2019
DOI: 10.1080/1023666x.2018.1553348
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3D scaffolds prepared from acylated chitosan applicable in skin regeneration – synthesis and characterization

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Cited by 5 publications
(13 citation statements)
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“…Finally, bands at 2924 cm −1 and 2873 cm −1 corresponds to -CH-and -CH 2 -groups. The spectrum of the modified chitosan shows bands of significantly increased intensity at 2921 cm −1 and 2856 cm −1 , which proves acyl chains incorporation [28]. A new band at 1750 cm −1 can be noticed, which means that the acylation reaction occurred due to the formation of ester bonds between free hydroxyl groups of chitosan and carboxyl groups.…”
Section: Phenotype Studymentioning
confidence: 86%
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“…Finally, bands at 2924 cm −1 and 2873 cm −1 corresponds to -CH-and -CH 2 -groups. The spectrum of the modified chitosan shows bands of significantly increased intensity at 2921 cm −1 and 2856 cm −1 , which proves acyl chains incorporation [28]. A new band at 1750 cm −1 can be noticed, which means that the acylation reaction occurred due to the formation of ester bonds between free hydroxyl groups of chitosan and carboxyl groups.…”
Section: Phenotype Studymentioning
confidence: 86%
“…Chitosan (CS) acylation proceeded according to a previously described method using fatty acid chloride as an acylating agent [28]. Briefly, 0.5 g of the chitosan was placed in an acetone/TEA solution and irradiated for 30 min in a microwave reactor.…”
Section: Chitosan Acylationmentioning
confidence: 99%
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