A ratiometric fluorescence strategy based on inner filter effect for Cu2+-mediated detection of acetylcholinesterase

Abstract

A novel ratiometric fluorescence strategy for 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 598 nm and quenched the fluorescence of g-CNQD at 438 nm. 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 598 nm and recovered that of g-CNQD at 438 nm. In the presence of AChE it catalyzed the hydrolysis of acetylthiocholine (ATCh) to produce thiocholine (TCh) which competed with ARS for binding to Cu²⁺; thus, the fluorescence at 598 nm increased and that at 438 nm 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 0.5-15 mU/mL with a detection limit of 0.36 mU/mL. The method was successfully applied to the determination of AChE in human serum and the screening of inhibitors.

Keywords: Acetylcholinesterase; Alizarin red S; Carbon nitride quantum dots; Copper ion; Phenylboronic acid; Ratiometric fluorescence strategy.