A Universal Metal–Flavonoid Coating Strategy: Engineering Biomaterials for Diabetic Bone Regeneration

Under metabolic disorders such as diabetes, the regenerative capacity of bone tissue is compromised, characterized by hyperglycemia-induced oxidative stress, impaired osteogenesis, and dysregulated angiogenesis. These complications undermine the efficacy of conventional bone repair materials, limiting their capacity to promote effective healing. Herein, we developed a metal-flavonoid functionalized coating strategy that integrates osteogenic and angiogenic metal ions with natural antioxidant flavonoids. Leveraging their chelation ability and strong surface affinity, a one-pot approach is established to endow conventional bone repair materials with tailored biofunctions that modulate the diabetic bone microenvironment and facilitate regeneration. Among the tested candidates, copper-quercetin (CQ) coating is screened as the optimal formulation owing to its potent antioxidative, osteoinductive, and pro-angiogenic properties under high-glucose (HG) conditions. Conventional bone repair materials (e.g., β-tricalcium phosphate, β-TCP) modified with this coating significantly ameliorated oxidative stress, restored osteogenesis, and rescued angiogenesis impaired by persistent hyperglycemia. In diabetic rats, CQ-coated β-TCP (β-TCP@CQ) accelerated bone healing by 1.68-fold compared to unmodified controls. Mechanistically, the CQ coating activated the ATP7A/SOD3/FLT1 axis to restore copper homeostasis in bone marrow mesenchymal stem cells while stimulating the PI3K-Akt pathway to enhance osteogenic differentiation. Moreover, the coating exhibited broad versatility across multiple biomaterial compositions (metals, ceramics, polymers, and composites) and structures (2D discs, 3D scaffolds). This metal-flavonoid coating strategy demonstrated feasibility and scalability, while also providing a mechanistic foundation and technical platform for the effective use of conventional bone repair materials in complex pathological contexts.

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Publication Details

Journal
Advanced Science
Published
2026-01-08
DOI
https://doi.org/10.1002/advs.202522509
Citations
2
Primary Topic
Bone Tissue Engineering Materials
Type
article
Field-Weighted Citation Impact
42.56
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article

A Universal Metal–Flavonoid Coating Strategy: Engineering Biomaterials for Diabetic Bone Regeneration

C Q Dong, Lefeng Su, Qishu Jin, Chunlong Zhang et al.
2 citations
Advanced Science
Bone Tissue Engineering Materials
42.56
article

A Universal Metal–Flavonoid Coating Strategy: Engineering Biomaterials for Diabetic Bone Regeneration

C Q Dong, Lefeng Su, Qishu Jin, Chunlong Zhang, Zhaowenbin Zhang, Jiandong Yuan, Yihao Wu, Lingyi Hu, Jiang Chang, Chen Yang, Zhiqiang Liu, Hao Chen
article en
2 citations

Abstract

Under metabolic disorders such as diabetes, the regenerative capacity of bone tissue is compromised, characterized by hyperglycemia-induced oxidative stress, impaired osteogenesis, and dysregulated angiogenesis. These complications undermine the efficacy of conventional bone repair materials, limiting their capacity to promote effective healing. Herein, we developed a metal-flavonoid functionalized coating strategy that integrates osteogenic and angiogenic metal ions with natural antioxidant flavonoids. Leveraging their chelation ability and strong surface affinity, a one-pot approach is established to endow conventional bone repair materials with tailored biofunctions that modulate the diabetic bone microenvironment and facilitate regeneration. Among the tested candidates, copper-quercetin (CQ) coating is screened as the optimal formulation owing to its potent antioxidative, osteoinductive, and pro-angiogenic properties under high-glucose (HG) conditions. Conventional bone repair materials (e.g., β-tricalcium phosphate, β-TCP) modified with this coating significantly ameliorated oxidative stress, restored osteogenesis, and rescued angiogenesis impaired by persistent hyperglycemia. In diabetic rats, CQ-coated β-TCP (β-TCP@CQ) accelerated bone healing by 1.68-fold compared to unmodified controls. Mechanistically, the CQ coating activated the ATP7A/SOD3/FLT1 axis to restore copper homeostasis in bone marrow mesenchymal stem cells while stimulating the PI3K-Akt pathway to enhance osteogenic differentiation. Moreover, the coating exhibited broad versatility across multiple biomaterial compositions (metals, ceramics, polymers, and composites) and structures (2D discs, 3D scaffolds). This metal-flavonoid coating strategy demonstrated feasibility and scalability, while also providing a mechanistic foundation and technical platform for the effective use of conventional bone repair materials in complex pathological contexts.

Advanced ScienceVol. 13(10)
Wenzhou University (CN), Donghua University (CN), Wenzhou Medical University (CN), First Affiliated Hospital of Wenzhou Medical University (CN), Soochow University (CN), First Affiliated Hospital of Soochow University (CN), Huazhong University of Science and Technology (CN), Yangzhou University (CN)
Openalex Percentile: Top 0%
Bone Tissue Engineering Materials
42.56
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