Biosensors

3 pages, 135 KB

Open AccessEditorial

Advanced Immunoassays and Biosensing: From Design to Development

by Dongyang Li, Xu Wang and Juan Pablo Salvador

Biosensors 2025, 15(12), 822; https://doi.org/10.3390/bios15120822 - 18 Dec 2025

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Over the past decade, the field of immunoassays and biosensing has undergone remarkable expansion, driven by the urgent demand for sensitive, rapid, and reliable detection technologies across biomedical, environmental, and food safety applications [...] Full article

(This article belongs to the Special Issue Immunoassays and Biosensing)

17 pages, 2257 KB

Open AccessArticle

Rapid Visual Detection of Mycoplasma Hominis Using an RPA-CRISPR/Cas12a Assay

by Jie Chen, Shutao Liu, Sunyi Chen, Jingwen Mai, Maiwula Abudukadi, Yao Chen, Jie Lu, Guanglei Li and Chenchen Ge

Biosensors 2025, 15(12), 821; https://doi.org/10.3390/bios15120821 - 18 Dec 2025

Viewed by 302

Abstract

Mycoplasma hominis (MH) is a prevalent opportunistic pathogen that is strongly associated with a wide range of urogenital tract infections and severe adverse pregnancy outcomes in clinical settings. Current MH detection methods, including microbial culture and qPCR, are time-consuming and rely on complex [...] Read more.

Mycoplasma hominis (MH) is a prevalent opportunistic pathogen that is strongly associated with a wide range of urogenital tract infections and severe adverse pregnancy outcomes in clinical settings. Current MH detection methods, including microbial culture and qPCR, are time-consuming and rely on complex equipment, making them unsuitable for scenarios requiring rapid or simplified testing. In this study, we developed a visual readout biosensing platform by synergistically integrating recombinase polymerase amplification (RPA), CRISPR/Cas12a-mediated target nucleic acid recognition, and lateral flow biosensors for the rapid, sensitive, and specific identification of MH. The assay specifically targets the MH-specific 16S rRNA gene, achieving a limit of detection as low as 2 copies/reaction of recombinant plasmid containing the target gene with a total assay time of 60 min. Critical reaction parameters, including Cas12a-crRNA molar ratio, volume of RPA amplicon input, and Cas12a cleavage time, were systematically optimized to maximize the biosensor’s response efficiency and detection reliability. The platform exhibited exceptional specificity, with no cross-reactivity observed against common co-occurring urogenital pathogens, and effectively minimized aerosol contamination risks via a rigorous decontamination workflow. Furthermore, this work represents the first documented implementation of a contamination-control protocol for an MH-specific CRISPR-LFA assay. Notably, testing results from 18 clinical samples demonstrated the high specificity of this assay, highlighting its promising potential for clinical application. Full article

(This article belongs to the Special Issue Point-of-Care Testing Using Biochemical Sensors for Health and Safety)

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16 pages, 1136 KB

Open AccessArticle

Development of Metabolite-Responsive Transcription Factor Systems as Modular Platforms for Gene Expression Control

by Haekang Ji, Jiwon Lee, Kyeongseok Song, Yangwon Jeon, Geupil Jang and Youngdae Yoon

Biosensors 2025, 15(12), 820; https://doi.org/10.3390/bios15120820 - 18 Dec 2025

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Abstract

Traditional inducible systems typically induce the simultaneous expression of all genes controlled by similar promoters, thereby limiting their use. In this study, we used two metabolite-inducible systems, MarR from the Escherichia coli mar operon and TtgR from the Pseudomonas putida ttg operon, to [...] Read more.

Traditional inducible systems typically induce the simultaneous expression of all genes controlled by similar promoters, thereby limiting their use. In this study, we used two metabolite-inducible systems, MarR from the Escherichia coli mar operon and TtgR from the Pseudomonas putida ttg operon, to assess their use as gene regulation platforms beyond reporter assays. Ligand-dependent transcription was validated using eGFP. The reporter was replaced with two flavonoid O-methyltransferases (OMTs), ROMT-9 and SOMT-2, under transcription factor (TF)-specific promoters. In E. coli, both systems enabled in using HPLC. TF-based expression did not impact enzyme activity. Induction with salicylic acid (MarR) produced stronger gains than that with 4′-hydroxyflavanone (TtgR), although the overall fold-changes in product levels were regulated by basal (leaky) expression. Thus, although transcriptional control was robust, enzymatic regulation was less stringent, highlighting the necessity for genetic engineering of components, including TFs, promoters, transcription factor binding sites, and ribosome binding sites, to reduce leakiness and expand the dynamic range. Overall, these orthogonal and modular TF-based systems offer a framework for independent and inducible control of multiple genes, with potential applications in biosensing, metabolic engineering, and programmable pathway design. Full article

(This article belongs to the Special Issue Microbial Biosensor: From Design to Applications—2nd Edition)

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29 pages, 8564 KB

Open AccessReview

Comprehensive Review on DNA Hydrogels and DNA Origami-Enabled Wearable and Implantable Biosensors

by Man Li and Joonho Bae

Biosensors 2025, 15(12), 819; https://doi.org/10.3390/bios15120819 - 18 Dec 2025

Viewed by 604

Abstract

DNA nanoparticles have emerged as potent platforms for wearable and implantable biosensors owing to their molecular programmability, biocompatibility, and structural precision. This study delineates two principal categories of DNA-based sensing materials, DNA hydrogels and DNA origami, and encapsulates their fabrication methodologies, sensing mechanisms, [...] Read more.

DNA nanoparticles have emerged as potent platforms for wearable and implantable biosensors owing to their molecular programmability, biocompatibility, and structural precision. This study delineates two principal categories of DNA-based sensing materials, DNA hydrogels and DNA origami, and encapsulates their fabrication methodologies, sensing mechanisms, and applications at the device level. DNA hydrogels serve as pliable, aqueous signal transduction mediums exhibiting stimulus-responsive characteristics, facilitating applications such as sweat-based cytokine detection with limits of detection as low as pg·mL⁻¹ and microneedle-integrated hydrogels for femtomolar miRNA sensing. DNA origami offers nanometer-scale spatial precision that improves electrochemical, optical, and plasmonic biosensing, as shown by origami-facilitated luminous nucleic acid detection and ultrasensitive circulating tumor DNA assays with fM-level sensitivity. Emerging integration technologies, such as flexible electronics, microfluidics, and wireless readout, are examined, alongside prospective developments in AI-assisted DNA design and materials produced from synthetic biology. This study offers a thorough and practical viewpoint on the progression of DNA nanotechnology for next-generation wearable and implantable biosensing devices. Full article

(This article belongs to the Section Wearable Biosensors)

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13 pages, 939 KB

Open AccessArticle

Temporal Changes in Brain Light Scattering and Its Independent Variables Within 2 Days of Life

by Kennosuke Tsuda, Sachiko Iwata, Shinji Saitoh and Osuke Iwata

Biosensors 2025, 15(12), 818; https://doi.org/10.3390/bios15120818 - 17 Dec 2025

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Abstract

The reduced scattering coefficient (μ_s′), measured using time-resolved near-infrared spectroscopy (TR-NIRS) has been linked to brain water diffusion assessed by diffusion tensor imaging, suggesting its potential as a bedside marker of cerebral microstructure. However, the physiological determinants of μ_s′ [...] Read more.

