Ion-Selective Micropipette Sensor for In Vivo Monitoring of Sodium Ion with Crown Ether-Encapsulated Metal-Organic Framework Subnanopores

被引:5
|
作者
Liu, Jiahao [1 ,2 ]
Lu, Jiahao [2 ,3 ]
Ji, Wenliang [2 ]
Lu, Guangwen [2 ]
Wang, Jiao [2 ]
Ye, Tingyan [1 ]
Jiang, Yisha [1 ]
Zheng, Juanjuan [1 ]
Yu, Ping [3 ,4 ]
Liu, Nannan [1 ]
Jiang, Yanan [2 ]
Mao, Lanqun [2 ]
机构
[1] Wenzhou Univ, Coll Chem & Mat Engn, Key Lab Carbon Mat Zhejiang Prov, Wenzhou 325027, Peoples R China
[2] Beijing Normal Univ, Coll Chem, Beijing 100875, Peoples R China
[3] Chinese Acad Sci, Inst Chem, Beijing Natl Lab Mol Sci, Key Lab Analyt Chem Living Biosyst, Beijing 100190, Peoples R China
[4] Univ Chinese Acad Sci, Beijing 100049, Peoples R China
基金
中国国家自然科学基金;
关键词
CRYSTAL-STRUCTURE; CHANNELS; REVEALS; BRAIN;
D O I
10.1021/acs.analchem.3c05366
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
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.
引用
收藏
页码:2651 / 2657
页数:7
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