A terpolymeric hydrogel of hyaluronate-hydroxyethyl acrylate-gelatin methacryloyl with tunable properties as biomaterial

被引:30
作者
Das, Dipankar [1 ,2 ]
Cho, Hana [3 ]
Kim, Nahye [2 ]
Thi Thu Hien Pham [2 ]
Kim, In Gul [3 ]
Chung, Eun-Jae [3 ]
Noh, Insup [1 ,2 ]
机构
[1] Seoul Natl Univ Sci & Technol, Dept Chem & Biomol Engn, Seoul 01811, South Korea
[2] Seoul Natl Univ Sci & Technol, Convergence Inst Biomed Engn & Biomat, Seoul 01811, South Korea
[3] Seoul Natl Univ Hosp, Dept Otorhinolaryngol, Coll Med, Seoul, South Korea
基金
新加坡国家研究基金会;
关键词
Bovine serum albumin; Dexamethasone; Drug delivery; Human chondrocytes; Hyaluronate; Hydrogel; CROSS-LINKED HYDROGEL; DRUG-DELIVERY; CONTROLLED-RELEASE; SUSTAINED-RELEASE; BLEND HYDROGEL; ACID HYDROGELS; IN-VITRO; SCAFFOLDS; DEXTRIN; CHITOSAN;
D O I
10.1016/j.carbpol.2018.12.020
中图分类号
O69 [应用化学];
学科分类号
081704 ;
摘要
Here, we report synthesis of a terpolymeric covalently crosslinked hydrogel of hyaluronate (HA) as biomaterial with elasticity, mechanical properties and cell interactions via conventional free radical polymerization technique. To provide elasticity and mechanical properties, 2-hydroxyethyl acrylate (HEA) was grafted in HA, while to tune cellular interactions, gelatin methacryloyl (GM) was used as crosslinker. The composition and probable structure of the terpolymer (HA-g-pHEA-x-GM) were analysed by FTIR, H-1 HR-MAS-NMR, and TGA analyses. The SEM and texture analyses of hydrogel showed interconnected micro-porous network and high mechanical properties, respectively. In vitro biocompatibility was studied against human chondrocytes, whereas, in vivo biocompatibility and tissue regeneration were confirmed using mouse model. The hydrogel releases model protein-bovine serum albumin, and corticosteroid drug-dexamethasone in a sustain way at pH 7.4 and 37 degrees C. Overall, the tunable mechanical properties, micro-porous network, and cytocompatibility of the HA-g-pHEA-x-GM hydrogel highlights its potential applicability in cartilage tissue engineering and drug delivery.
引用
收藏
页码:628 / 639
页数:12
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