Zif-8 Loading Gallic Acid For Promoting Bone Defect Repair

To address the challenges of the inadequate control of inflammatory responses and insufficient vascularization which affect the bone defect repair, we engineered a gallic acid (Ga)-integrated hybrid nanocomposite through the strategic incorporation of gold nanoparticles (Au NPs) within zeolitic imidazolate framework-8 (ZIF-8). The nanocomposite was structurally characterized by transmission electron microscopy (TEM), X-ray diffraction (XRD), and Fourier-transform infrared spectroscopy (FTIR). In-vitro evaluation of immunomodulation, vascularization, and osteogenesis were performed. The results demonstrated the material effectively suppressed inflammatory responses by inhibiting the NF-κB signaling pathway and downregulating pro-inflammatory mediators. It enhanced endothelial cell-mediated angiogenesis, facilitating early-stage vascularization in bone tissue. Furthermore, it intrinsically promoted osteogenic differentiation. The multifunctional drug delivery system provides a promising technique through spatiotemporal functional coordination to promoting bone defect repair.

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Publication Details

Journal
International Dental Journal
Published
2025-10-01
DOI
https://doi.org/10.1016/j.identj.2025.105677
Primary Topic
Bone Tissue Engineering Materials
Type
article
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article

Zif-8 Loading Gallic Acid For Promoting Bone Defect Repair

Xiaoyu Wang, Hongchen Sun, Xiaolin Yu
International Dental Journal
Bone Tissue Engineering Materials
article

Zif-8 Loading Gallic Acid For Promoting Bone Defect Repair

Xiaoyu Wang, Hongchen Sun, Xiaolin Yu
article en

Abstract

To address the challenges of the inadequate control of inflammatory responses and insufficient vascularization which affect the bone defect repair, we engineered a gallic acid (Ga)-integrated hybrid nanocomposite through the strategic incorporation of gold nanoparticles (Au NPs) within zeolitic imidazolate framework-8 (ZIF-8). The nanocomposite was structurally characterized by transmission electron microscopy (TEM), X-ray diffraction (XRD), and Fourier-transform infrared spectroscopy (FTIR). In-vitro evaluation of immunomodulation, vascularization, and osteogenesis were performed. The results demonstrated the material effectively suppressed inflammatory responses by inhibiting the NF-κB signaling pathway and downregulating pro-inflammatory mediators. It enhanced endothelial cell-mediated angiogenesis, facilitating early-stage vascularization in bone tissue. Furthermore, it intrinsically promoted osteogenic differentiation. The multifunctional drug delivery system provides a promising technique through spatiotemporal functional coordination to promoting bone defect repair.

International Dental JournalVol. 75
Sun Yat-sen University (CN), Stomatology Hospital (CN), Hospital of Stomatology, Sun Yat-sen University
Openalex Percentile: Top 68%
Bone Tissue Engineering Materials
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