Naringenin-Loaded Core-Shell Mg-MOF Nanocomposite Integrated Injectable Hydrogel for Bone Regeneration: Anti-inflammatory, Osteogenic, and Angiogenic

  • Biomacromolecules. 2025 Oct 17. doi: 10.1021/acs.biomac.5c01230.
Chaonan He  1 Peipei Feng  1 Dingli Xu  2 Leidong Lian  2 Jin Li  1 Kaifeng Gan  1 Yi Gu  1 Tingting Pan  1 Yun Tang  1 Xiang Wu  1 Zhaoxiang Peng  1 Chunhai Ke  1 Jingyun Ma  1
Affiliations
  • 1. The Affiliated Lihuili Hospital of Ningbo University, Ningbo, Zhejiang 315040, PR China.
  • 2. Health Science Center, Ningbo University, Ningbo, Zhejiang 315040, PR China.
Abstract

Composite biomaterial systems facilitate regenerative medicine through component synergy. Herein, novel core-shell nanocomposites (N-HMMs) are prepared, with hollow mesoporous silica (HMSNs) as the core and magnesium-gallic acid metal-organic frameworks (Mg-MOFs) as the shell. N-HMMs are loaded with the small-molecule osteoinductive drug naringin (Nar) to form N-HMMs@Nar, which is integrated into methacrylate gelatin/polyethylene glycol diacrylate hydrogels (GelMA/PEGDA, GP) to construct N-HMMs@Nar@GP. N-HMMs@Nar@GP enables sustained release of Nar, bioactive Mg2+, and antioxidant gallic acid for synergistic anti-inflammation, osteogenesis, and angiogenesis of bone regeneration. GP adapts N-HMMs@Nar to the traumatic characteristics of bone defects and facilitates in situ treatments. In vitro studies have confirmed the composite materials' biocompatibility, osteoinductive differentiation, and angiogenesis capabilities. The ability of N-HMMs@Nar@GP to enhance osteogenesis and angiogenesis is demonstrated in an in vivo tibial defect model using micro-CT and histopathological analysis. Therefore, N-HMMs@Nar@GP holds significant potential for application in the repair of bone defects.

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