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May 17, 2026Materials0 citationsOpen Access

Vanadium-Doped Bioactive Glass-Modified GelMA/CMCS/HA Injectable Hydrogel for Osteosarcoma Postoperative Therapy and Bone Regeneration

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DJDazhong JinMHMiaomiao HeGYGuangfu Yin

Key Points

  • The aim is to develop an injectable hydrogel that aids in bone regeneration and minimizes tumor recurrence after osteosarcoma surgery.
  • Developed a GelMA/CMCS/HA hydrogel modified with vanadium-doped mesoporous bioactive glass (VMBG).
  • Conducted in vitro assessments to evaluate antitumor activity and osteogenic potential.
  • Monitored alkaline phosphatase activity and osteogenic marker expression for efficacy validation.
  • The hydrogel showed potent antitumor efficacy through V(V)/V(IV) valence cycling-driven reactive oxygen species generation.
  • Enhanced alkaline phosphatase activity and increased osteogenic marker expression were observed, indicating strong osteogenic potential.
  • Incorporation of CMCS improved healing at the defect site, while HA facilitated cell adhesion and growth.

Abstract

Surgical intervention is a primary treatment for osteosarcoma, often resulting in a tumorous bone defect with an irregular shape. Postoperative management is essential to minimize tumor recurrence risks and promote bone regeneration. To address these issues, we developed a multifunctional injectable, rapidly photo-curable hydrogel composed of gelatin methacryloyl/carboxymethyl chitosan/hyaluronic acid (GelMA/CMCS/HA), modified with vanadium-doped mesoporous bioactive glass (VMBG). The exceptional injectability enables seamless adaptation to irregular bone defects, offering a significant advantage over preformed implants, while the rapid photocurability of the hydrogel ensures stable fixation within minutes, thereby reducing potential risks during surgery. Furthermore, this platform exhibits dual therapeutic efficacy, characterized by antitumor activity and osteogenic induction. In vitro assessments demonstrated that V(V)/V(IV) valence cycling-driven ROS generation mediated its potent antitumor efficacy. Additionally, concurrent enhancement of alkaline phosphatase activity and osteogenic marker expression validated its osteogenic potential. The CMCS incorporation promoted healing at the defect site, while the HA addition created binding sites for cell adhesion and growth, thereby improving scaffold bioactivity. Collectively, this study presents the development and validation of a multifunctional GelMA/CMCS/HA hydrogel, highlighting its dual capability for bone regeneration and tumor suppression within tumor-associated bone microenvironments.

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Cite This Study

Jin et al. (2026) studied this question.

synapsesocial.com/papers/6a095bdd7880e6d24efe1c38https://doi.org/10.3390/ma19102086
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