The reduced scattering coefficient (μ_s′), measured using time-resolved near-infrared spectroscopy (TR-NIRS) has been linked to brain water diffusion assessed by diffusion tensor imaging, suggesting its potential as a bedside marker of cerebral microstructure. However, the physiological determinants of μ_s′ and its early postnatal changes remain unclear. This study examined clinical associations with cerebral μ_s′ in healthy term newborn infants during the first 2 postnatal days. Eighteen newborn infants underwent TR-NIRS at 6 and 36 h postnatally. Associations between μ_s′ and 14 clinical variables were analysed using generalised estimating equations. Median μ_s′ was 7.395 cm⁻¹ (IQR: 6.140–8.159) at 6 h and 7.112 cm⁻¹ (IQR: 6.473–7.410) at 36 h, with no significant difference (p = 0.327). Male sex was associated with higher μ_s′ (regression coefficient = 0.895, p = 0.007), whereas caesarean delivery (regression coefficient = −0.969, p = 0.012) was associated with lower μ_s′. A significant interaction between caesarean delivery and postnatal age indicated that the negative effect diminished between 6 and 36 h after birth (difference = 0.057, p = 0.016). These findings suggest delivery mode transiently influences brain scattering, whereas the effect of sex remains stable, supporting further investigation of TR-NIRS as an acute-phase cerebral marker. Full article

(This article belongs to the Section Optical and Photonic Biosensors)

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12 pages, 2246 KB

Open AccessArticle

Peptide-Based Plasmon-Enhanced Spectroscopic Immunoassay to Detect Immunity Against Cytomegalovirus

by Aruna Chandra Singh, Clara Sidhoum, Hugo Payen, Divya Balakrishnan, Saulius Juodkazis, Thomas Østerbye and Sivashankar Krishnamoorthy

Biosensors 2025, 15(12), 817; https://doi.org/10.3390/bios15120817 - 17 Dec 2025

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Abstract

Sensors to monitor the immune status of an individual play a crucial role in understanding the acquired immunity or signs of a latent infection. Such sensors can be an effective tool to manage infection and to design treatment options in vulnerable populations. We [...] Read more.

Sensors to monitor the immune status of an individual play a crucial role in understanding the acquired immunity or signs of a latent infection. Such sensors can be an effective tool to manage infection and to design treatment options in vulnerable populations. We demonstrate here highly sensitive detection of acquired immunity to Cytomegalovirus CMV by detection of anti-CMV antibodies using plasmon-enhanced fluorescence (PEF). The PEF sensors leverage plasmonic enhancement from a high density of intense electromagnetic hotspots in self-assembly-derived gold nanopillar arrays. Comparing PEF assays with assays on a planar surface plasmon resonance sensor shows the PEF sensors to be sensitive to a small fraction of the antibodies on the surface. The detection scheme deploys peptide monolayers with specific affinity to anti-CMV antibodies to capture them onto the sensor surfaces. The results of the assay on the PEF sensor reveal high promise for sensors with miniaturized sensing footprints, ease of spatial multiplexing, high sensitivity, and quick response times. The developments are readily applicable to a range of other diagnostic contexts where peptide–protein interactions and self-assembly-derived PEF sensors can be leveraged. Full article

(This article belongs to the Special Issue Periodic Man-Made Nanostructure-Based Biosensors)

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17 pages, 2960 KB

Open AccessArticle

Paper-Based Colorimetric pH Test Strip Using Bio-Derived Dyes

by Aramis A. Sánchez, Darwin Castillo, Grettel Riofrío-Cabrera, Greysy Jaramillo and Vasudevan Lakshminarayanan

Biosensors 2025, 15(12), 816; https://doi.org/10.3390/bios15120816 - 16 Dec 2025

Viewed by 447

Abstract

Natural dyes have emerged as a promising alternative to synthetic dyes for industrial applications due to their advantages, namely, easy availability, low cost, and environmental friendliness. In this sense, natural dyes, due to their potential to react over the pH range, could offer [...] Read more.

Natural dyes have emerged as a promising alternative to synthetic dyes for industrial applications due to their advantages, namely, easy availability, low cost, and environmental friendliness. In this sense, natural dyes, due to their potential to react over the pH range, could offer an alternative to conventional pH measuring techniques for industrial products, such as potentiometers, sensors, or indicator drops. Therefore, this project aims to evaluate the potential of several natural organic dyes in response to changes in pH and develop an indicator for determining pH grades. We extracted and analyzed the pigments of forty natural vegetable species using two extraction methods with a mixture of solvents, specifically 70% MeOH/30% H₂O. The results find that pigments of cabbage, hibiscus flower, radish, and turmeric in their dry state exhibit the best reaction over a broad pH range, and color can be easily distinguished according to its level. These findings demonstrate the potential of natural dyes as a novel approach for pH verification, providing a sustainable and cost-effective alternative to conventional techniques. Full article

(This article belongs to the Section Biosensor Materials)

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20 pages, 19282 KB

Open AccessArticle

Single-Exosome SERS Detection by Means of a Flexible Metasurface

by Konstantin Mochalov, Denis Korzhov, Milena Shestopalova, Andrey Ivanov, Konstantin Afanasev, Alexander Smyk, Alexander Shurygin and Andrey K. Sarychev

Biosensors 2025, 15(12), 815; https://doi.org/10.3390/bios15120815 - 15 Dec 2025

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Abstract

Single exosomes are detected via surface-enhanced Raman scattering (SERS) due to electromagnetic field accumulation on a specially designed flexible metasurface. This metasurface is a modulated silver nanofilm deposited on a thin, flexible plastic substrate. An explicit Equation for calculating the local electric field [...] Read more.

Single exosomes are detected via surface-enhanced Raman scattering (SERS) due to electromagnetic field accumulation on a specially designed flexible metasurface. This metasurface is a modulated silver nanofilm deposited on a thin, flexible plastic substrate. An explicit Equation for calculating the local electric field is given. The field reaches extremely high values under plasmon resonance conditions and fills the depressions of the metasurface. The thin, flexible metasurface can be incorporated into automated Lab-On-Chip analytical systems and used for spectroscopic studies of exosomes. We propose a method to distinguish individual exosomes from the HEK293T cell line on the metasurface and then obtain and assign their SERS spectra. An important advantage of the plasmonic metasurface presented in this work is its spatial complementarity to exosomes and other vesicle-like objects. The plasmonic metasurface is fabricated using holographic lithography and further investigated using a correlation approach combining atomic force microscopy, scanning spreading resistance microscopy, and surface-enhanced spectroscopy. Full article

(This article belongs to the Special Issue Raman Scattering-Based Biosensing)

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14 pages, 2204 KB

Open AccessArticle

Quantitative Detection of Salmonella Typhimurium in Ground Chicken Using a Surface Plasmon Resonance (SPR) Biosensor

by Sandhya Thapa and Fur-Chi Chen

Biosensors 2025, 15(12), 814; https://doi.org/10.3390/bios15120814 - 15 Dec 2025

Viewed by 310

Abstract

Regulatory agencies worldwide have implemented stringent measures to monitor and reduce Salmonella contamination in poultry products. Rapid quantitative detection methods enable producers to identify contamination early, implement corrective actions, and enhance food safety. This study aimed to develop and optimize a surface plasmon [...] Read more.

Regulatory agencies worldwide have implemented stringent measures to monitor and reduce Salmonella contamination in poultry products. Rapid quantitative detection methods enable producers to identify contamination early, implement corrective actions, and enhance food safety. This study aimed to develop and optimize a surface plasmon resonance (SPR) biosensor for the quantitative detection of Salmonella Typhimurium in ground chicken. The sensor surface was functionalized with a well-characterized monoclonal antibody specific to Salmonella flagellin, and an SPR workflow was established for quantitative analysis. Ground chicken samples were inoculated with four S. Typhimurium strains at contamination levels ranging from −0.5 to 3.5 Log CFU/g and enriched at 42 °C for 10 or 12 h prior to SPR analysis. Contamination levels were confirmed using the Most Probable Number (MPN) method. Linear regression analysis indicated that optimal quantification was achieved after 10 h of enrichment (R² ≥ 0.86), whereas extended enrichment (12 h) did not improve performance. The limit of quantification (LOQ) was below 1 CFU/g. A strong positive correlation (R² ≥ 0.85) was observed between SPR and MPN results, demonstrating consistency between the two methods. These findings highlight SPR as a rapid, reliable, and cost-effective alternative to conventional methods for Salmonella quantification. By delivering accurate results within a single day, SPR enhances testing efficiency and supports the production of safer poultry products, thereby reducing public health risks associated with Salmonella contamination. Full article

(This article belongs to the Special Issue Advances in Biosensors for Food Safety, Environmental Monitoring, and Biomedical Applications)

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12 pages, 1115 KB

Open AccessArticle

Click Detect: A Rapid and Sensitive Assay for Shiga Toxin 2 Detection

by Benjamin M. Thomas, Emma L. Webb, Katherine L. Yan, Alexi M. Fernandez and Zhilei Chen

Biosensors 2025, 15(12), 813; https://doi.org/10.3390/bios15120813 - 14 Dec 2025

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Abstract

Shiga toxin-producing Escherichia coli (STEC) is a major foodborne pathogen, responsible for severe gastrointestinal disease and hemolytic uremic syndrome (HUS). Here, we report Click Detect, a novel diagnostic platform that leverages click display to efficiently produce sensing probes for sandwich-style antigen detection. Click [...] Read more.

