4.8 Article

pH-Responsive Oxygen and Hydrogen Peroxide Self-Supplying Nanosystem for Photodynamic and Chemodynamic Therapy of Wound Infection

期刊

ACS APPLIED MATERIALS & INTERFACES
卷 13, 期 50, 页码 59720-59730

出版社

AMER CHEMICAL SOC
DOI: 10.1021/acsami.1c19681

关键词

photodynamic therapy (PDT); chemodynamic therapy (CDT); metal-organic frameworks (MOFs); antibacterial therapy; graphene quantum dots

资金

  1. National Science Foundation of China [61901405]
  2. Natural Science Foundation of Jiangsu Province, China [BK20201156]
  3. Xuzhou Natural Science Foundation, China [KC18108, KC19066]
  4. Excellent Talents Scientific Research Project [D2019026]
  5. China Postdoctoral Science Foundation [2020M671608]
  6. Jiangsu Graduate Scientific Research Innovation Project [KYCX21_2727]

向作者/读者索取更多资源

The study designed a pH-responsive nanosystem that combines photodynamic therapy and chemodynamic therapy for wound infection. The system showed a combined PDT/CDT effect, killing bacteria through oxidative stress and enhancing therapeutic effects by activating the immune response.
The combination of photodynamic therapy (PDT) and chemodynamic therapy (CDT) has been continuously explored in the antibacterial aspect and has achieved more effective antibacterial effect than a single therapy. We design a pH-responsive O-2 and H2O2 self-supplying zeolitic imidazolate framework-67 (ZIF-67) nanosystem for PDT/CDT of wound infection. Under the acidic inflammatory conditions, ZIF-67 can degrade to produce Co2+ and release CaO2 and graphene quantum dots (GQDs). The exposed CaO2 reacted with water to generate H2O2 and O-2. The self-supplied O-2 alleviates hypoxia at the site of inflammation and enhances external light-initiated GQD-mediated PDT, while H2O2 was catalyzed by endogenous Co2+ to produce hydroxyl radicals for Co2+-triggered CDT. In vitro and in vivo experiments confirm that CaO2/GQDs@ZIF-67 has a combined PDT/CDT effect. The antibacterial mechanism indicates that bacteria post-treated with CaO2/GQDs@ZIF-67 may be sterilized by reactive oxygen species-mediated oxidative stress and the leakage of bacterial contents. The experiments also find that CaO2/GQDs@ZIF-67 may activate the immune response and enhance the therapeutic effect by activating the cyclic GMP-AMP synthase-stimulator of interferon genes signaling pathway.

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