Photo-assisted biofuel cell-based
self-powered biosensors (PBFC-SPBs)
possess the advantages of no need for external power supply, ease
of sensing design, and simple instruments. In this work, a robust
anti-interference PBFC-SPB for microRNA detection was constructed
based on the Pt–S bond and the inorganic–organic hybridization
strategy. The organic semiconductor [6,6]-phenyl-C61-butyric acid
methylester@anthraquinone (PCBM@anthraquinone) served as an efficient
light-harvesting material, and gold nanoparticle@Pt (AuNP@Pt) nanomaterials
were immobilized on the surface via electrostatic adsorption for the
binding of DNA. Notably, compared to Au–S bonds for DNA immobilization,
the Pt–S bond exhibited better anti-interference ability. Ingeniously,
cadmium sulfide quantum dots (CdS QDs) were close to the PCBM@anthraquinone
substrate electrode to form sensitization structures, which was beneficial
to enhance the photocurrent signal. Combining with the laccase-mimicking
activity Cu2+/carbon nanotubes (Cu2+/CNTs) cathode,
the PBFC-SPB for microRNA detection was achieved. Once the target
existed, the identical sequence complementary microRNA would make
DNA2/CdS dissociate and break away from the electrode, leading to
a low signal. The linear detection range was 10 fM–100 pM,
with the limit of determination of 2.4 fM (3S/N). The as-proposed strategy not only paves a new way for
the design of photoelectrochemical biosensing but also opens a door
for the construction of robust anti-interference bioassay for microRNA
detection.