化学
冠醚
离子
选择性
体内
纳米技术
无机化学
有机化学
材料科学
催化作用
生物技术
生物
作者
Jiahao Liu,Jiahao Lu,Wenliang Ji,LU Guang-wen,Jiao Wang,Tingyan Ye,Yisha Jiang,Juanjuan Zheng,Ping Yu,Nannan Liu,Yanan Jiang,Lanqun Mao
标识
DOI:10.1021/acs.analchem.3c05366
摘要
In vivo sensing of the dynamics of ions with high selectivity is essential for gaining molecular insights into numerous physiological and pathological processes. In this work, we report an ion-selective micropipette sensor (ISMS) through the integration of functional crown ether-encapsulated metal–organic frameworks (MOFs) synthesized in situ within the micropipette tip. The ISMS features distinctive sodium ion (Na+) conduction and high selectivity toward Na+ sensing. The selectivity is attributed to the synergistic effects of subnanoconfined space and the specific coordination of 18-crown-6 toward potassium ions (K+), which largely increase the steric hindrance and transport resistance for K+ to pass through the ISMS. Furthermore, the ISMS exhibits high stability and sensitivity, facilitating real-time monitoring of Na+ dynamics in the living rat brain during spreading of the depression events process. In light of the diversity of crown ethers and MOFs, we believe this study paves the way for a nanofluidic platform for in vivo sensing and neuromorphic electrochemical sensing.
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