of nanoparticles were found to depend on dextran concentration and degree of substitution. The colloidal stability of nanoparticle suspensions in sodium chloride solutions was improved by using a water-soluble dextran derivative as stabilizer. Enzymatic hydrolysis of ester bonds by porcine pancreatic lipase was demonstrated for highly modified dextran derivatives (up to DS = 150%). Complete degradation of low modified dextrans (DS up to 25%) by dextranase occurred within 7 days. Finally, encapsulation of lidocaine (as a model drug) into nanoparticles obtained with dextran esters (DS ranging between 21 and 150%) was investigated. © 2012 Elsevier Ltd. All rights reserved.
URI: https://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=84857922583&origin=inward
http://repository.li.mahidol.ac.th/dspace/handle/123456789/13974
ISSN: 01448617
Appears in Collections:Scopus 2011-2015

Files in This Item:
There are no files associated with this item.


Items in DSpace are protected by copyright, with all rights reserved, unless otherwise indicated.