Shiga toxin-producing Escherichia coli (STEC) is a major foodborne pathogen, responsible for severe gastrointestinal disease and hemolytic uremic syndrome (HUS). Here, we report Click Detect, a novel diagnostic platform that leverages click display to efficiently produce sensing probes for sandwich-style antigen detection. Click display is an in vitro protein display technology that generates uniform and covalently linked protein–cDNA conjugates in a simple one-pot reaction format within 2 h. The captured sensing probe can be quantified by standard nucleic acid amplification assays. Using click displayed DARPin (D_#20) as the sensing probe and a high-affinity nanobody (N_G1) as the capture reagent, Click Detect reliably detected Shiga toxin 2 (Stx2) at 600 fM by quantitative PCR (qPCR) and 6 pM by loop-mediated isothermal amplification (LAMP). The assay maintained comparable sensitivity in matrices containing up to 40% public swimming pool water or lettuce extract, highlighting robustness for real-world surveillance applications. Key advantages of Click Detect include simple, rapid, and cost-effective (~USD 0.04 per assay) sensing probe preparation, as well as a versatile plug-and-play probe format for detecting other targets. We believe that Click Detect has great potential as a novel sensing platform for food/environmental monitoring and point-of-care diagnostics, with potentially broad applicability to other toxins and protein targets. Full article

(This article belongs to the Special Issue Sensors for Detection of Bacteria and Their Toxins)

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21 pages, 3364 KB

Open AccessArticle

Advancing Lateral Flow Detection in CRISPR/Cas12a Systems Through Rational Understanding and Design Strategies of Reporter Interactions

by Irina V. Safenkova, Maria V. Kamionskaya, Dmitriy V. Sotnikov, Sergey F. Biketov, Anatoly V. Zherdev and Boris B. Dzantiev

Biosensors 2025, 15(12), 812; https://doi.org/10.3390/bios15120812 - 13 Dec 2025

Viewed by 543

Abstract

CRISPR/Cas12a systems coupled with lateral flow tests (LFTs) are a promising route to rapid, instrument-free nucleic acid diagnostics due to conversion target recognition into a simple visual readout via cleavage of dual-labeled single-stranded DNA reporters. However, the conventional CRISPR/Cas12a–LFT system is constructed in [...] Read more.

CRISPR/Cas12a systems coupled with lateral flow tests (LFTs) are a promising route to rapid, instrument-free nucleic acid diagnostics due to conversion target recognition into a simple visual readout via cleavage of dual-labeled single-stranded DNA reporters. However, the conventional CRISPR/Cas12a–LFT system is constructed in a format where the intact reporter should block nanoparticle conjugate migration and can produce false-positive signals and shows strong dependence on component stoichiometry and kinetics. Here, we present the first combined experimental and theoretical analysis quantifying these limitations and defining practical solutions. The experimental evaluation included 480 variants of LFT configuration with reporters differing in the concentration of interacting components and the kinetic conditions of the interactions. The most influential factor leading to 100% false-positive results was insufficient interaction time between the components; pre-incubation of the conjugate with the reporter for 5 min eliminated these artifacts. Theoretical analysis of the LFT kinetics based on a mathematical model confirmed kinetic constraints at interaction times below a few minutes, which affect the detectable signal. Reporter concentration and conjugate architecture represented the second major factors: lowering reporter concentration to 20 nM and using smaller gold nanoparticles with multivalent fluorescent reporters markedly improved sensitivity. The difference in sensitivity between various LFT configurations exceeded 50-fold. The combination of identified strategies eliminated false-positive reactions and enabled the detection of up to 20 pM of DNA target (the hisZ gene of Erwinia amylovora, a bacterial phytopathogen). The strategies reported here are general and readily transferable to other DNA targets and CRISPR/Cas12a amplification-free diagnostics. Full article

(This article belongs to the Special Issue CRISPR/Cas System-Based Biosensors)

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52 pages, 5061 KB

Open AccessSystematic Review

Personal Glucose Meter: Biosensing Platforms for Environmental Toxicants

by Elena Dorozhko, Anna Solomonenko, Alena Koltsova, Elena Korotkova, Ekaterina Mikhnevich, Mrinal Vashisth, Pradip Kar, Amrit Hui and Muhammad Saqib

Biosensors 2025, 15(12), 811; https://doi.org/10.3390/bios15120811 - 13 Dec 2025

Viewed by 426

Abstract

The detection of environmental toxicants is transitioning from centralized laboratory methods to decentralized, point-of-care (POC) monitoring. A highly innovative approach in this field is the repurposing of commercially available, low-cost, and portable personal glucose meters (PGMs) as universal biosensing platforms. This strategy leverages [...] Read more.

The detection of environmental toxicants is transitioning from centralized laboratory methods to decentralized, point-of-care (POC) monitoring. A highly innovative approach in this field is the repurposing of commercially available, low-cost, and portable personal glucose meters (PGMs) as universal biosensing platforms. This strategy leverages the widespread availability and ease of use of PGMs to develop rapid, on-site detection methods for a wide array of non-glucose targets, significantly reducing both cost and development time. This systematic review comprehensively examines the various strategies employed to adapt PGMs for the detection of a wide array of ecotoxicants, including chemical targets (antibiotics, mycotoxins, pesticides, heavy metals, persistent organic pollutants) and biological ones (pathogenic bacteria, and viruses). The systematic review critically evaluates different sensor designs, highlighting that while aptamer-based and non-enzymatic biosensors offer advantages in stability and cost, antibody-based sensors provide high specificity. A significant finding is the persistent trade-off between analytical sensitivity and practical field deployment; many of the most sensitive assays require multi-step procedures, precise temperature control, magnetic separation, centrifugation, and the use of additional equipment, factors that undermine true POC utility. To address this gap, we propose four essential criteria for POC readiness: (i) ambient-temperature operation, (ii) no reliance on magnetic or centrifugal separation, (iii) total assay time, and (iv) robustness in complex environmental matrices. This systematic review confirms the feasibility of this approach across a broad spectrum of targets. However, the key challenge for future research lies in simplifying the assay protocols, eliminating cumbersome sample preparation steps, and enhancing robustness to make these biosensors truly practical for routine, on-site environmental monitoring. Full article

(This article belongs to the Special Issue Electrochemical Biosensors in Healthcare Services)

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16 pages, 2599 KB

Open AccessArticle

Rapid On-Site Detection of Zearalenone in Maize Using a Colloidal Gold Immunochromatographic Strip

by Mengjiao Wu, Xiaofei Hu, Lu Fan, Bo Wan, Yaning Sun, Yunrui Xing, Lianjun Song, Xianqing Huang, Mei Hu and Gaiping Zhang

Biosensors 2025, 15(12), 810; https://doi.org/10.3390/bios15120810 - 12 Dec 2025

Viewed by 316

Abstract

Zearalenone (ZEN), a stable mycotoxin with estrogenic activity produced by various Fusarium species, poses a serious food safety risk. To facilitate the rapid, sensitive, on-site detection of ZEN in maize and ensure consumer dietary safety, a colloidal gold immunochromatographic assay (CG-ICA) based on [...] Read more.

