4.7 Article

Multifunctional MIL-101 nanoparticles with Fenton-like reactions to Co-deliver LL-37 peptide and Vancomycin for targeted NIR imaging and Drug-resistant bacteria treatment

期刊

CHEMICAL ENGINEERING JOURNAL
卷 435, 期 -, 页码 -

出版社

ELSEVIER SCIENCE SA
DOI: 10.1016/j.cej.2022.135084

关键词

Fenton-like reactions; Antimicrobial peptides; Synergistic therapy; Antibacterial resistance; NIR imaging

资金

  1. National Natural Science of China [82160659]
  2. Science and Technology Research Project of Jiangxi Education Department [GJJ190583, GJJ201103]
  3. PhD Start-up Fund of Science Research Project of Jiangxi Science and Technology Normal University [2020BSQD019]
  4. Open Project of Jiangxi Provincial Key Laboratory of Drug Design and Evaluation [JKLDE-KF-2003]
  5. Graduate Student Innovation Special Fund Project of Jiangxi Science and Technology Normal University [YC2021-X03]
  6. Undergraduate research project of Jiangxi Province [S202111318047]
  7. Undergraduate research project of Jiangxi Science and Technology Normal University [20211504104]

向作者/读者索取更多资源

Bacterial infections and antibiotic resistance have become a global healthcare crisis. In this study, a novel NIR imaging and synergistic antibacterial nano-system is reported for resistance bacterial infection therapy. The nano-system has the ability to monitor the progress of infection treatment and promote wound healing.
Bacterial infections and antibiotic resistance have become a global healthcare crisis. There is an urgent need to develop visualized therapeutic platforms that allow accurate imaging of the bacterial infections, successful eradication of bacteria and real-time monitoring of treatment progress. In this work, we report a novel NIR imaging and synergistic antibacterial nano-system (LL-37@MIL-101-Van) for resistance bacterial infection therapy. The multifunctional nano-system is fabricated by a MIL-101 core, which is covalently connected with Vancomycin and modified with targeted antimicrobial peptides LL-37 on the surface. The ability of monitoring the progress of infection treatment and effective promoting wound healing of bacterial infection are proved by in vivo MRSA-infected mice models. Under the environment of endogenous H2O2 overexpression and slightly acid bacterial infection, the excellent Fenton-like reaction activity of LL-37@MIL-101-Van could effectively catalyze the decomposition of H2O2 to produce hydroxyl radicals (center dot OH), which trigger highly efficient chemo-dynamic therapy (CDT) and tissue protection effect. By combining CDT with antibacterial peptides and antibiotics therapy, special targeting and synergistic killing of MRSA are successfully achieved in in vitro and in vivo antibacterial assays with excellent biocompatibility. Due to this, this study proposes a novel, high-efficient, multifunctional imaging and therapy system, which will open a new avenue for the design of synergistic antibacterial and diagnostic platforms in the future.

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