4.8 Article

Photothermal Nanozyme-Based Microneedle Patch against Refractory Bacterial Biofilm Infection via Iron-Actuated Janus Ion Therapy

期刊

ADVANCED MATERIALS
卷 34, 期 51, 页码 -

出版社

WILEY-V C H VERLAG GMBH
DOI: 10.1002/adma.202207961

关键词

bacterial biofilm infections; ferroptosis; immune regulation; ion therapy; nanozyme-based microneedle patches

资金

  1. National Natural Science Foundation of China [81802181, 81871788, 82202672]
  2. Key Research and Development Program of Anhui Province [202004j07020013, 201904a07020097, 2022e07020017]
  3. Natural Science Foundation of Anhui Province [2108085QH319]
  4. Fundamental Research Funds for the Central Universities [WK9110000152, WK9110000173]
  5. Excellent Youth Training Program of Shanghai Jiao Tong University Affiliated Shanghai Sixth People's Hospital [ynyq202202]

向作者/读者索取更多资源

The study proposed a novel antibiofilm strategy to eliminate bacterial biofilm infections by regulating iron metabolism in both bacterial biofilm and immune cells. The experimental results showed that more than 95% of BBIs elimination can be achieved by combining heat stress-triggered iron interference with iron-nutrient immune reactivation.
Owing to high antibiotic resistance and thermotolerance, bacterial biofilm infections (BBIs) are refractory to elimination. Iron is essential for bacterial growth and metabolism, and bacteria can thus accumulate iron from surrounding cells to maintain biofilm formation and survival. Consequently, iron deficiency in the biofilm microenvironment (BME) leads to the functional failure of innate immune cells. Herein, a novel antibiofilm strategy of iron-actuated Janus ion therapy (IJIT) is proposed to regulate iron metabolism in both bacterial biofilm and immune cells. A BME-responsive photothermal microneedle patch (FGO@MN) is synthesized by the growth of Fe3O4 nanoparticles on graphene oxide nanosheets and then encapsulated in methacrylated hyaluronic acid needle tips. The catalytic product of center dot OH by FGO@MN in BME disrupts the bacterial heat-shock proteins, coercing biofilm thermal sensitization. As synergistic mild photothermal treatment triggers iron uptake, the intracellular iron overload further induces ferroptosis-like death. Moreover, iron-nourished neutrophils around BME can be rejuvenated for reactivating the suppressed antibiofilm function. Thus, more than 95% BBIs elimination can be achieved by combining heat stress-triggered iron interference with iron-nutrient immune reactivation. Furthermore, in vivo experiments validate the scavenging of refractory BBI after 15 days, suggesting the promising perspective of IJIT in future clinical application.

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