A tough synthetic hydrogel with excellent post-loading of drugs for promoting the healing of infected wounds in vivo

被引:14
作者
Deng, Liwen [1 ,4 ]
Lu, Huidan [3 ]
Tu, Chenxi [2 ,4 ]
Zhou, Tong [4 ]
Cao, Wangbei [4 ]
Gao, Changyou [1 ,2 ,4 ]
机构
[1] Zhejiang Univ, Coll Biomed Engn & Instrument Sci, Hangzhou 310027, Peoples R China
[2] Shanxi Zheda Inst Adv Mat & Chem Engn, Taiyuan 030000, Peoples R China
[3] Zhejiang Univ, Sch Med, Affiliated Hosp 2, Hangzhou 310009, Peoples R China
[4] Zhejiang Univ, Dept Polymer Sci & Engn, MOE Key Lab Macromol Synth & Functionalizat, Hangzhou 310027, Peoples R China
来源
BIOMATERIALS ADVANCES | 2022年 / 134卷
关键词
Hydrogel; Post loading; Antibacteria; Wound healing; Inflammation; ANTIBACTERIAL; DRESSINGS; DELIVERY;
D O I
10.1016/j.msec.2021.112577
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
Bacterial infection is a major obstacle to the wound healing process. The hydrogel dressings with a simpler structure and good antibacterial and wound healing performance are appealing for clinical application. Herein, a robust hydro gel was synthesized from acrylamide (AM), acrylic acid (AA) and N,N???-methylene diacrylamide (MBA) via a redox initiating polymerization. The polymerization conditions were optimized to obtain the hydrogel with minimum unreacted monomers, which were 0.25% and 0.12% for AM and AA, respectively. The hydrogel had good mechanical strength, and could effectively resist damage by external forces and maintain a good macroscopic shape. It showed large water uptake capacity, and could post load a wide range of molecules via hydrogen bonding and electrostatic interaction. Loading of antibiotic doxycycline (DOX) enabled the hydrogel with good antibacterial activity against both Gram-positive bacteria and Gram-negative bacteria in vitro and in vivo. In a rat model of methicillin-resistant Staphylococcus aureus (MRSA)-infected full-thickness skin defect wound, the DOX-loaded hydrogel showed good therapeutic effect. It could significantly promote the wound closure, increased the collagen coverage area, down regulate the expressions of pro-inflammatory TNF-?? and IL-1?? factors, and up-regulate the expressions of antiinflammatory IL-4 factor and CD31 neovascularization factor.
引用
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页数:12
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