化学
荧光团
部分
荧光
纳米技术
金属有机骨架
纳米尺度
分析物
生物分子
材料科学
有机化学
吸附
光学
生物化学
物理
物理化学
作者
Chan Yang,Kun Chen,Mei Chen,Xiaoxiao Hu,Shuangyan Huan,Lanlan Chen,Guosheng Song,Xiaobing Zhang
标识
DOI:10.1021/acs.analchem.8b04405
摘要
Nanoscale metal–organic frameworks (NMOFs) have been applied for biomedical sensing in recent years. However, it is still a great challenge to construct a highly efficient NMOFs fluorescent probe for sensing in a biological system, with high signal-to-noise ratio, photostability, and deep tissue penetration. Herein, for the first time, we report the two-photon metal–organic framework (TP-MOF) as a sensing platform. The design of TP-MOF is based on NMOFs incorporating a target-responsive two-photon organic moiety through click chemistry. PCN-58, as a model building block, was covalently modified with a small-molecule probe for H2S or Zn2+ as model analytes. TP-MOF probes retain the fluorescence-responsive properties of the TP organic moiety and possess excellent photostability and selectivity, as well as biocompatibility. Benefiting from the near-infrared (∼820 nm) excited two-photon fluorophore, TP-MOF probes serve to sense and image their respective targets in live cells and tissue slices with a penetration of 130 μm. The molecular design presented here bodes well for the extension to other MOFs displaying sensing components for other analytes of interest.
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