ACS Applied Materials & Interfaces · 2024 · 13 citations · 54 references
EngineeringBioengineeringBiotechnologyBiosensorsElectroanalytical MethodsEnzymologyElectrochemical BiosensorsElectrochemical DetectionElectrochemical SensorsEnzymatic BiosensorsNanomaterial-based BiosensorsSignal Amplification StrategiesCascade ReactionsDifferential Pulse VoltammetryEnzyme ActivityEnzyme-based NanobiosensorsNanoparticle-based ProbesSignal ReadoutSquare-wave VoltammetryVoltammetry
Balancing the accuracy and simplicity of aptasensors is a challenge in their construction. This study addresses this issue by leveraging the remarkable loading capacity and peroxidase-like catalytic activity of PtPdCu trimetallic nanoparticles, which reduces the reliance on precious metals. A dual-signal readout aptasensor for enrofloxacin (ENR) detection is designed, incorporating DNA dynamic network cascade reactions to further amplify the output signal. Exploiting the strong loading capacity of PtPdCu nanoparticles, they are self-assembled with thionine (Thi) to form a signal label capable of generating signals in two independent modes. The label exhibits excellent enzyme-like catalytic activity and enhances electron transfer capabilities. Differential pulse voltammetry (DPV) and square-wave voltammetry (SWV) are employed to independently read signals from the oxidation–reduction reaction of Thi and the catalytic oxidation of hydroquinone (HQ) to benzoquinone (BQ) by H 2 O 2 . The introduced DNA dynamic network cascade reaction modularizes sample processing and electrode surface signal generation, avoiding electrode contamination and efficiently increasing the output of the catalyzed hairpin assembly (CHA) cycle. Under optimized conditions, the developed aptasensor demonstrates detection limits of 0.112 (DPV mode) and 0.0203 pg/mL (SWV mode). Additionally, the sensor successfully detected enrofloxacin in real samples, expanding avenues for designing dual-mode signal amplification strategies.
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