2021
DOI: 10.1002/ddr.21804
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Therapeutic delivery with V‐amylose

Abstract: The helical structure of V-amylose offering a superior encapsulation affinity compared with the other polysaccharides, especially toward the amphiphilic or hydrophobic molecules; in addition to providing a higher resistance toward enzymatic hydrolysis support its applications as a potential drug delivery vehicle. Mainly, the glycosidic linkages and -CH 2groups forming the hydrophobic cavity of V-amylose helix, and the glycosyl hydroxyl groups constituting its hydrophilic periphery promote

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Cited by 17 publications
(5 citation statements)
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References 12 publications
(11 reference statements)
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“…The polysaccharides do not convert into acids at low temperatures, while in an alkaline solution, both the starch and cellulose thermochemically degrade to water-soluble compounds [64,65]. These properties support the colon-targeted release of the cargo drug molecules and prevent their premature release in the acidic pH of the stomach [66].…”
Section: Physicochemical Factorsmentioning
confidence: 94%
“…The polysaccharides do not convert into acids at low temperatures, while in an alkaline solution, both the starch and cellulose thermochemically degrade to water-soluble compounds [64,65]. These properties support the colon-targeted release of the cargo drug molecules and prevent their premature release in the acidic pH of the stomach [66].…”
Section: Physicochemical Factorsmentioning
confidence: 94%
“…The dicarbamate system linked to the lysine residue lining the enzyme active site, via carbonyl "O" atoms thereby forming a lysine adduct, which further interacts with the neighboring cysteine residues causing the crosslinking of the phosphate-binding site. [95][96][97][98]…”
Section: Benzoxazolone Derivatives As Pyrophosphate Mimics For Galnac...mentioning
confidence: 99%
“…Amylose has recently garnered great attention due to its tightly packed helical structure, physiological benevolence, biocompatibility, hydrophobic interior and hydrophilic exterior suitable for delivering various NSAIDs (non steroidal anti inflammatory drugs) and anti cancer drug molecules. [18] Amylose has low solubility in water and is easily retrogradable due to the presence of multiple hydrogen bonds between its hydroxyl groups that hampers its movement in aqueous solution. To overcome these obstacles, chemical modification is the most effective way to improve its structural and functional properties.…”
Section: Starchmentioning
confidence: 99%