ScholarWorks@성균관대학교

초록

To address the challenge of electroactive interferences derived from complex food matrices during homogeneous photoelectrochemical (PEC) biosensing, a "separated-coupling" electrolysis platform was rationally engineered for the ultrasensitive detection of ochratoxin A (OTA). Based on the analysis of the conduction band of the α-Fe2O3 photoanode and the H2O2 reduction potential, a matched energy-level gradient was established, providing an efficient driving force for directional electron flux toward the recognition electrode. Meanwhile, Pt(II) tetrakis(4-carboxyphenyl) porphyrin complex two-dimensional metal-organic framework (TCPP-Pt(II) 2D MOF) conferred the recognition electrode with an exceptional electrocatalytic capability toward H2O2 reduction. This configuration enabled a self-powered detection system with signal acquisition under reductive potential, effectively eliminated disturbances from co-existing electroactive species. Furthermore, an enzyme-free strategy based on DNA catalytic hairpin assembly (CHA) was utilized to establish a G-quadruplex/hemin cascade. This process achieved an efficient homogeneous recognition via a self-calibrated sensing protocol, where the target-induced CHA simultaneously consumes the substrates of methylene blue (MB) and H2O2 substrates. Such a dual-substrate regulatory mechanism delivers a controllable signal response, thus ensuring high precision and anti-interference stability. The platform achieved a broad linear range from 0.001 ng/mL to 200 ng/mL with a limit of detection (LOD) as low as 0.92 pg/mL, offering a robust solution for monitoring trace OTA in complex real samples.

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