Zearalenone (ZEN), a stable mycotoxin with estrogenic activity produced by various Fusarium species, poses a serious food safety risk. To facilitate the rapid, sensitive, on-site detection of ZEN in maize and ensure consumer dietary safety, a colloidal gold immunochromatographic assay (CG-ICA) based on a monoclonal antibody was established. ZEN was converted via oxime derivatization into hapten ZAN-O, which was conjugated to a carrier protein to prepare an immunogen for producing a highly specific and sensitive monoclonal antibody. Then, the antibody was conjugated into colloidal gold nanoparticles (AuNPs) and used as capture bioprobes of the CG-ICA test strip. The highly sensitive and specific detection platform was established through systematic optimization of pH value, coating antigen concentration, antibody-labeling dosage, incubation time, and strip assembly conditions. Under optimized conditions, the strip exhibited a detection limit of 11.79 pg/mL and an IC₅₀ of 99.06 pg/mL, with a linear detection range of 13.40–732.48 pg/mL. In addition, the anti-interference capability assay demonstrated that the developed test strip possessed excellent specificity. In spiked maize samples, the CG-ICA test strip demonstrated recoveries ranging from 85.36% to 98.86%, with relative standard deviations (RSDs) below 10%. Thus, the CG-ICA strip provides a rapid, sensitive, and robust on-site tool for ZEN screening in maize, and can be adapted to other hazards by simply switching the antibody. Full article

(This article belongs to the Section Biosensor and Bioelectronic Devices)

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74 pages, 18738 KB

Open AccessReview

Nanoparticle Detection in Biology and Medicine: A Review

by Olga A. Kolesnikova, Dmitry A. Shikvin, Arina O. Antonova, Anna M. Iureva, Elena N. Komedchikova, Anastasiia S. Obozina, Valeryia S. Kachan, Anna V. Svetlakova, Ilya D. Kukushkin and Victoria O. Shipunova

Biosensors 2025, 15(12), 809; https://doi.org/10.3390/bios15120809 - 11 Dec 2025

Cited by 1 | Viewed by 1577

Abstract

Background/Objectives: Nanoparticles have emerged as indispensable tools in modern biomedicine, enabling precise diagnostics, targeted therapy, and controlled drug delivery. Despite their rapid progress, the translation of nanoparticle-based systems critically depends on the ability to detect, quantify, and track them across complex biological environments. [...] Read more.

Background/Objectives: Nanoparticles have emerged as indispensable tools in modern biomedicine, enabling precise diagnostics, targeted therapy, and controlled drug delivery. Despite their rapid progress, the translation of nanoparticle-based systems critically depends on the ability to detect, quantify, and track them across complex biological environments. Over the past two decades, a wide spectrum of detection modalities has been developed, encompassing optical, magnetic, acoustic, nuclear, cytometric, and mass spectrometric principles. Yet, no comprehensive framework has been established to compare these methods in terms of sensitivity, spatial resolution, and clinical applicability. Methods: Here we show a systematic analysis of all broadly applicable nanoparticle detection strategies, outlining their mechanisms, advantages, and drawbacks, and providing illustrative examples of practical applications. Results: This comparison reveals that each modality occupies a distinct niche: optical methods offer high sensitivity but limited penetration depth; magnetic and acoustic modalities enable repeated non-invasive tracking; nuclear imaging ensures quantitative, whole-body visualization; and invasive biochemical or histological assays achieve ultimate detection limits at the cost of tissue integrity. These findings redefine how each technique contributes to nanoparticle biodistribution and mechanistic studies, clarifying which are best suited for translational and clinical use. Conclusions: Placed in a broader context, this review bridges fundamental nanotechnology with biomedical applications, outlining a unified methodological framework that will guide the rational design, validation, and clinical implementation of nanoparticle-based therapeutics and diagnostics. By synthesizing the field into a single comparative framework, it also provides an accessible entry point for newcomers in nanotechnology and related biomedical sciences. Full article

(This article belongs to the Section Biosensors and Healthcare)

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26 pages, 3841 KB

Open AccessReview

Polymer-Mediated Signal Amplification Mechanisms for Bioelectronic Detection: Recent Advances and Future Perspectives

by Ying Sun and Dan Gao

Biosensors 2025, 15(12), 808; https://doi.org/10.3390/bios15120808 - 11 Dec 2025

Viewed by 496

Abstract

In recent years, polymer-mediated signal amplification has drawn wide attention in bioelectronic sensing. With the rapid progress of biosensing and flexible electronics, polymers with excellent electron–ion transport properties, tunable molecular structures, and good biocompatibility have become essential materials for enhancing detection sensitivity and [...] Read more.

In recent years, polymer-mediated signal amplification has drawn wide attention in bioelectronic sensing. With the rapid progress of biosensing and flexible electronics, polymers with excellent electron–ion transport properties, tunable molecular structures, and good biocompatibility have become essential materials for enhancing detection sensitivity and interfacial stability. However, current sensing systems still face challenges such as signal attenuation, surface fouling, and multi-component interference in complex biological environments, limiting their use in medical diagnosis and environmental monitoring. This review summarizes the progress of conductive polymers, molecularly imprinted polymers, hydrogels, and composite polymers in medical diagnosis, food safety, and environmental monitoring, focusing on their signal amplification mechanisms and structural optimization strategies in electronic transport regulation, molecular recognition enhancement, and antifouling interface design. Overall, polymers improve detection performance through interfacial electronic reconstruction and multidimensional synergistic amplification, offering new ideas for developing highly sensitive, stable, and intelligent biosensors. In the future, polymer-based amplification systems are expected to expand in multi-parameter integrated detection, long-term wearable monitoring, and in situ analysis of complex samples, providing new approaches to precision medicine and sustainable environmental health monitoring. Full article

(This article belongs to the Special Issue Polymers-Based Biosensors and Bioelectronics: Designs and Applications)

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18 pages, 2719 KB

Open AccessArticle

A Novel Diagnostic Tool for West Nile Virus Lineage 1a and 2 Using a CRISPR-Cas12a System

by Soo Bin Hwang, Yoon-Jae Song and Pil-Gu Park

Biosensors 2025, 15(12), 807; https://doi.org/10.3390/bios15120807 - 10 Dec 2025

Viewed by 472

Abstract

The West Nile Virus (WNV), transmitted by Culex mosquitoes as a major vector, has been reported worldwide. Also, West Nile neuroinvasive disease (WNND) caused by WNV lineage 1a and 2 neuroinvasive infections has been constantly reported with high fatality rates. Nevertheless, there are [...] Read more.

