In situ enhanced electrochemiluminescence based on co-reactant self-generated for sensitive detection of microRNA

An ultrasensitive and selective miRNA biosensor based on the luminol-H 2 O 2 electrochemiluminescence (ECL) system using hemin as a catalyzer for in situ ECL signal enhancement was reported. DNA probe was tethered onto the electrodeposited Au nanoparticles on a glassy carbon electrode, and the remaining active sites were then blocked with glucose oxidase (GOD). Subsequently, followed by miRNA hybridizing with the DNA probe, hemin molecules acted as the essential enhancer of ECL were intercalated into the DNA/miRNA duplex structure. The fully constructed biosensor was placed in a phosphate buffered solution containing luminol and glucose, where glucose was enzymatically decomposed by GOD to H 2 O 2 . Formation of reactive oxygen species (O 2 − ) from H 2 O 2 , which was a key step for luminol ECL production, was efficiently catalyzed by the intercalated hemin. Thus, enhanced ECL signal was obtained. Under the optimal conditions, this miRNA biosensor could sensitively and selectively detect target miRNA over approximately seven orders of magnitude between 0.050 and 1.0   ×   10 5   pM, with a limit of detection of 50   fM. miRNAs extracted from the A459 cell line were quantified with the biosensor. The ECL enhancement strategy presented in this paper could open a new route for the development of extremely sensitive ECL based biosensors.