Alpha-fetoprotein (AFP) is widely-known as the most commonly used protein biomarker for liver cancer diagnosis at the early stage. Therefore, developing the highly sensitive and reliable method of AFP detection is of essential demand for practical applications. Herein, two types of aptamer-based AFP detection methods, i.e., optical and electrochemical biosensors, are reviewed in detail. The optical biosensors include Raman spectroscopy, dual-polarization interferometry, resonance light-scattering, fluorescence, and chemiluminescence. The electrochemical biosensors include cyclic voltammetry, electrochemical impedance spectroscopy, and giant magnetic impedance. Looking into the future, methods for AFP detection that are high sensitivity, long-term stability, low cost, and operation convenience will continue to be developed.

As a biomarker, alpha-fetoprotein (AFP) is valuable for detecting some tumors in men, non-pregnant women, and children. However, the detection sensitivity in some methods needs to be improved. Therefore, developing a simple, reliable, and sensitive detection method for AFP is important for non-malignant diseases. An aptamer binding was developed based on aggregation-induced emission luminogen (AIEgen) nanosphere labeled with Fe3O4@MPTMS@AuNPs. AFP was detected with a sandwich structure of AuNPs magnetic composite particles. An aggregation-induced emission (AIE) molecule and polystyrene (PS) nanosphere complex were assembled, enhancing the fluorescence and improving the sensitivity of detection. The limit of detection (LOD) was at a given level of 1.429 pg/mL, which can best be achieved in serum samples. Finally, the results obtained showed the complex to be promising in practical applications.

Mercury ions (Hg²⁺) are highly toxic and pose severe risks to human health and ecosystems, necessitating sensitive detection methods for environmental monitoring. Here, we report a paper-based graphene sensor functionalized with single-stranded DNA (ssDNA) probes for Hg²⁺ detection based on T-Hg²⁺-T coordination chemistry. To elucidate the effect of probe structure on sensing performance, we designed DNA constructs with varying numbers of guanine (G) bases (3–6, designated DNA2–DNA5) in the bridging fragment and systematically evaluated their influence on hairpin stability, Hg²⁺ binding affinity, and sensor response. The DNA3-based sensor (four G bases) exhibited optimal electronic stability and sensitivity, achieving a detection limit of 0.673 pM with effective real-time monitoring capability in aqueous media. These findings highlight the critical role of DNA sequence design in T-Hg²⁺-T-based biosensors and provide a promising strategy for sensitive and selective Hg²⁺ detection in environmental samples.

To enhance the sensitivity of graphene-DNA sensors for Hg²⁺ detection, a novel graphene nanoribbon-DNA sensor was fabricated using a template-assisted approach. Silicon nanowires served as templates to decorate the graphene device, followed by plasma etching to delineate graphene nanoribbons. After template removal, the resulting sensors based on silicon nanowire templates were successfully constructed. DNA sequences containing four guanine bases were conjugated with graphene sensors prepared using the templates. The carboxyl groups on the edges of the graphene nanoribbons were activated with EDC/NHS chemistry to facilitate covalent bonding with amino-modified DNA. The kinetic response and Hg²⁺ detection capability of the fabricated sensors were characterized using a semiconductor parameter analyzer. Results indicated that the silicon nanowire-templated graphene nanoribbon sensor exhibited high sensitivity, with a detection limit of 3.62 pM. This innovative approach further improved the sensitivity of graphene-DNA sensors for Hg²⁺ detection.