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水凝胶支架修复骨质疏松骨缺损的机制及研究进展

黄筱涵 刘钰林 李秀茹 陆真慧 江献芳 郑立

中国比较医学杂志2026,Vol.36Issue(15):118-127,10.
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中国比较医学杂志2026,Vol.36Issue(15):118-127,10.DOI:10.3969/j.issn.1671-7856.2026.15.012

水凝胶支架修复骨质疏松骨缺损的机制及研究进展

The mechanisms and advances in hydrogel scaffold repair of osteoporotic bone defects

黄筱涵 1刘钰林 2李秀茹 2陆真慧 2江献芳 1郑立2

作者信息

  • 1. 广西口腔颌面修复与重建研究重点实验室,广西颅颌面畸形临床医学研究中心,广西医科大学口腔医学院/附属口腔医院,南宁 530021
  • 2. 广西医科大学第一附属医院,广西再生医学重点实验室,广西组织器官再生生物医学材料工程中心,再生医学与医用生物资源开发与应用协同创新中心,南宁 530021
  • 折叠

摘要

Abstract

Osteoporosis(OP)is a systemic metabolic disease characterized by disrupted bone homeostasis.Bone defects caused by OP are difficult to repair owing to an imbalanced bone microenvironment.Traditional therapies have limited efficacy,numerous complications,and complex treatment procedures.Hydrogel scaffolds have emerged as novel repair materials owing to their excellent biocompatibility and unique network structure,which can repair osteoporotic bone defects by promoting angiogenesis and regulating immune responses.This review systematically summarizes the development status and therapeutic mechanisms of hydrogel scaffolds in repairing osteoporotic bone defects,and discusses their application prospects and limitations.Multi-material hydrogel systems can facilitate the osteoporotic bone defect repair through intelligent environmental responses and diverse bioactive molecules or cell delivery,representing an ideal therapeutic strategy.Future research may focus on advancing the functional modification and clinical translation of hydrogels,and provide new directions and insights for basic research and clinical treatment of osteoporotic bone defects through in-depth investigations into their mechanisms of action.

关键词

骨质疏松/骨缺损/水凝胶/组织工程/骨修复/生物材料

Key words

osteoporosis/bone defect/hydrogel/tissue engineering/bone repair/biological material

分类

医药卫生

引用本文复制引用

黄筱涵,刘钰林,李秀茹,陆真慧,江献芳,郑立..水凝胶支架修复骨质疏松骨缺损的机制及研究进展[J].中国比较医学杂志,2026,36(15):118-127,10.

基金项目

国家自然科学基金(52573316,82160188) (52573316,82160188)

广西医科大学一流学科创新驱动人才计划(江献芳). (江献芳)

中国比较医学杂志

1671-7856

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