材料科学
纳米尺度
罗丹明6G
分子
纳米技术
生物相容性
适体
药物输送
微流控
DNA
罗丹明B
化学工程
生物物理学
组合化学
有机化学
化学
生物
遗传学
光催化
工程类
生物化学
催化作用
冶金
作者
Xiyue Cao,Jianfei Xia,Xuan Meng,Jiaoyan Xu,Qingyun Liu,Zonghua Wang
标识
DOI:10.1002/adfm.201902237
摘要
Abstract Stimuli‐responsive nanoscale porous carbon derived from ZIF‐8 (NCZIF) gated by DNA capping units is reported. The NCZIF is first obtained by calcination of nano‐ZIF‐8 crystals under an inert atmosphere. It is further conjugated with amine‐modified single‐stranded DNA after carboxylation (DNA/NCZIF). The guest molecules are sealed in the pore of NCZIF by the formation of a DNA duplex structure on the surface of NCZIF. As proof of principle, two systems that can be, respectively, used for controlled drug delivery and biosensing are introduced. In the first system, the drug model (rhodamine 6G, Rh6G) is locked in the NCZIF by the DNA capping units composed of rich‐G sequences and its complementary DNA strand. The in vitro cellular experiments reveal that DNA/NCZIF has good biocompatibility and can controllably release Rh6G upon the K + ‐stimuli in cells. In the second system, the signal probe (methylene blue, MB) is locked in the NCZIF and then released after the unlocking of the pores triggered by the dissociation of the aptamer‐hybrid capping units. The MB‐loaded DNA/NCZIF can linearly respond to target molecules in the range from 1 × 10 −9 to 10 × 10 −6 m and has good specificity.
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