纳米颗粒
脚手架
咪唑酯
化学工程
材料科学
锌
沸石咪唑盐骨架
原位
乳酸
化学
核化学
纳米技术
金属有机骨架
无机化学
有机化学
生物医学工程
冶金
细菌
医学
工程类
生物
遗传学
吸附
作者
Cijun Shuai,Jun Zan,Fang Deng,Youwen Yang,Shuping Peng,Zhenyu Zhao
标识
DOI:10.1021/acssuschemeng.0c08009
摘要
Zeolitic imidazolate framework-8 (ZIF-8) nanoparticles are able to act as effective reinforcements to enhance the overall performance of a poly-l-lactic acid (PLLA) scaffold due to its interface compatibility and natural degradability. Nevertheless, the fast degradation of ZIF-8 would release excessive zinc ions, which produces adverse effects on natural cell growth. In this study, a core–shell-structured nanoparticle, in which ZIF served as a core and hydroxyapatite (HA) served as a shell, was constructed by polydopamine (PDA)-induced in situ growth of HA on ZIF-8 nanoparticles, aiming to control the zinc ion release. Then, the core–shell-structured nanoparticle (ZIF-8@PDA-HA) was introduced into the PLLA scaffold using selective laser sintering. Results showed that the zinc ion concentration for the PLLA/ZIF-8@PDA-HA scaffold decreased by 65.3% after 28 days of immersion, as compared with the PLLA/ZIF-8 scaffold. Moreover, the in situ-synthesized HA possessed superior bioactivity, which effectively enhanced the mineralization ability of scaffolds and promoted cell adhesion, proliferation, and differentiation.
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