化学
溶酶体
荧光
斑马鱼
细胞生物学
生物物理学
生物化学
基因
酶
物理
量子力学
生物
作者
Qinghua Hu,Cen Tang,Yuting Yin,Xiang‐he Kong,Chaowei Fu,Rong Hu,Hongqing Wang
标识
DOI:10.1021/acs.analchem.4c06695
摘要
The sensitive detection of the radioactive thorium (Th) ion with an oxidation state of +4 (Th4+) is of great significance for environmental protection and life safety. In this study, five fluorescence sensors with regulated donor-acceptor (D-A) interactions were constructed for Th4+ detection based on intramolecular charge transfer and aggregation-induced emission mechanisms. Among the developed sensors, TPE-D bearing electron-deficient π-bridge and weak D-A interactions presented ratiometric fluorescence detection behavior toward Th4+ in aqueous solution due to its aggregation-induced emission characteristics and unique D-A-D structures. Moreover, TPE-D showed excellent selectivity and sensitivity for Th4+ detection, and the detection limit was as low as 8.1 × 10-8 M. The sensing mechanism observation revealed that Th4+ could coordinate with the hydroxyl, imine, and carbonyl groups of TPE-D accompanied by an electron transfer process. In addition, TPE-D could selectively be enriched in the lysosome. Both the detection of Th4+ in the lysosome and liver of mice and zebrafish were realized based on this strategy, and a mobile-assisted detection approach toward Th4+ in actual water samples was also established with high sensitivity. This is the first report for Th4+ detection in organelles and organs, which provides a great significance and reliable strategy for radionuclide toxicology detection and analysis applications.
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