2017
DOI: 10.1016/j.ijbiomac.2017.03.077
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Synergistic effect of divalent cations in improving technological properties of cross-linked alginate beads

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Cited by 43 publications
(22 citation statements)
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“…As previously reported in our study [22], in fact, the co-presence of calcium (Ca 2+ ) and zinc (Zn 2+ ) could have a synergistic effect during the external ionotropic gelation, significantly improving the technological properties (i.e., encapsulation efficiency and drug release control) of the resulting cross-linked alginate beads. This effect is because of both the ability of Ca 2+ to establish quicker electrostatic interactions with guluronic groups and the ability of Zn 2+ to bond in covalent-like manner carboxylate groups of guluronic and mannuronic moieties of alginate.…”
Section: Introductionsupporting
confidence: 60%
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“…As previously reported in our study [22], in fact, the co-presence of calcium (Ca 2+ ) and zinc (Zn 2+ ) could have a synergistic effect during the external ionotropic gelation, significantly improving the technological properties (i.e., encapsulation efficiency and drug release control) of the resulting cross-linked alginate beads. This effect is because of both the ability of Ca 2+ to establish quicker electrostatic interactions with guluronic groups and the ability of Zn 2+ to bond in covalent-like manner carboxylate groups of guluronic and mannuronic moieties of alginate.…”
Section: Introductionsupporting
confidence: 60%
“…Although some studies have been focused on the production of floating alginate beads with calcium in the gelling solution, few data are available on the simultaneous use of two different cations as cross-linking agents [22,23]. Moreover, no results have been reported on the exploitation of two different cations in a double simultaneous gelation mechanism, that is, external, promoted by zinc ions in the gelling solution, and internal, promoted by calcium ions in prilling the feed solution.…”
Section: Introductionmentioning
confidence: 99%
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“…As a consequence, several innovative drug delivery systems have been developed to achieve a selective drug delivery to the inflamed tissues [6][7][8][9]. With this aim, several approaches can be followed, i.e., the use of prodrugs becoming active after the hydrolysis by specific colon enzymes [10], bioadhesive delivery systems [11], timed-dependent delivery systems [12] and drug coating with pH dependent polymers [13,14]. In this case, the use of pH-sensitive polymers protects the drug from the early release in the acidic pH of the stomach and small intestine, increasing the amount of active compound in the colon region.…”
Section: Introductionmentioning
confidence: 99%