Synaptic plasticity constitutes a fundamental mechanism of neural systems. Rhythmic activities (e.g., θ and γ oscillations) play a critical role in modulating network plasticity efficiency in biological neural systems. However, the rules governing plasticity and adaptive regulation of in vitro cultured networks under structured electrical stimulation remain insufficiently characterized. To quantitatively investigate these regulatory effects within a highly controlled and low-interference environment, we utilized primary mice hippocampal neurons cultured on multielectrode arrays (MEAs) and executed two dedicated sets of experiments. (1) Spatiotemporal electrical stimulation paradigms, combined with connectivity analysis, revealed pronounced regulation effects of network plasticity. (2) Physiologically inspired rhythmic stimulation (θ: 7.8 Hz, γ: 40 Hz) with varying pulse repetitions was then applied. Although both rhythms induced distinct frequency-dependent plasticity modulation, the disparity between their modulatory effects progressively diminished with increasing stimulation pulse numbers, suggesting an intrinsic adaptive regulatory mechanism. Collectively, our findings characterize the effects of plasticity regulation and reveal the mechanisms underlying adaptive convergence in in vitro neuronal systems. These results advance the understanding of network plasticity, providing a technical foundation for functional shaping and modulation of in vitro neural networks while supporting future explorations into learning-oriented modulation.

Yeast biosensors represent a promising biotechnological innovation for ensuring the safety and quality of fermented beverages such as beer, wine, and kombucha. These biosensors employ genetically engineered yeast strains to detect specific contaminants, spoilage organisms, or hazardous compounds during fermentation or the final product. By integrating synthetic biology tools, researchers have developed yeast strains that can sense and respond to the presence of heavy metals (e.g., lead or arsenic), mycotoxins, ethanol levels, or unwanted microbial metabolites. When a target compound is detected, the biosensor yeast activates a reporter system, such as fluorescence, color change, or electrical signal, providing a rapid, visible, and cost-effective means of monitoring safety parameters. These biosensors offer several advantages: they can operate in real time, are relatively low-cost compared to conventional chemical analysis methods, and can be integrated directly into the fermentation system. Furthermore, as Saccharomyces cerevisiae is generally recognized as safe (GRAS), its use as a sensing platform aligns well with existing practices in beverage production. Yeast biosensors are being investigated for the early detection of contamination by spoilage microbes, such as Brettanomyces and lactic acid bacteria. These contaminants can alter the flavor profile and shorten the product’s shelf life. By providing timely feedback, these biosensor systems allow producers to intervene early, thereby reducing waste and enhancing consumer safety. In this work, we review the development and application of yeast-based biosensors as potential safeguards in fermented beverage production, with the overarching goal of contributing to the manufacture of safer and higher-quality products. Nevertheless, despite their substantial conceptual promise and encouraging experimental results, yeast biosensors remain confined mainly to laboratory-scale studies. A clear gap persists between their demonstrated potential and widespread industrial implementation, underscoring the need for further research focused on robustness, scalability, and regulatory integration.

Microparticle detection technology uses materials that can specifically recognize complex biostructures, such as antibodies and aptamers, as trapping agents. The development of antibody production technology and simplification of sensing signal output methods have facilitated commercialization of disposable biosensors, making rapid diagnosis possible. Although this contributed to the early resolution of pandemics, traditional biosensors face issues with sensitivity, durability, and rapid response times. We aimed to fabricate microspaces using metallic materials to further enhance durability of mold fabrication technologies, such as molecular imprinting. Low-damage metal deposition was performed on target protozoa and Norovirus-like particles (NoV-LPs) to produce thin metallic films that adhere to the material. The procedure for fitting the object into the bio structured space formed on the thin metal film took less than a minute, and sensitivity was 10 fg/mL for NoV-LPs. Furthermore, because it was a metal film, no decrease in reactivity was observed even when the same substrate was stored at room temperature and reused repeatedly after fabrication. These findings underscore the potential of integrating stable metallic structures with bio-recognition elements to significantly enhance robustness and reliability of environmental monitoring. This contributes to public health strategies aimed at early detection and containment of infectious diseases.

