生物相容性
聚己内酯
点击化学
化学
脚手架
树枝状大分子
生物降解
组织工程
生物界面
骨组织
生物医学工程
聚合物
材料科学
组合化学
生物化学
有机化学
纳米技术
医学
作者
Xifeng Liu,Areonna Schreiber,Maria Astudillo Potes,Babak Dashtdar,Abdelrahman M. Hamouda,Asghar Rezaei,Benjamin D. Elder,Lichun Lu
标识
DOI:10.1021/acs.biomac.4c00999
摘要
Traditional polymer systems often rely on toxic initiators or catalysts for cross-linking, posing significant safety risks. For bone tissue engineering, another issue is that the scaffolds often take a longer time to degrade, inconsistent with bone formation pace. Here, we developed an enzyme-responsive biodegradable poly(propylene fumarate) (PPF) and polycaprolactone (PCL) polyphosphoester (PPE) dendrimer cross-linked utilizing click chemistry (EnzDeg-click-PFCLPE scaffold) for enhanced biocompatibility and degradation. The strain-promoted alkyne–azide cycloaddition (SPAAC) offers high efficiency and biocompatibility without harmful agents. The polyphosphoesters render polymer cleavage responsive to alkaline phosphatase (ALP) enzyme in bone formation, ensuring facilitated scaffold biodegradation. The in vitro testing confirmed biocompatibility, enzyme-responsive degradation, and capability to support stem cell differentiation. Further in vivo implantation in rat demonstrated bone regeneration and scaffold integration. In summary, this polymer system combining click chemistry with ALP-responsive biodegradation ensures initial bone support and facilitates scaffold degradation synchronized with the natural bone healing process.
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