Conjugated Polymer-Boosted Near-infrared Electrochemiluminescence of Organic Dye for Detecting Acetamiprid

Abstract

Background

The near-infrared electrochemiluminescence (NIR-ECL) has excellent penetration and near zero background interference, and has shown unique advantages in clinical medicine and bioimaging. Among various types of NIR-ECL emitters, NIR organic dyes have arouse the concern of researchers due to their adjustable structure and diverse optical properties. However, the currently available NIR dyes usually have inherent self-quenching effect and poor photostability, so their ECL efficiency is low, and it is a great challenge to improve their ECL performance.

Result

Conjugated polymer-boosted NIR-ECL strategy was creatively developed to overcome ECL performance limitations of NIR dyes. IR 783, as one of heptamethine cyanine dyes, was performed a nanoprecipitation in the presence of poly[(9,9-dlhexyfluoren-2,7-dlyl)-co-(anthracen-9,10-dlyl)] (PFAD) to prepare IR polymer nanoparticles (IR PNPs). Due to resonance energy transfer (RET) from PFAD to IR 783 and encapsulation of IR 783 by PFAD, the resulting IR PNPs exhibited a strong and stable NIR-ECL emission with a maximum ECL wavelength of 802 nm under coreactant tripropylamine (TPrA) and H₂O₂ can effectively quench it. IR PNPs coupled proximity ligation assay (PLA)-induced DNA walker to achieve acetamiprid (ACE) analysis. ACE triggered PLA to form bipedal DNA walker, and further release G-rich secondary target (ST). With ST and hemin being captured on IR PNPs modified electrode, hemin/G-quadruplex was assembled to consume H₂O₂, thereby restoring ECL signal for ACE detection with a limit of detection of 4.74 ×10^-15 M.

Significance

This work opens up a new and simple way to boost NIR-ECL of organic dyes, and IR PNPs create a promising NIR-ECL platform for pesticide detection.