The reliance on unstable hydrogen peroxide (H2O2) adversely affects the robustness and simplicity of chemiluminescence (CL)-based immunoassays. We report a novel external H2O2-free Fenton CL system integrated into a highly sensitive non-enzymatic immunoassay for the detection of SARS-CoV-2 nucleoprotein, utilizing cuprous–polyethylenimine–lipoic acid nanoflowers (Cu(I)-PEI-LA-Ab NF) as a non-enzymatic tag. The signaling polymer (PEI-LA) was synthesized via EDC/NHS coupling, which conjugated approximately 550 LA units to the PEI backbone. This polymer formed antibody-conjugated NF with various metal ions, and the Cu(I)-based variant was selected for its intense and sustained CL with luminol. The mechanism relies on an in situ Fenton reaction, in which dissolved oxygen is reduced by Cu(I) to H2O2, which reacts with oxidized Cu(II), producing hydroxyl radicals that oxidize luminol. Direct calibration of the SARS-CoV-2 nucleoprotein fixed on microplate wells demonstrated excellent linearity in the range of 0.01–3.13 ng/mL (LOD = 3 pg/mL). In a final competitive immunoassay format for samples spiked with the antigen, a decreasing CL signal that correlated with increasing antigen concentration was obtained in the range of 0.1–20.0 ng/mL, achieving excellent recoveries that were favorable compared with those of the sandwich ELISA kit, establishing this H2O2-independent platform as a powerful and robust tool for clinical diagnostics.

Aquaculture is a crucial global food production sector that faces challenges in water quality management, food safety, and stress-related health concerns in aquatic species. Cortisol, a key stress biomarker in fish, and Escherichia coli (E. coli) contamination in bivalve mollusks are critical indicators that require sensitive and real-time detection methods. Liquid crystal (LC)-based immunosensors have emerged as a promising solution for detecting biological analytes due to their high sensitivity, rapid response, and label-free optical detection capabilities. Therefore, this study explores the development and application of LC-based immunosensors for the detection of cortisol in artificial and real recirculating aquaculture system (RAS) samples, as well as E. coli in real contaminated water and clam samples during the depuration processes of bivalve mollusks. The biosensors exhibited the capacity to detect cortisol with a response time in seconds and a limit of detection (LOD) of 0.1 ng/mL. Furthermore, they demonstrated specificity to cortisol when tested against different interfering substances, including testosterone, glucose, and cholesterol. Furthermore, it was possible to correlate cortisol concentrations in different filtration stages and track E. coli contamination during depuration. The results confirm the feasibility of LC-based immunosensors as a user-friendly, portable, and efficient diagnostic tool for aquaculture applications.

Surface-imprinted polymer (SIP)-based biomimetic sensors are promising for direct whole-bacteria detection; however, the commonly used fabrication approach (micro-contact imprinting) often suffers from limited imprint density, heterogeneous template distribution, and poor reproducibility. Here, we introduce a photolithography-defined master stamp featuring E. coli mimics, enabling high-density, well-oriented cavity arrays (3 × 107 imprints/cm2). Crucially, the cavity arrangement is engineered such that the SIP layer functions simultaneously as the bioreceptor and as a diffraction grating, enabling label-free optical quantification by reflectance changes without additional transduction layers. Finite-difference time-domain (FDTD) simulations are used to model and visualize the optical response upon bacterial binding. Proof-of-concept experiments using a differential two-well configuration confirm concentration-dependent detection of E. coli in PBS, demonstrating a sensitive, low-cost, and scalable sensing concept that can be readily extended to other bacterial targets by redesigning the photolithographic master.