The West Nile Virus (WNV), transmitted by Culex mosquitoes as a major vector, has been reported worldwide. Also, West Nile neuroinvasive disease (WNND) caused by WNV lineage 1a and 2 neuroinvasive infections has been constantly reported with high fatality rates. Nevertheless, there are no treatments and vaccinations, so diagnosis in the early stages is important. Recently, a molecular diagnostic technique using DNA endonuclease-targeted CRISPR trans reporter (DETECTR) with the CRISPR-Cas12a system integrated with isothermal nucleic acid amplification has newly emerged. In this study, we designed a 2-Step WNV DETECTR with reverse transcription–recombinase polymerase amplification (RT-RPA) for rapid and sensitive WNV diagnosis. It successfully detected down to 1.0 × 10² RNA copies for both WNV lineage 1a and 2 with demonstrating similar sensitivity to qRT-PCR without cross-reactivity to other viruses. Additionally, we designed a 1-Step WNV DETECTR, incorporating all processing steps into a single tube, capable of detecting down to 1.0 × 10³ RNA copies for both lineages. Furthermore, we developed a more streamlined method, the 1-Step with Filter WNV DETECTR, which achieved detection limits comparable to the 2-Step method, while reducing the processing time by 5 min. This study also explored the potential of the Punch-it™ NA-Sample Kit as an efficient alternative lysis method by comparing the detection differences across various lysis methods. Through this method, we achieved rapid and simple amplification and detection processes suitable for field diagnostics with high specificity and sufficient sensitivity. Therefore, DETECTR methods presented themselves as promising alternatives to conventional diagnostic tools, potentially overcoming financial and technical constraints in diverse medical settings. Full article

(This article belongs to the Section Biosensors and Healthcare)

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18 pages, 2816 KB

Open AccessArticle

Electrochemical Detection of Aβ42 and Aβ40 at Attomolar Scale via Optimised Antibody Loading on Pyr-NHS-Functionalised 3D Graphene Foam Electrodes

by Muhsin Dogan, Sophia Nazir, David Jenkins, Yinghui Wei and Genhua Pan

Biosensors 2025, 15(12), 806; https://doi.org/10.3390/bios15120806 - 10 Dec 2025

Viewed by 377

Abstract

Alzheimer’s Disease (AD) is one of the most commonly seen neurodegenerative disorders, where early detection of its biomarkers is crucial for effective management. Conventional diagnostic methods are often expensive, time-consuming, and highly complex, which highlights an urgent need for point-of-care biosensing technology. In [...] Read more.

Alzheimer’s Disease (AD) is one of the most commonly seen neurodegenerative disorders, where early detection of its biomarkers is crucial for effective management. Conventional diagnostic methods are often expensive, time-consuming, and highly complex, which highlights an urgent need for point-of-care biosensing technology. In this work, we developed assays on three-dimensional (3D) graphene foam electrodes by functionalising them with a 1-Pyrenebutyric acid N-hydroxysuccinimide ester (Pyr-NHS) to enable effective antibody immobilisation for the detection of amyloid beta peptides (Aβ42 and Aβ40), key biomarkers for AD. Pyr-NHS linkers were used for stable functionalisation, followed by binding with Aβ42 and Aβ40 antibodies, and then bovine serum albumin (BSA) was employed as a blocking agent to minimise non-specific bindings on the electrode surface. Differential Pulse Voltammetry (DPV) measurements showed satisfactory stability over 12 days (RDS upper limit was <10%) and highly sensitive and specific detection of Aβ42 and Aβ40, with insignificant interference of tau217 protein. The biosensor exhibited a low limit of detection (LOD) with 252 aM for Aβ42 and 395 aM for Aβ40, covering 0.125 fM–1 nM and 0.125 fM–100 pM linear ranges, respectively. Further validation was conducted on spiked-diluted human plasma. This excellent analytical performance was attributed to the stable Pyr-NHS functionalisation, the 3D graphene foam enabling superior conductivity and a larger surface area on the working electrode, and the optimisation of antibody concentration for immobilisation. These promising results suggest that 3D graphene foam-based biosensors have considerable potential for early detection of AD biomarkers and developing cost-effective, portable, and reliable point-of-care devices. Full article

(This article belongs to the Section Biosensor and Bioelectronic Devices)

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33 pages, 5719 KB

Open AccessArticle

Transparent PEDOT:PSS/PDMS Leaf Tattoos for Multiplexed Plant Health Monitoring and Energy Harvesting

by Antonio Ruiz-Gonzalez, Harriet Kempson and Jim Haseloff

Biosensors 2025, 15(12), 805; https://doi.org/10.3390/bios15120805 - 9 Dec 2025

Viewed by 460

Abstract

The development of non-invasive sensors for individualised plant monitoring has become essential in smart farming to increase crop production. However current approaches are focused on the measurement of soil parameters instead, which cannot provide direct information about plant health. Moreover, equipment used for [...] Read more.

The development of non-invasive sensors for individualised plant monitoring has become essential in smart farming to increase crop production. However current approaches are focused on the measurement of soil parameters instead, which cannot provide direct information about plant health. Moreover, equipment used for the direct monitoring of plant health are costly with complex operation, hindering their use by the wider community of farmers. This work reports for the first time the development of a flexible and highly transparent sensor, based on thin conductive PEDOT:PSS/PDMS hybrid films directly deposited onto leaves. The films were fabricated by aerosol deposition and could operate under two different modes. The first mode is used for the determination of plant dryness and concentration of ions. The second mode is used as a triboelectric generator to generate up to 7.2 µW cm⁻² electrical power through the friction of the sensors with a leaf. The device was assembled using a low-cost (GBP < 70) microcontroller incorporating environmental sensors, and an intuitive interface was designed for operation. The final sensor could determine the ionic strength at the millimolar level by means of the impedance of electrodes. This performance allowed the study of differences in ionic content and water availability in tomato leaves during day–night cycles. The high stability of the sensors also allowed the long-term monitoring of plant health. Using this technology, a decrease in the leaf ionic strength due to the lack of electrolytes was observed after watering with deionised water for 2 days. Upon supplementation with fertiliser, the recorded ionic strength and leaf water content were similar to the original values prior to the use of DI water, demonstrating the applicability of the device in the early detection of stress factors that could decrease crop production. Full article

(This article belongs to the Section Environmental Biosensors and Biosensing)

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19 pages, 2107 KB

Open AccessReview

Recent Advances in MXene-Based Screen-Printed Electrochemical Sensors for Point-of-Care Biomarker Detections

by Thao Thi Nguyen, Liang Zhou, Jinming Kong, Aiqin Luo, Zikai Hao and Jiangjiang Zhang

Biosensors 2025, 15(12), 804; https://doi.org/10.3390/bios15120804 - 8 Dec 2025

Viewed by 633

Abstract

Contemporary biomedical diagnostics increasingly demand high sensitivity for pathogen detection and real-time health monitoring. In response to these requirements, screen-printed electrochemical sensors (SPEs) have emerged as a practical analytical platform owing to their low cost, portability, and compatibility with point-of-care and wearable systems. [...] Read more.

Contemporary biomedical diagnostics increasingly demand high sensitivity for pathogen detection and real-time health monitoring. In response to these requirements, screen-printed electrochemical sensors (SPEs) have emerged as a practical analytical platform owing to their low cost, portability, and compatibility with point-of-care and wearable systems. In the recent past, nanomaterials in two-dimensional format, especially MXenes, have gained much interest due to their high electrical conductivity, controllable surface chemistry, and biocompatibility, which can improve the performance and applicability of SPEs. The current review concentrates on the latest developments between 2020 and 2025, providing a critical assessment of research employing MXene-based nanomaterials for the modification and development of screen-printed electrode platforms. We provide an overview of fabrication techniques, printing methods, and surface modification methods, and proceed with an analysis of the electrochemical performance of MXenes and MXene-based heterostructures. Lastly, contemporary issues are considered, and opinions are suggested to facilitate the translation of MXene-functionalized SPEs to real biomedical diagnosis solutions. Full article

(This article belongs to the Special Issue Point-of-Care Testing Using Biochemical Sensors for Health and Safety)

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13 pages, 3528 KB

Open AccessArticle

Urinary Metabolomic Changes and Potential Exercise-Induced Muscle Damage Biomarkers Identification in Trained Young Males Following Acute Intermittent Rowing Training

by Yang Cheng, Yue Yi, Xuefeng Shi and Shumin Bo

Biosensors 2025, 15(12), 803; https://doi.org/10.3390/bios15120803 - 8 Dec 2025

Viewed by 483

Abstract

(1) Background: This study aims to explore the changes in urinary metabolomic profile among trained young males following acute intermittent rowing training (AIRT), and to identify potential urinary biomarkers associated with exercise-induced muscle damage (EIMD). (2) Methods: 22 trained young males were recruited [...] Read more.

