EngineeringBioengineeringChemical EngineeringBiosensorsElectroanalytical MethodsNanomaterialsElectrochemical BiosensorsInorganic NanoparticlesNanomaterial-based BiosensorsNanosensorsQuantum DotsQuantum Dots In BiologyAmplificationAssayBiomolecular DetectionDifferential Pulse VoltammetryLinear RangeRolling Circle AmplificationUltrasensitive DetectionVoltammetry
Cd-based semiconductor quantum dots (QDs) with size-tunable luminescence and high quantum yield have become the most promising electrochemiluminescence (ECL) emitters. However, their unavoidable biotoxicity limited their applications in bioassays. Here, the nontoxic and economical MoS 2 QDs prepared by chemical exfoliation from the bulk MoS 2 were first investigated as new ECL emitters, and then the possible luminescence mechanism of MoS 2 QDs was studied using ECL-potential curves and differential pulse voltammetry (DPV) methods in detail. With MoS 2 QDs as the ECL emitters and triethylamine (TEA) as the efficient coreactant, a practical and label-free aptasensor for lipopolysaccharide (LPS) detection was constructed based on aptamer recognition-driven target-cycling synchronized rolling circle amplification. Comparing to conventional stepwise reactions, this target-cycling synchronized rolling circle amplification achieved more efficient signal amplification and simpler operation. The developed assay for LPS detection demonstrated a wide linear range of 0.1 fg/mL to 50 ng/mL with limit of detection down to 0.07 fg/mL. It is worth mentioning that MoS 2 QDs with stable ECL emission exhibited a great application potential in ECL bioanalysis and imaging as a new type of excellent emitter candidates.
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