Abstract

A novel ratiometric fluorescence strategyfor detection of acetylcholestinerase (AChE) is proposed based on carbon nitride quantum dots (g-CNQD) and the complex (PA) formed between phenylboronic acid (PBA) and alizarin red S (ARS). PA showed fluorescence at 598nm and quenched the fluorescence of g-CNQD at 438nm. Through UV-visible absorption, fluorescence, and fluorescence lifetime measurements, the quenching effect was demonstrated as inner filter effect (IFE). When Cu2+ was added, the coordination of ARS and Cu2+ decreased the fluorescence of PA at 598nm and recovered that of g-CNQD at 438nm. In the presence of AChE itcatalyzed the hydrolysis of acetylthiocholine (ATCh) to produce thiocholine (TCh) which competed with ARS for binding to Cu2+; thus, the fluorescence at 598nm increased and that at 438nm decreased again. Under the mediation of Cu2+, the fluorescence ratio F598/F438 of PA-CNQD probe had good linear relationship with AChE concentration in the range 0.5-15mU/mL with a detection limit of 0.36mU/mL. The method was successfully applied to the determination of AChE in human serum and the screening of inhibitors.

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