Honeycomb-inspired ZIF-sealed interface enhances osseointegration via anti-infection and osteoimmunomodulation.

Biomaterials

Department of Orthopedics, Centre for Leading Medicine and Advanced Technologies of IHM, The First Affiliated Hospital of USTC, Division of Life Sciences and Medicine, University of Science and Technology of China, Hefei, Anhui, 230001, China. Electronic address:

Published: June 2024

AI Article Synopsis

  • Implant-associated infections (IAIs) are a major risk in orthopedic surgery because they interfere with bone healing and the immune system.
  • A novel drug delivery system, based on a zeolitic imidazolate framework (ZIF), was created to release glucose oxidase in an acidic infection environment, promoting disinfection.
  • The ZIF system not only prevents infections but also enhances bone repair by improving the immune environment and reducing inflammation, showcasing its potential for clinical use against IAIs.

Article Abstract

Implant-associated infections (IAIs) pose a significant threat to orthopedic surgeries. Bacteria colonizing the surface of implants disrupt bone formation-related cells and interfere with the osteoimmune system, resulting in an impaired immune microenvironment and osteogenesis disorders. Inspired by nature, a zeolitic imidazolate framework (ZIF)-sealed smart drug delivery system on Ti substrates (ZSTG) was developed for the "natural-artificial dual-enzyme intervention (NADEI)" strategy to address these challenges. The subtle sealing design of ZIF-8 on the TiO nanotubes ensured glucose oxidase (GOx) activity and prevented its premature leakage. In the acidic infection microenvironment, the degradation of ZIF-8 triggered the rapid release of GOx, which converted glucose into HO for disinfection. The Zn released from degraded ZIF-8, as a DNase mimic, can hydrolyze extracellular DNA, which further enhances HO-induced disinfection and prevents biofilm formation. Importantly, Zn-mediated M2 macrophage polarization significantly improved the impaired osteoimmune microenvironment, accelerating bone repair. Transcriptomics revealed that ZSTG effectively suppressed the inflammatory cascade induced by lipopolysaccharide while promoting cell proliferation, homeostasis maintenance, and bone repair. In vitro and in vivo results confirmed the superior anti-infective, osteoimmunomodulatory, and osteointegrative capacities of the ZSTG-mediated NADEI strategy. Overall, this smart bionic platform has significant potential for future clinical applications to treat IAIs.

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Source
http://dx.doi.org/10.1016/j.biomaterials.2024.122515DOI Listing

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