Biosensors based on organic electrochemical transistors (OECTs) have been a research highlight in recent years owing to their remarkable biocompatibility, low operating voltage, and substantial signal amplification capability. Especially, as an emerging fundamental device for biosensing, OECTs show great potential for pH, ions, molecules, and biomarker sensing. This review highlights the research progress of biomolecule sensors based on OECTs, focusing on recent publications in the past 5 years. Specifically, OECT-based biomolecule sensors for small molecules (glucose, dopamine, lactate, etc. that act as signals or effectors), and macromolecules (DNA, RNA, proteins, etc. that are often used as markers in physiology and medicine), are summarized. Additionally, emerging technologies and materials used to enhance sensitivity, detection limits, and detection ranges are described comprehensively. Last, aspects of OECT-based biomolecule sensors that need further improvement are discussed along with future opportunities and challenges.

A super-hydrophilic pH-sensitive electrode with a porous TiO₂ thin film is proposed in this work and fabricated using the chemical etching method. In total, 30 groups of porous TiO₂ thin film were obtained by immersing a Ti sheet in NaOH, with the solution concentration ranging from 0.5–4 M and the reaction time ranging from 15–240 min. SEM, XRD, XPS, and a contact angle meter were used to investigate the influence of the chemical etching parameters on the morphology, composition, and wettability of the fabricated electrodes. The chemical etching parameters were found to have a significant influence on the specific surface area and the component of the films, which strongly affected the wettability and pH sensing characteristics of the electrodes. The electrode obtained with a solution concentration of 1 M and reaction time of 120 min is the ideal product because of its excellent wettability, with a contact angle of 5.46°, and good pH sensing characteristics in pH buffer solutions. The electrode also showed good stability regarding its wettability and pH sensing properties during storage and utilization.

We reported a highly efficient electrochemical immunosensor utilizing chitosan–graphene nanosheets (CS-GNs) nanocomposites for the detection of aflatoxin B₁ (AFB₁) in corn samples. The CS-GNs nanocomposites, serving as a modifying layer, provide a significant specific surface area and biocompatibility, thereby enhancing both the electron transfer rate and the efficiency of antibody immobilization. The electrochemical characterization was conducted utilizing both differential pulse voltammetry (DPV) and electrochemical impedance spectroscopy (EIS). Moreover, the antibody concentration, pH, antibody immobilization time, and immunoreaction time, were optimized. The results showed that the current change ($\Delta I$) before and after the immunoreaction demonstrated a strong linear relationship ($R^2=0.990$) with the AFB₁ concentration, as well as good specificity and stability. The linear range extended from 0.05 to 25 ng/mL, with a detection limit of 0.021 ng/mL ($S/N=3$). The immunosensor exhibited a recovery rate ranging from 97.3% to 101.4% in corn samples, showing a promising performance using an efficient method, and indicating a remarkable prospect for the detection of fungal toxins in grains.