Foodborne pathogens remain a major global concern, demanding rapid, accessible, and determination technologies. Conventional methods, such as culture assays and polymerase chain reaction, offer high accuracy but are time-consuming for on-site testing. This study presents a portable, smartphone-assisted dual-mode biosensor that combines colorimetric and photothermal speckle imaging for improved sensitivity in lateral flow assays (LFAs). The prototype device, built using low-cost components ($500), uses a Raspberry Pi for illumination control, image acquisition, and machine learning-based signal analysis. Colorimetric features were derived from normalized RGB intensities, while photothermal responses were obtained from speckle fluctuation metrics during periodic plasmonic heating. Multivariate linear regression, with and without LASSO regularization, was used to predict Salmonella concentrations. The comparison revealed that regularization did not significantly improve predictive accuracy indicating that the unregularized linear model is sufficient and that the extracted features are robust without complex penalization. The fused model achieved the best performance (R2 = 0.91) and consistently predicted concentrations down to a limit of detection (LOD) of 104 CFU/mL, which is one order of magnitude improvement of visual and benchtop measurements from previous work. Blind testing confirmed robustness but also revealed difficulty distinguishing between negative and 103 CFU/mL samples. This work demonstrates a low-cost, field-deployable biosensing platform capable of quantitative pathogen detection, establishing a foundation for the future deployment of smartphone-assisted, machine learning-enabled diagnostic tools for broader monitoring applications.

Automated sleep staging remains challenging due to the transitional nature of certain sleep stages, particularly N1. In this paper, we explore modulation spectrograms for automatic sleep staging to capture the transitional nature of sleep stages and compare them with conventional benchmark features, such as the Short-Time Fourier Transform (STFT) and the Continuous Wavelet Transform (CWT). We utilized a single-channel EEG (C4–M1) from the DREAMT dataset with subject-independent validation. We stratify participants by the Apnea–Hypopnea Index (AHI) into Normal, Mild, Moderate, and Severe groups to assess clinical generalizability. Our modulation-based framework significantly outperforms STFT and CWT in the Mild and Severe cohorts, while maintaining comparable high performance in the Normal and Moderate AHI groups. Notably, the proposed framework maintained robust performance in severe apnea cohorts, effectively mitigating the degradation observed in standard time–frequency baselines. These findings demonstrate the effectiveness of modulation spectrograms for sleep staging while emphasizing the importance of medical stratification for reliable outcomes in clinical populations.

The integration of flexible electronics and machine learning (ML) algorithms has become a revolutionary force driving the field of intelligent sensing, giving rise to a new generation of intelligent devices and systems. This article provides a systematic review of core technologies and practical applications of ML in flexible electronics. It focuses on analyzing the theoretical frameworks of algorithms such as the Long Short-Term Memory Network (LSTM), Convolutional Neural Network (CNN), and Reinforcement Learning (RL) in the intelligent processing of sensor signals (IPSS), multimodal feature extraction (MFE), process defect and anomaly detection (PDAD), and data compression and edge computing (DCEC). This study explores the performance advantages of these technologies in optimizing signal analysis accuracy, compensating for interference in high-noise environments, optimizing manufacturing process parameters, etc., and empirically analyzes their potential applications in wearable health monitoring systems, intelligent control of soft robots, performance optimization of self-powered devices, and intelligent perception of epidermal electronic systems.

Plasmonic nanoparticles (NPs) exhibit exceptional optical and electromagnetic (EM) properties that are, however, confined to their near–field region, limiting effective interactions with non-adsorbed species. Metal–organic frameworks (MOFs), renowned for their high surface area and tunable pores, provide an ideal complement through surface enrichment and subsequent molecular enrichment within their pores. The integration of plasmonic NPs with MOFs into nanohybrids overcomes this spatial constraint. This architectural synergy creates a synergistic effect, yielding properties superior to either component alone. This review summarizes recent advances in NP–MOF nanohybrids, with a focus on synthesis strategies for diverse architectures and their emergent functionalities. We highlight how this synergistic effect enables breakthrough applications in chemical sensing, cancer therapy, and catalysis. Finally, we conclude our discussion and present a critical outlook that explores the challenges and future opportunities in the design and applications of NP–MOF nanohybrids.