材料科学
静电纺丝
复合数
生物材料
纳米技术
模数
纳米尺度
脚手架
复合材料
聚合物
生物医学工程
医学
作者
Yusai Zhou,Jingjing Deng,Yi Zhang,Cong Li,Wei Zheng,Jianlei Shen,Jingjing Li,Fan Wang,Bing Han,Dong Chen,Chunhai Fan,Hongjie Zhang,Kai Liu,Yan Wei
标识
DOI:10.1002/adma.202202180
摘要
Programmable base pair interactions at the nanoscale make DNA an attractive scaffold for forming hydroxyapatite (HAP) nanostructures. However, engineering macroscale HAP mineralization guided by DNA molecules remains challenging. To overcome this issue, a facile strategy is developed for the fabrication of ultrastiff DNA-HAP bulk composites. The electrostatic complexation of DNA and a surfactant with a quaternary ammonium salt group enables the formation of long-range ordered scaffolds using electrospinning. The growth of 1D and 2D HAP minerals is thus realized by this DNA template at a macroscale. Remarkably, the as-prepared DNA-HAP composites exhibit an ultrahigh Young's modulus of ≈25 GPa, which is comparable to natural HAP and superior to most artificial mineralized composites. Furthermore, a new type of dental inlay with outstanding antibacterial properties is developed using the stiff DNA-HAP. The encapsulated quaternary ammonium group within the dense HAP endows the composite with long-lasting and local antibacterial activity. Therefore, this new type of super-stiff biomaterial holds great potential for oral prosthetic applications.
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