(1) Background: This study aims to explore the changes in urinary metabolomic profile among trained young males following acute intermittent rowing training (AIRT), and to identify potential urinary biomarkers associated with exercise-induced muscle damage (EIMD). (2) Methods: 22 trained young males were recruited to perform AIRT. The changes in blood biochemical indexes associated with EIMD were analyzed. EIMD occurrence was evaluated using blood biochemical indexes, muscle function, and pain assessment. The changes in urinary metabolites were determined using untargeted metabolomic analysis. (3) Results: Four blood biochemical indices, including creatine kinase, lactate dehydrogenase, creatine kinase-MB, and hydroxybutyrate dehydrogenase, were significantly elevated immediately after AIRT. Furthermore, an obvious immune response appeared, and countermovement jump performance significantly decreased. Among 384 urinary metabolites, 33 were significantly upregulated, and 12 were downregulated immediately after AIRT. Upregulated metabolites were mainly involved in phenylacetate metabolism, ammonia recycling, the urea cycle, and glutathione metabolism. Four potential urinary biomarkers were identified, including 2′-Deoxycytidine, cytosine, Phenylacetaldehyde, and Pyridoxamine. (4) Conclusions: AIRT induced EIMD in all participants and significantly altered urinary metabolite profiles. The changes in urinary metabolites and pathways were due to the metabolic adaptation to oxidative stress, inflammatory responses, and ammonia metabolism imbalance. The selected four potential urinary biomarkers provide important evidence for the further development of a non-invasive, urine-based method for the immediate assessment of EIMD. Full article

(This article belongs to the Special Issue Point-of-Care Testing Using Biochemical Sensors for Health and Safety)

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13 pages, 708 KB

Open AccessArticle

An Improved Dengue Virus Serotype-Specific Non-Structural Protein 1 Capture Immunochromatography Method with Reduced Sample Volume

by Warisara Sretapunya, Thitiya Buranachat, Montita Prasomthong, Rittichai Tantikorn, Areerat Sa-ngarsang, Sirirat Naemkhunthot, Laddawan Meephaendee, Pattara Wongjaroen, Chika Tanaka, Yoriko Shimadzu, Katsuya Ogata, Kunihiro Kaihatsu, Ryo Morita, Michinori Shirano, Juthamas Phadungsombat, Tadahiro Sasaki, Ritsuko Kubota-Koketsu, Yoshihiro Samune, Emi E. Nakayama and Tatsuo Shioda

Biosensors 2025, 15(12), 802; https://doi.org/10.3390/bios15120802 - 7 Dec 2025

Viewed by 454

Abstract

The four serotypes of dengue virus (DENV), types 1 to 4 (DENV-1 to DENV-4), exhibit approximately 60% identity in the encoded amino acid residues of viral proteins. Reverse transcription of RNA extracted from patient serum specimens followed by PCR amplification with serotype-specific probes [...] Read more.

The four serotypes of dengue virus (DENV), types 1 to 4 (DENV-1 to DENV-4), exhibit approximately 60% identity in the encoded amino acid residues of viral proteins. Reverse transcription of RNA extracted from patient serum specimens followed by PCR amplification with serotype-specific probes is the current standard technique for DENV serotyping. However, this method is time- and cost-consuming, and rapid detection systems with low cost are desirable. Previously, we developed a prototype serotype-specific immunochromatography system. That system was composed of four strips with four corresponding distinct sample buffers, each specifically detecting a single DENV serotype. In the present study, we improved this system by combining pairs of strips into one lateral-flow cassette each, providing DENV-1 and DENV-2 detection in one device and DENV-3 and DENV-4 detection in a second device; this strategy successfully reduced the required sample volume. Furthermore, we were able to adjust the composition of the sample buffers such that a single sample buffer sufficed for all four DENV serotype detection reactions, allowing much easier handling of the devices. Evaluation of this new device against laboratory and clinical DENV isolates and clinical specimens from DENV-infected individuals showed sensitivity that was comparable to that of our previous version, yielding serotype specificity of 100%. These new devices are expected to be of use in the clinical setting, accelerating both prospective and retrospective epidemiological studies. Full article

(This article belongs to the Special Issue Biosensors for Healthcare and Environment: Current and Future Perspectives)

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16 pages, 3740 KB

Open AccessArticle

The Role of Surfactants in Stabilizing Fluorescence Anisotropy for Protein–Aptamer Binding Affinity Measurements

by Bhagya R. Samarakoon, Susan L. Bilderback and Rebecca J. Whelan

Biosensors 2025, 15(12), 801; https://doi.org/10.3390/bios15120801 - 6 Dec 2025

Viewed by 408

Abstract

Fluorescence Anisotropy (FA) is a sensitive and efficient technique for quantifying biomolecular interactions, offering advantages such as minimal sample requirements and elimination of separation of bound from unbound species. Thus, it is well suited for aptamer–protein binding affinity studies. However, accurately determining equilibrium [...] Read more.

Fluorescence Anisotropy (FA) is a sensitive and efficient technique for quantifying biomolecular interactions, offering advantages such as minimal sample requirements and elimination of separation of bound from unbound species. Thus, it is well suited for aptamer–protein binding affinity studies. However, accurately determining equilibrium dissociation constants (K_D) in FA requires low concentrations of fluorescently labeled aptamers to prevent ligand depletion. A significant challenge arises at low aptamer concentrations due to an unexpected and physically nonmeaningful increase in apparent anisotropy, which impairs accurate data fitting. This anomalous increase in apparent anisotropy may arise from non-specific adsorption of aptamers to surfaces. In this study, we investigated the use of non-ionic surfactants to mitigate these effects and stabilize the anisotropy signal at low aptamer concentrations using the thrombin aptamer as a model system. We evaluated the impact of varying concentrations of two surfactants (Tween 20 and Triton X-100) on plots of anisotropy as a function of aptamer concentration and determined aptamer–protein binding affinities. Addition of 0.1% Tween 20 corrects the anomalous increase in anisotropy at low aptamer concentrations, enabling the use of aptamer concentrations as low as 5 nM in binding assays. Triton X-100 was less effective. By incorporating optimized concentrations of Tween 20, we demonstrated improved assay reproducibility and accuracy in K_D determination, expanding the dynamic range of usable aptamer concentrations in FA-based binding affinity studies. Similar benefits were observed with the clinically relevant aptamer s10yh2 and human serum albumin. These findings provide a practical strategy for enhancing the robustness of FA measurements and may be applicable to other aptamer–target systems and high-throughput assay formats. Full article

(This article belongs to the Special Issue Aptamer-Based Sensing: Designs and Applications)

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14 pages, 3378 KB

Open AccessArticle

Features of Chaperone Induction by 9-Aminoacridine and Acridine Orange

by Vadim V. Fomin, Svetlana V. Smirnova, Sergey V. Bazhenov, Aminat G. Kurkieva, Nikolay A. Bondarev, Daria M. Egorenkova, Daniil I. Sakharov, Ilya V. Manukhov and Serikbai K. Abilev

Biosensors 2025, 15(12), 800; https://doi.org/10.3390/bios15120800 - 6 Dec 2025

Viewed by 352

Abstract

The fluorescent dyes 9-aminoacridine (9-AA) and acridine orange (AO) are known mutagens that induce frameshift mutations in cells by intercalating between DNA bases. However, these chemicals can also affect other cellular components, such as proteins. In this study, we tested the ability of [...] Read more.

