An antibacterial and anti-oxidant hydrogel containing hyperbranched poly-L-lysine and tea polyphenols accelerates healing of infected wound

被引:9
|
作者
Wang, Jie [1 ]
Sun, Yiming [2 ]
Liu, Xiaoqing [1 ]
Kang, Yongyuan [1 ]
Cao, Wangbei [1 ]
Ye, Juan [2 ]
Gao, Changyou [1 ,3 ,4 ]
机构
[1] Zhejiang Univ, Dept Polymer Sci & Engn, MOE Key Lab Macromol Synth & Functionalizat, Hangzhou 310058, Peoples R China
[2] Zhejiang Univ, Affiliated Hosp 2, Eye Ctr, Sch Med, Hangzhou 310009, Peoples R China
[3] Shanxi Zheda Inst Adv Mat & Chem Engn, Taiyuan 030000, Shanxi, Peoples R China
[4] Zhejiang Univ, Shaoxing Inst, Ctr Healthcare Mat, Shaoxing 312099, Peoples R China
来源
BIOMATERIALS ADVANCES | 2024年 / 157卷
基金
中国国家自然科学基金;
关键词
Hydrogel; Wound dressing; Wound healing; Anti-oxidation; Antimicrobial; DRUG-DELIVERY; SKIN; PROLIFERATION; FABRICATION; RESISTANT; BACTERIA;
D O I
10.1016/j.bioadv.2023.213755
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
Both bacteria-infection and excessive inflammation delay the wound healing process and even create non-healing wound, thus it is highly desirable to endow the wound dressing with bactericidal and anti-oxidation properties. Herein an antibacterial and antioxidation hydrogel based on Carbomer 940 (CBM) and hydroxypropyl methyl cellulose (HPMC) loaded with tea polyphenols (TP) and hyperbranched poly-L-lysine (HBPL) was designed and fabricated. The hydrogel killed 99.9 % of methicillin-resistant Staphylococcus aureus (MRSA) and Escherichia coli (E. coli) at 107 CFU mL-1, and showed strong antioxidation against H2O2 and 2,2-di(4-tert-octylphenyl)-1-picryl-hydrazyl (DPPH) radicals without noticeable cytotoxicity in vitro. The CBM/HPMC/HBPL/TP hydrogel significantly shortened the inflammatory period of the MRSA-infected full-thickness skin wound of rats in vivo, with 2 orders of lower MRSA colonies compared with the blank control, and promoted the wound closure especially at the earlier stage. The inflammation was suppressed and the vascularization was promoted significantly as well, resulting in reduced pro-inflammatory factors including interleukin-6 (IL-6), interleukin-1 beta (IL-1 beta) and tumor necrosis factor-alpha (TNF-alpha), and increased anti-inflammatory factors such as interleukin-4 (IL-4) and interleukin-10 (IL-10).
引用
收藏
页数:12
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