2019
DOI: 10.1016/j.jbiotec.2018.11.005
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Encapsulated drug system based on the gels obtained from callus cultures modified pectins

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Cited by 17 publications
(10 citation statements)
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“…Na CMC, gelatin, and pectin have also been widely applied as drug‐delivery carriers, particularly to modify the release of drugs, including prednisolone . However, there has been no investigation into the bioavailability of prednisolone presented as a physical mix with the three polymers in combination.…”
Section: Discussionmentioning
confidence: 99%
“…Na CMC, gelatin, and pectin have also been widely applied as drug‐delivery carriers, particularly to modify the release of drugs, including prednisolone . However, there has been no investigation into the bioavailability of prednisolone presented as a physical mix with the three polymers in combination.…”
Section: Discussionmentioning
confidence: 99%
“…The presence of non-esterified acid residues promotes gelling in the presence of divalent ions, e.g., Ca 2+ , which results in the formation of the structure described by the eggbox model [2][3][4][5]. In the case of pectins with an average molecular mass above 300 kDa, the formed gels are characterized by a dense, compact structure, which determines their high mechanical strength, including breaking strength [6,7]. The presence of simple sugars in the branched structure of pectins may negatively affect gelation, they constitute a hindrance to the formation of bonds between acid residues and Ca 2+ ions [8].…”
Section: Introductionmentioning
confidence: 99%
“…Internal gelation consists of mixing a polymer solution with a slightly soluble salt; this mixture is then acidified in order to gradually release calcium ions, and gelling occurs in the entire volume of the mixture [5,9,10]. On the other hand, in the external gelation process, a polymer solution is added (usually dropwise) to a solution containing easily soluble calcium salts (e.g., calcium chloride); due to the high availability of calcium ions, gelation occurs almost immediately [4,7,[11][12][13][14]. The external gelation method allows to obtain a stronger gel with a more compact structure than internal gelation; moreover, it occurs much faster, and therefore it is used in the production of small particles, gel beads, while internal gelation is used to produce gels with larger dimensions [2,10].…”
Section: Introductionmentioning
confidence: 99%
“…CaP gels have been widely used in drug delivery systems, 7,8 or in the microencapsulation of food additives and bioactive compounds, 9‐11 because of their non‐toxic, highly biocompatible, mechanically strong and acid‐stable characteristics 3 . Using conventional methods, CaP gels are formed by calcium‐induced inotropic gelation of LMP 4 .…”
Section: Introductionmentioning
confidence: 99%
“…4 The CaP gel formation process has been explained structurally as an egg-box model, which is derived from the strong Ca 2+ -bridged dimers and weak interdimer associations formed by the electrostatic interactions between divalent ions (Ca 2+ ) and galacturonate blocks. 5,6 CaP gels have been widely used in drug delivery systems, 7,8 or in the microencapsulation of food additives and bioactive compounds, [9][10][11] because of their non-toxic, highly biocompatible, mechanically strong and acid-stable characteristics. 3 Using conventional methods, CaP gels are formed by calcium-induced inotropic gelation of LMP.…”
Section: Introductionmentioning
confidence: 99%