The fluorescent dyes 9-aminoacridine (9-AA) and acridine orange (AO) are known mutagens that induce frameshift mutations in cells by intercalating between DNA bases. However, these chemicals can also affect other cellular components, such as proteins. In this study, we tested the ability of 9-AA and AO to induce heat shock in bacteria using the following methods: lux-biosensors based on Escherichia coli cells with the luxCDABE genes transcriptionally fused to heat shock-specific inducible promoters, RT-qPCR, and nanoDSF. We demonstrated that acridine dyes not only induce mutagenesis but also cause heat shock in bacterial cells. AO significantly reduced the melting temperature of proteins and strongly activated σ^E- and σ³²-dependent promoters, but not PluxC, which is activated by elevated temperatures via a different mechanism. In contrast, 9-AA weakly denatured the proteins and induced the σ^E-dependent promoter; however, it activated the σ³²-dependent promoters and PluxC, supporting the hypothesis that the σ³² heat shock response system is activated via hairpin RNA denaturation by 9-AA. The study on the application of lux-biosensors was hampered by the high general toxicity and luminescence shielding effect of AO, and RT-qPCR’s sensitivity was insufficient for detection of the response to 9-AA. Thus, methodologically, it is justified to conduct a comprehensive study of substances that cause heat shock or affect bioluminescence by both RT-qPCR and lux-biosensors. Full article

(This article belongs to the Section Environmental Biosensors and Biosensing)

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34 pages, 3756 KB

Open AccessReview

Smart Nucleic Acid Hydrogel-Based Biosensors: From Molecular Recognition and Responsive Mechanisms to Applications

by Lu Xu, Longjiao Zhu, Xiaoyu Wang, Wenqiang Zhang, Xiaoyun He, Yangzi Zhang and Wentao Xu

Biosensors 2025, 15(12), 799; https://doi.org/10.3390/bios15120799 - 5 Dec 2025

Viewed by 738

Abstract

Smart nucleic acid hydrogels (SNAHs), endowed with stimulus responsiveness, function as programmable molecular switches that can perceive diverse external stimuli and undergo rapid, reversible, and highly specific conformational or performance changes. These dynamic properties have enabled the rational design of biosensors with bionic [...] Read more.

Smart nucleic acid hydrogels (SNAHs), endowed with stimulus responsiveness, function as programmable molecular switches that can perceive diverse external stimuli and undergo rapid, reversible, and highly specific conformational or performance changes. These dynamic properties have enabled the rational design of biosensors with bionic behaviors, facilitating cascaded “recognition–decision–execution” processes that support advanced biological analysis. Consequently, SNAHs are recognized as a core breakthrough for the next generation of intelligent biosensing units. However, a systematic mapping between SNAH design strategies, specific stimuli, and application fields remains lacking. This review mainly analyzes advances in SNAH-based biosensors over the past five years, proposing flexible and feasible design strategies and key trends in customization. Firstly, we systematically summarize molecular recognition modules involved in the construction of SNAHs, including aptamers, DNAzymes, antibodies, and specific binding peptides. Subsequently, we elaborate on the responses of these modules to external stimuli, so as to further facilitate the signal transduction of signals derived from physical, chemical, and biological sources involving temperature, light, magnetic fields, pH, nucleic acids, proteins, other biomolecules, and pathogens. Additionally, the review outlines the research progress of SNAHs in environmental monitoring, food safety, and medical diagnostics. Finally, we provide an integrated perspective on future opportunities and challenges, highlighting the innovative framework for designing SNAH-based biosensors and offering a practical roadmap for next-generation intelligent sensing applications. Full article

(This article belongs to the Special Issue Polymers-Based Biosensors and Bioelectronics: Designs and Applications)

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21 pages, 3571 KB

Open AccessArticle

Machine Learning-Based Toothbrushing Region Recognition Using Smart Toothbrush Holder and Wearable Sensors

by Hsuan-Chih Wang, Ju-Hsuan Li, Yen-Chen Lin, Che-Yu Lin, Chien-Pin Liu, Tzu-Han Lin, Chia-Tai Chan and Chia-Yeh Hsieh

Biosensors 2025, 15(12), 798; https://doi.org/10.3390/bios15120798 - 5 Dec 2025

Viewed by 438

Abstract

Oral health is a critical factor in maintaining overall health, and its association with systemic diseases, including cardiovascular disease and diabetes mellitus, has been extensively investigated. Effective plaque removal through proper toothbrushing techniques is fundamental for preventing dental caries and periodontal diseases. Despite [...] Read more.

Oral health is a critical factor in maintaining overall health, and its association with systemic diseases, including cardiovascular disease and diabetes mellitus, has been extensively investigated. Effective plaque removal through proper toothbrushing techniques is fundamental for preventing dental caries and periodontal diseases. Despite standardized guidelines, many individuals fail to adhere to correct brushing techniques, thereby increasing the risk of oral diseases. To address this issue, this study proposes a fine-grained toothbrushing region recognition approach incorporating six machine learning classifiers and two inertial measurement units (IMUs), which are embedded in the toothbrush holder and mounted on the right wrist of the participant, respectively. By analyzing the continuous motion signals, the proposed hierarchical approach is capable of identifying brushing and transition activities and subsequently recognizing specific toothbrushing regions based on the predicted brushing activities. To further improve recognition reliability, post-processing strategies such as contextual smoothing and majority voting are applied. Experimental results demonstrate that random forest achieves the highest recognition accuracy of 96.13%, sensitivity of 96.10%, precision of 95.51%, and F1-score of 95.60%. The results indicate that the proposed approach is both effective and feasible for providing fine-grained toothbrushing region recognition in toothbrushing monitoring. Full article

(This article belongs to the Special Issue Wearable Biosensors and Health Monitoring)

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26 pages, 2770 KB

Open AccessArticle

Cellular Distribution and Motion of Essential Magnetosome Proteins Expressed in Mammalian Cells

by Qin Sun, Cécile Fradin, Moeiz Ahmed, R. Terry Thompson, Frank S. Prato and Donna E. Goldhawk

Biosensors 2025, 15(12), 797; https://doi.org/10.3390/bios15120797 - 4 Dec 2025

Viewed by 382

Abstract

Magnetosomes are organelle-like structures within magnetotactic bacteria that store iron biominerals in membrane-bound vesicles. In bacteria, formation of these structures is highly regulated by approximately 30 genes, which are conserved throughout different species. To compartmentalize iron in mammalian cells and provide gene-based contrast [...] Read more.

Magnetosomes are organelle-like structures within magnetotactic bacteria that store iron biominerals in membrane-bound vesicles. In bacteria, formation of these structures is highly regulated by approximately 30 genes, which are conserved throughout different species. To compartmentalize iron in mammalian cells and provide gene-based contrast for magnetic resonance imaging, we introduced key magnetosome proteins. The expression of essential magnetosome genes mamI and mamL as fluorescent fusion proteins in a human melanoma cell line confirmed their co-localization and interaction. Here, we investigate the expression of two more essential magnetosome genes, mamB and mamE, using confocal microscopy to describe fluorescent fusion protein expression patterns and analyze the observed intracellular mobility. Custom software was developed to characterize fluorescent particle trajectories. In mammalian cells, essential magnetosome proteins display different diffusive behaviours. However, all magnetosome proteins travelled at similar velocities when interacting with mammalian mobile elements, suggesting that MamL, MamL + MamI, MamB, and MamE interact with similar molecular motor proteins. These results confirm that localization and interaction of essential magnetosome proteins are feasible within the mammalian intracellular compartment. Full article

(This article belongs to the Special Issue Fluorescent Probes: Design and Biological Applications)

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34 pages, 1737 KB

Open AccessReview

Digging into the Solubility Factor in Cancer Diagnosis: A Case of Soluble CD44 Protein

by Zhuldyz Myrkhiyeva, Marzhan Nurlankyzy, Kulzhan Berikkhanova, Zhanas Baimagambet, Aidana Bissen, Nurzhan Bikhanov, Christabel K. L. Tan, Daniele Tosi, Zhannat Ashikbayeva and Aliya Bekmurzayeva

Biosensors 2025, 15(12), 796; https://doi.org/10.3390/bios15120796 - 4 Dec 2025

Cited by 1 | Viewed by 480

Abstract

The detection of soluble proteins in biological fluids, as a form of liquid biopsy, is a promising tool for cancer diagnosis and prognosis, as it is less invasive than traditional diagnostic methods. CD44 is one of the most recognized markers of cancer stem [...] Read more.

