单宁酸
磷酸八钙
壳聚糖
脚手架
海藻酸钠
化学
葛根素
葡萄糖醛酸
组织工程
化学工程
磷酸盐
钠
生物医学工程
生物化学
有机化学
医学
多糖
替代医学
病理
工程类
作者
Che Yan,Tengbin Shi,Lan Li,Robert Hong,Jun Lai,Ting‐Ting Huang,Renfeng Xu,Qi Zhao,Xiaolong Chen,Lei Dai,Yuan Zhou,Wenge Liu,Jinxin Lin
标识
DOI:10.1016/j.ijbiomac.2024.132632
摘要
Current limitations in mechanical performance and foreign body reactions (FBR) often lead to implant failure, restricting the application of bioceramic scaffolds. This study presents a novel 3D-printed scaffold that combines the release of anti-inflammatory drugs with osteogenic stimulation. Initially, the inorganic and organic phases were integrated to ensure the scaffold's mechanical integrity through catechol chemistry and the electrostatic interactions between tannic acid and quaternary ammonium chitosan. Subsequently, layers of polydopamine-encapsulated puerarin-loaded zeolitic imidazolate framework-8 (ZIF-8) were self-assembled onto the stent's surface, creating the drug-loaded scaffold that improved drug release without altering the scaffold's structure. Compared with unloaded scaffolds, the puerarin-loaded scaffold demonstrated excellent osteogenic differentiation properties along with superior anti-inflammatory and osteogenic effects in a range of in vitro and in vivo studies. RNA sequencing clarified the role of the TGF and NF/κB signaling pathways in these effects, further supporting the scaffold's osteogenic potential. This study introduces a novel approach for creating drug-loaded scaffolds, providing a unique method for treating cancellous bone defects.
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