Facile Preparation of Biodegradable Glycol Chitosan Hydrogels Using Divinyladipate as a Crosslinker
- Authors
- Kim, Beob Soo; Yeo, Tae Yun; Yun, Yeon Hee; Lee, Byung Kook; Cho, Yong Woo; Han, Sung Soo
- Issue Date
- Oct-2009
- Publisher
- POLYMER SOC KOREA
- Keywords
- chitosan; hydrogels; divinyladipate; biodegradable; pH-sensitive
- Citation
- MACROMOLECULAR RESEARCH, v.17, no.10, pp.734 - 738
- Indexed
- SCIE
SCOPUS
KCI
- Journal Title
- MACROMOLECULAR RESEARCH
- Volume
- 17
- Number
- 10
- Start Page
- 734
- End Page
- 738
- URI
- https://scholarworks.bwise.kr/erica/handle/2021.sw.erica/40845
- DOI
- 10.1007/BF03218607
- ISSN
- 1598-5032
- Abstract
- Biodegradable, pH-sensitive, glycol chitosan (GC) hydrogels were prepared using divinyl adipate (DVA) as a crosslinker and acetic acid as a catalyst. DVA has highly reactive double vinyl ester groups and GC contains a high density of hydroxyl groups, with two in every glucosamine unit. The transesterification reaction between vinyl esters and hydroxyl groups produced crosslinked GC hydrogels. The initial crosslinking reaction was monitored by measuring the viscosity of the reaction mixture. When DVA was added to the GC solution and heated to 50 degrees C, the viscosity of the GC solution gradually increased, implying a crosslinking reaction and hydrogel formation. A new peak from the ester group was observed in the FTIR spectra of the GC hydrogels, confirming the crosslinking reaction. The synthesized GC hydrogel showed pH-dependent water absorbency, mainly due to the presence of amine groups (-NH2) at the C-2 position of the glucosamine unit of GC. The water absorbency greatly increased at acidic pH and slightly decreased at alkaline pH. The GC hydrogel gradually degraded in 37 degrees C water due to hydrolysis of the ester bonds, which were intermolecular crosslinking sites. A red dye, 5-carboxyltetramethyl-rhodamine (CTMR), was entrapped in the GC hydrogels as a model compound. CTMR was released from GC hydrogels in two steps: an initial burst release mainly due to desorption and diffusion, and a second sustained release possibly due to gradual degradation.
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