Thermogelling chitosan-based polymers for the treatment of oral mucosa ulcers

被引:57
作者
Luo, Zheng [1 ,2 ]
Xue, Kun [3 ]
Zhang, Xikui [3 ]
Lim, Jason Y. C. [3 ]
Lai, Xiyu [1 ,2 ]
Young, David James [4 ]
Zhang, Zhong-Xing [3 ]
Wu, Yun-Long [1 ,2 ]
Loh, Xian Jun [3 ,5 ]
机构
[1] Xiamen Univ, Fujian Prov Key Lab Innovat Drag Target Res, Sch Pharmaceut Sci, Xiamen 361102, Peoples R China
[2] Xiamen Univ, State Key Lab Cellular Stress Biol, Sch Pharmaceut Sci, Xiamen 361102, Peoples R China
[3] ASTAR, Inst Mat Res & Engn, 2 Fusionopolis Way,Innovis 08-03, Singapore 138634, Singapore
[4] Charles Darwin Univ, Coll Engn Informat Technol & Environm, Darwin, NT 0909, Australia
[5] Quanzhou Normal Univ, Coll Chem Engn & Mat Sci, Quanzhou 362000, Peoples R China
关键词
RECURRENT APHTHOUS ULCERS; INJECTABLE HYDROGELS; HYALURONIC-ACID; PHYSICAL HYDROGELS; LINGUAL HEMOSTASIS; WOUND DRESSINGS; POLY(N-ISOPROPYLACRYLAMIDE); COPOLYMERS; GLYCOL); GEL;
D O I
10.1039/c9bm01754b
中图分类号
TB3 [工程材料学]; R318.08 [生物材料学];
学科分类号
0805 ; 080501 ; 080502 ;
摘要
Current treatments for oral mucosa-related ulcers use drugs to relieve pain and promote healing, but rarely consider drug resistance to bacterial infection in the microenvironment of the oral cavity or the prevention of bleeding from gingival mucosa ulcers. We herein report an injectable, thermogelling chitosan-based system to address these concerns. An aqueous solution of chitosan-based conjugates (chitosan-g-poly(N-isopropylacrylamide) [CS-g-PNIPAAM] including 1a [CS-g-PNIPAAM with less PNIPAAM] and 1b [CS-g-PNIPAAM with more PNIPAAM], and chitosan-g-poly(N-isopropylacrylamide)-g-polyacrylamide [CS-g-PNIPAAM-g-PAM] 3) could reversibly form semi-solid gels at physiological temperatures for easy application to oral cavity ulcer sites by injection. The chitosan-based conjugate thermogels prepared could inhibit both Gram-positive and Gram-negative bacteria and the two with higher chitosan and poly(N-isopropylacrylamide) contents (1a and 1b) promoted proliferation of gingival fibroblasts in vitro. These two thermogels also exhibited improved blood clotting in an in vivo rat study. Thermogels 1a and 1b effectively promoted ulcer healing and shortened ulcer healing times in an oral gingival mucosa ulcer model using Sprague Dawley (SD) rats. These thermogels showed no obvious toxicity to the main organs of SD rats undergoing gingival ulcer treatment. These results suggest that this antibacterial biomaterial could be a promising injectable therapeutic agent for the treatment for oral mucosa ulcers.
引用
收藏
页码:1364 / 1379
页数:16
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