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Synergistical Starvation and Chemo-Dynamic Therapy for Combating Multidrug-Resistant Bacteria and Accelerating Diabetic Wound Healing
被引:56
|作者:
Li, Danxia
[1
]
Chen, Tao
[2
]
Zhang, Yanfang
[2
]
Xu, Yuanhong
[1
,2
]
Niu, Haitao
[1
]
机构:
[1] Qingdao Univ, Affiliated Hosp, Dept Urol, Qingdao 266003, Peoples R China
[2] Qingdao Univ, Coll Life Sci, Inst Biomed Engn, Qingdao 266071, Peoples R China
基金:
中国国家自然科学基金;
关键词:
antibacteria;
cascaded catalytic systems;
diabetic wound healing;
metal-organic frameworks;
nanoreactors;
METAL-ORGANIC FRAMEWORKS;
GLUCOSE-OXIDASE;
SYSTEM;
D O I:
10.1002/adhm.202100716
中图分类号:
R318 [生物医学工程];
学科分类号:
0831 ;
摘要:
The application of the antibiotic drug has dramatically decreased the infection and promoted the development of surgery, but drug-resistant bacteria appeared along with the abuse of antibiotics. Especially, wound in diabetic patients provides more glucose for bacteria resulting in poor wound healing. Therefore, it is imminent to explore advanced agents for combating multidrug-resistant bacteria and accelerating diabetic wound healing. Herein, metal-organic frameworks based nanoreactors loaded with glucose oxidase (GOx) and peroxidase-like bovine hemoglobin (BHb) are designed to construct an effective cascaded catalytic antibacterial system. Therein, GOx can cost the glucose, and release H2O2 simultaneously, which can then be transformed into hydroxyl radicals by BHb. As a result, the as-prepared nanoreactors can play the roles of both starving and killing toward the multidrug-resistant bacteria. Furthermore, the produced gluconic acid can reduce the pH of working condition, which is beneficial for both the enhancement of peroxidase activity and the inhibition of the bacteria growth. More importantly, the constructed nanoreactors can be degraded and excreted from the body in the form of feces, which render the as-proposed nanoreactors qualified as effective and safe materials for both combating multidrug-resistant bacteria in vitro and accelerating the diabetic wound healing in vivo of the mouse model.
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