材料科学
生物矿化
再生(生物学)
钙
骨愈合
控制释放
自愈水凝胶
生物医学工程
组织工程
化学工程
纳米技术
透明质酸
生物相容性材料
仿生学
磷酸盐
生物物理学
矿化组织
人造骨
骨组织
体内
磷灰石
仿生合成
化学
作者
Mingming Zhao,Yan Yu,Wenlong Zhang,Xiaonong Zhang,Chunsheng Xiao,Xuesi Chen
标识
DOI:10.1002/adfm.202517906
摘要
Abstract Through biomimicry of natural biomineralization processes, biomimetic mineralized hydrogels have demonstrated exceptional osteoconductive and osteoinductive properties. However, given the stage‐specific nature of bone repair, developing hydrogels capable of sequential multifactor release to match the evolving biological requirements in bone regeneration remains a significant challenge. Here, a magnesium calcium phosphate mineralized hydrogel (MCPMH) is reported with sequential multifactor release behavior. The MCPMH is facilely prepared by directly mixing sodium hyaluronate (HA), alendronate sodium (ADA), Ca 2+ , and Mg 2+ in deionized water. It undergoes spontaneous mineralization, transitioning from a soft (≈2 kPa) to a stiff (≈92 kPa) hydrogel. Mechanistic studies reveal that ADA and Ca 2+ are stably entrapped within calcium phosphate (CaP) crystals, while Mg 2+ forms a loosely bound complex with ADA. This structure enables an on‐demand sequential release profile, i.e., quick early‐stage Mg 2+ release to promote angiogenesis, followed by sustained release of Ca 2+ and ADA for osteogenesis and remodeling. Moreover, in vivo evaluation in a rat critical‐sized calvarial defect model confirmed MCPMH's superior bone regeneration capacity. Overall, this work delineates a holistic strategy for fabricating biomimetic mineralized hydrogels with sequential multifactor release capabilities, underscoring their substantial promise as artificial bone repair materials in clinical settings.
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