Synthesis of stimuli-responsive chitosan-based hydrogels by Diels-Alder cross-linking 'click' reaction as potential carriers for drug administration

被引:70
作者
Guaresti, O. [1 ]
Garcia-Astrain, C. [1 ,3 ]
Aguirresarobe, R. H. [2 ]
Eceiza, A. [1 ]
Gabilondo, N. [1 ]
机构
[1] Univ Basque Country UPV EHU, Engn Coll Gipuzkoa, Dept Chem & Environm Engn, Mat Technol Grp, Plaza Europa 1, Donostia San Sebastian 20018, Spain
[2] Univ Basque Country UPV EHU, Dept Polymer Sci & Technol, POLYMAT, POB 1072, Donostia San Sebastian 20018, Spain
[3] Univ Strasbourg, UMR CNRS 7515, BioTeam ICPEES ECPM, 25 Rue Becquerel, F-67087 Strasbourg 2, France
关键词
Chitosan-based hydrogels; 'Click' chemistry; Diels-Alder cross-linking reaction; Stimuli-Responsive materials; Chloramphenicol; CHITOSAN/POLY(VINYL ALCOHOL) HYDROGELS; TISSUE ENGINEERING APPLICATIONS; HYALURONIC-ACID HYDROGELS; IN-VITRO DEGRADATION; CONTROLLED-RELEASE; MOLECULAR-WEIGHT; BIOMEDICAL APPLICATIONS; CONTROLLED DELIVERY; COMMERCIAL ENZYME; SUSTAINED-RELEASE;
D O I
10.1016/j.carbpol.2017.12.034
中图分类号
O69 [应用化学];
学科分类号
081704 ;
摘要
Stimuli-responsive chitosan-based hydrogels for biomedical applications using the Diels-Alder reaction were prepared. Furan modified chitosan (Cs-Fu) was cross-linked with polyetheramine derived bismaleimide at different equivalent ratios in order to determine the effect in the swelling and release properties on the final CsFu:BMI hydrogels. The Diels Alder cross-linking reaction was monitored by UV-vis spectroscopy and rheological measurements. Both the sol-gel transition value and the final storage modulus for the different formulations were similar and close to 40 min and 400 Pa, respectively. On the contrary, the swelling degree was found to be strongly dependent on the amount of bismaleimide, mainly in acidic medium, where the increased cross-linking reduced the swelling value in 25%, but maintaining the sustained drug release in the simulated gastrointestinal environment. Our study suggested that these DA-cross-linked chitosan hydrogels could be potential carriers for targeted drug administration.
引用
收藏
页码:278 / 286
页数:9
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