材料科学
自愈水凝胶
透明质酸
生物物理学
生物医学工程
脐静脉
纳米技术
体外
高分子化学
生物化学
化学
解剖
医学
生物
作者
Babatunde O. Okesola,Shilei Ni,Burak Derkuş,Carles C. Galeano,Abshar Hasan,Yuanhao Wu,Jopeth Ramis,Lee Buttery,Jonathan I. Dawson,Matteo D’Este,Richard O.C. Oreffo,David Eglin,Hongchen Sun,Álvaro Mata
标识
DOI:10.1002/adfm.201906205
摘要
Abstract Synthetic osteo‐promoting materials that are able to stimulate and accelerate bone formation without the addition of exogenous cells or growth factors represent a major opportunity for an aging world population. A co‐assembling system that integrates hyaluronic acid tyramine ( HA‐Tyr ), bioactive peptide amphiphiles ( GHK‐Cu 2+ ), and Laponite ( Lap ) to engineer hydrogels with physical, mechanical, and biomolecular signals that can be tuned to enhance bone regeneration is reported. The central design element of the multicomponent hydrogels is the integration of self‐assembly and enzyme‐mediated oxidative coupling to optimize structure and mechanical properties in combination with the incorporation of an osteo‐ and angio‐promoting segments to facilitate signaling. Spectroscopic techniques are used to confirm the interplay of orthogonal covalent and supramolecular interactions in multicomponent hydrogel formation. Furthermore, physico‐mechanical characterizations reveal that the multicomponent hydrogels exhibit improved compressive strength, stress relaxation profile, low swelling ratio, and retarded enzymatic degradation compared to the single component hydrogels. Applicability is validated in vitro using human mesenchymal stem cells and human umbilical vein endothelial cells, and in vivo using a rabbit maxillary sinus floor reconstruction model. Animals treated with the HA‐Tyr‐HA‐Tyr‐GHK‐Cu 2+ hydrogels exhibit significantly enhanced bone formation relative to controls including the commercially available Bio‐Oss.
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