Preparation, characterization and in vitro digestibility of gellan and chitosan-gellan microgels.
Autor: | Vilela JAP; Department of Food Engineering, School of Food Engineering, University of Campinas (UNICAMP), R. Monteiro Lobato, 80, 13083-862 Campinas, SP, Brazil., Perrechil FA; Department of Food Engineering, School of Food Engineering, University of Campinas (UNICAMP), R. Monteiro Lobato, 80, 13083-862 Campinas, SP, Brazil., Picone CSF; Department of Food Engineering, School of Food Engineering, University of Campinas (UNICAMP), R. Monteiro Lobato, 80, 13083-862 Campinas, SP, Brazil., Sato ACK; Department of Food Engineering, School of Food Engineering, University of Campinas (UNICAMP), R. Monteiro Lobato, 80, 13083-862 Campinas, SP, Brazil., Cunha RLD; Department of Food Engineering, School of Food Engineering, University of Campinas (UNICAMP), R. Monteiro Lobato, 80, 13083-862 Campinas, SP, Brazil. Electronic address: rosiane@fea.unicamp.br. |
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Jazyk: | angličtina |
Zdroj: | Carbohydrate polymers [Carbohydr Polym] 2015 Mar 06; Vol. 117, pp. 54-62. Date of Electronic Publication: 2014 Sep 26. |
DOI: | 10.1016/j.carbpol.2014.09.019 |
Abstrakt: | Gellan microgels with potential application in delivery systems were obtained by physically cross-linked gellan gum. The microgels were produced by atomization followed by ionotropic gelation using CaCl2 (gellan/Ca) or KCl (gellan/K) as hardening agent and part of them were coated with chitosan in order to improve their resistance to gastric digestion. Size distribution, morphology and zeta potential of microgels were evaluated before and after in vitro digestion process. The long term stability was also evaluated. Spherical microparticles were obtained at gellan concentration above 0.6% w/w, showing average size among 70-120 μm. Most of the coated and uncoated microgels showed stability in aqueous media, except the uncoated gellan/K microgel. The in vitro digestion evaluation showed that all particles maintained their size and shape after the gastric digestion step. However, the enteric digestion caused disintegration of microgels indicating their potential application for enteric delivery systems. The chitosan-coated microgels showed lower degree of fragmentation when compared to the uncoated microgels, indicating that the coating process enable a better control of microgels releasing properties during the enteric digestion. (Copyright © 2014 Elsevier Ltd. All rights reserved.) |
Databáze: | MEDLINE |
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