The detection of soluble proteins in biological fluids, as a form of liquid biopsy, is a promising tool for cancer diagnosis and prognosis, as it is less invasive than traditional diagnostic methods. CD44 is one of the most recognized markers of cancer stem cells, a small subset of cells responsible for cancer initiation, progression, and metastasis. Given the importance of CD44 as a cancer biomarker, several review articles explore the diagnostic and therapeutic value of cell-surface CD44. In addition to being a membrane-anchored protein, CD44 is also shed from the cell surface and can be found in various biological fluids. However, the role of soluble CD44 in cancer has not been comprehensively discussed in recent reviews. Measuring soluble CD44 in various biological liquids can provide a practical and valuable tool for cancer diagnosis and treatment monitoring. Therefore, this review comprehensively discusses the role of soluble CD44 as a marker in various cancer types, including serum, saliva, urine, and other fluids. In particular, its role as an early cancer biomarker and as a predictive and prognostic biomarker in several cancers is discussed. This work also provides an overview of a wide range of analytical techniques used to detect soluble CD44. The value of cells expressing CD44 versus soluble CD44 as a biomarker is also compared. The review concludes with a perspective on future directions, emphasizing the shift toward non-invasive analytical methods and the need for standardization of detection, including multiple biomarkers during evaluation, to improve the accuracy of cancer diagnosis. Full article

(This article belongs to the Section Biosensors and Healthcare)

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15 pages, 2464 KB

Open AccessArticle

A Novel Approach for Tissue Analysis in Joint Infections Using the Scattered Light Integrating Collector (SLIC)

by Elio Assaf, Cosmea F. Amerschläger, Vincent B. Nessler, Kani Ali, Robert Ossendorff, Max Jaenisch, Andreas C. Strauss, Christof Burger, Gunnar T. Hischebeth, Phillip J. Walmsley, Dieter C. Wirtz, Robert J. H. Hammond, Damien Bertheloot and Frank A. Schildberg

Biosensors 2025, 15(12), 795; https://doi.org/10.3390/bios15120795 - 4 Dec 2025

Viewed by 386

Abstract

Total joint arthroplasty is among the most common surgical procedures performed worldwide, with frequency increasing due to demographic changes. Accelerating the diagnostic process using new techniques is crucial for effective therapy. This pilot study aims to test such innovative technology in the context [...] Read more.

Total joint arthroplasty is among the most common surgical procedures performed worldwide, with frequency increasing due to demographic changes. Accelerating the diagnostic process using new techniques is crucial for effective therapy. This pilot study aims to test such innovative technology in the context of periprosthetic joint infection (PJI) using Scattered Light Integrating Collector (SLIC) technology. While we wish to evaluate whether SLIC can be used to reliably detect the status of infection within human tissue samples in the future, our current research focused on building its foundation by evaluating steps of sample preparation that allow for heightened growth depiction. It is, to our knowledge, the first study concerning the usage of solid human tissue samples using the SLIC device. Adult patients presenting with native or periprosthetic joint infections were included in this prospective study. Biopsies were obtained using sequential sampling, and bacterial density was optimized through titration series. Cryopreservation and agents influencing coagulation were investigated. Our study demonstrates that simple pretreatment could aid in detecting pathogen growth in infected tissue samples. Findings showed a clear advantage for no addition of agents affecting coagulation. Additionally, our protocols proved reliable after prolonged cryopreservation at −20 °C for up to 8 weeks, showing no significant difference compared to primary testing. AUC comparison showed comparable results for sample storage at −80 °C for up to 8 weeks. Similar outcomes were seen for samples ranging from 25 µL to 300 µL, with biological replicates displaying higher thresholds for larger volumes without significant differences. This study introduces a simple and quick diagnostic tool for detecting bacterial growth using tissue biopsies and develops an SOP for further research with this innovative technique. The suggested SOP enables SLIC to hint at an underlying bacterial infection within 5 h using joint tissue, offering a possible novel approach in diagnosing periprosthetic joint infections and septic arthritis. While not yet designed to compare sensitivity to other culture methods, it provides a solid basis for further clinical research. Full article

(This article belongs to the Special Issue Sensors for Detection of Bacteria and Their Toxins)

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35 pages, 3387 KB

Open AccessReview

Immunosensing Platforms for Detection of Metabolic Biomarkers in Oral Fluids

by Nadezhda S. Komova, Kseniya V. Serebrennikova, Anatoly V. Zherdev and Boris B. Dzantiev

Biosensors 2025, 15(12), 794; https://doi.org/10.3390/bios15120794 - 2 Dec 2025

Viewed by 846

Abstract

Widespread and simple detection of diseases and disfunctions in the body is crucial for reliable and prompt diagnostics, efficient use of healthcare resources, and improved quality of life. The presence of a large number of metabolic products in saliva, the relationship between their [...] Read more.

Widespread and simple detection of diseases and disfunctions in the body is crucial for reliable and prompt diagnostics, efficient use of healthcare resources, and improved quality of life. The presence of a large number of metabolic products in saliva, the relationship between their levels in saliva and blood, the diagnostic value of many of these compounds, and the advantages of noninvasive sampling drive interest in oral fluid as a biomatrix. This review summarizes established oral fluid biomarkers, as well as potential salivary indicators for remote health monitoring and noninvasive point-of-care diagnostics. Recent advances in the search for new solutions for sensitive and high-throughput immunodetection of biomarkers in oral fluid are discussed, along with strategies for overcoming the analytical and technical challenges associated with the salivary matrix testing. Another focus of the current review is optical and electrochemical immunosensors with an emphasis on lateral flow immunoassays for point-of-care testing due to their speed, simplicity and cost-effectiveness. Finally, future directions are discussed that may enable non-invasive monitoring of endocrine, infectious, immune, neurodegenerative diseases and other human conditions using immunoassay platforms, paving the way for personalized and accessible healthcare. Full article

(This article belongs to the Special Issue Biosensing Technologies in Medical Diagnosis—2nd Edition)

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36 pages, 6926 KB

Open AccessReview

AI-Integrated Micro/Nanorobots for Biomedical Applications: Recent Advances in Design, Fabrication, and Functions

by Prashant Kishor Sharma and Chia-Yuan Chen

Biosensors 2025, 15(12), 793; https://doi.org/10.3390/bios15120793 - 2 Dec 2025

Viewed by 1525

Abstract

The integration of artificial intelligence (AI) and micro/nanorobotics is fundamentally reshaping biosensing by enabling autonomous, adaptive, and high-resolution biological analysis. These miniaturized robotic systems fabricated using advanced techniques such as photolithography, soft lithography, nanoimprinting, 3D printing, and self-assembly can navigate complex biological environments [...] Read more.

The integration of artificial intelligence (AI) and micro/nanorobotics is fundamentally reshaping biosensing by enabling autonomous, adaptive, and high-resolution biological analysis. These miniaturized robotic systems fabricated using advanced techniques such as photolithography, soft lithography, nanoimprinting, 3D printing, and self-assembly can navigate complex biological environments to perform targeted sensing, diagnostics, and therapeutic delivery. AI-driven algorithms, mainly those in machine learning (ML) and deep learning (DL), act as the brains of the operation, allowing for sophisticated modeling, genuine real-time control, and complex signal interpretation. This review focuses recent advances in the design, fabrication, and functional integration of AI-enabled micro/nanorobots for biomedical sensing. Applications that demonstrate their potential range from quick point-of-care diagnostics and in vivo biosensing to next-generation organ-on-chip systems and truly personalized medicine. We also discuss key challenges in scalability, energy autonomy, data standardization, and closed-loop control. Collectively, these advancements are paving the way for intelligent, responsive, and clinically transformative biosensing systems. Full article

(This article belongs to the Section Biosensors and Healthcare)

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