An integrated and portable optoelectronic biosensing system for rapid post-extraction on-site quantification of Heterosigma akashiwo.

Rapid, species-level identification of harmful algal blooms (HAB) remains constrained by laboratory-based molecular workflows and bulky fluorescence instrumentation. We report an integrated portable optoelectronic biosensing system for post-extraction quantification of Heterosigma akashiwo 18S rDNA. The key innovation is not the GO-based recognition chemistry itself, but the analytical signal-reading and conversion strategy: GO-regulated fluorescence recovery is captured by a sealed lens-filter-PIN photodiode module and converted through a resistor-based current-to-voltage circuit into an amplified photovoltage output. FITC-labelled ssDNA probes are quenched by GO nanosheets and recover fluorescence upon target hybridization. The recovered fluorescence is excited by a fixed-wavelength 488 nm laser, filtered at 520 ± 10 nm, collected by a sealed optical detection head, converted from photocurrent to photovoltage across a 10 kΩ sense resistor, amplified 500-fold, and digitized for quantitative readout. This voltage-mode architecture eliminates reliance on benchtop fluorimeters, microscope-camera assemblies, or picoampere-level current instrumentation, thereby improving the portability and practical usability of GO-based fluorescence assays. Using a 12-well double-layer microfluidic cartridge and a modified Stern-Volmer linearization strategy, the system quantified target DNA over 10