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Bio-inspired catechol conjugation converts water-insoluble chitosan into a highly water-soluble, adhesive chitosan derivative for hydrogels and LbL assembly

Authors
Kim, KyuriRyu, Ji HyunLee, Dong YunLee, Haeshin
Issue Date
Jul-2013
Publisher
ROYAL SOC CHEMISTRY
Citation
BIOMATERIALS SCIENCE, v.1, no.7, pp.783 - 790
Indexed
SCIE
SCOPUS
Journal Title
BIOMATERIALS SCIENCE
Volume
1
Number
7
Start Page
783
End Page
790
URI
https://scholarworks.bwise.kr/hanyang/handle/2021.sw.hanyang/162370
DOI
10.1039/c3bm00004d
ISSN
2047-4830
Abstract
This report describes a simple method to prepare water-soluble chitosan derivative by conjugation of an enediol group, catechol. Chitosan functionalized with a catechol-containing compound, 3,4-dihydroxy-hydrocinnamic acid, by a carbodiimide coupling method resulted in chitosan-catechol conjugates. This one-step chemical modification of high-molecular-weight chitosan (approximately 100 kDa) dramatically increased the water solubility of the chitosan derivative to 60 mg mL(-1) at pH 7.0. The degree of catechol conjugation was found critical in determining the solubility. The chitosan-catechol conjugates are not only water-soluble but are adhesive, due to the intrinsic adhesive properties of catechol. Also, the water-soluble chitosan derivative allows one to directly form chitosan hydrogel in neutral buffer solutions. The utility of both the water solubility and the adhesive property of the chitosan-catechol was demonstrated by the effective layer-by-layer assembly on substrates. The water-soluble chitosan-catechol is expected to be useful in many areas of surface functionalization, drug delivery, tissue engineering, and tissue adhesives.
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