Polymers-Based Biosensors and Bioelectronics: Designs and Applications

A special issue of Biosensors (ISSN 2079-6374). This special issue belongs to the section "Biosensor Materials".

Deadline for manuscript submissions: 30 March 2026 | Viewed by 15703

Special Issue Editor


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Guest Editor
Laser and Thermal Engineering Laboratory, Department of Mechanical Engineering, Gachon University, Seongnam 13120, Republic of Korea
Interests: biosensors; chemical sensors; hydrogels; organic field-effect transistors; conjugated polymers; photo-catalyts
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Special Issue Information

Dear Colleagues,

Following the success of the first volume of the Special Issue entitled "Conjugated Polymers-Based Biosensors for Virus Detection", we are pleased to announce a new edition, entitled "Polymers-Based Biosensors and Bioelectronics: Designs and Applications". This Special Issue will continue to explore the innovative use of polymer materials in the development of biosensors and bioelectronic devices.

As the need for sensitive and selective detection methods grows in fields such as healthcare, environmental monitoring, and food safety, polymers have become indispensable materials. Their unique properties—such as flexibility, biocompatibility, and ease of functionalization—make them highly suitable for these applications.

This Special Issue will focus on recent advancements in the design, fabrication, and application of polymer-based biosensors and bioelectronic systems. We welcome the submission of original research articles, reviews, and short communications addressing a range of topics, including novel polymeric materials, integration techniques, sensing mechanisms, and practical applications in diagnostics and monitoring.

By gathering diverse contributions from researchers and industry experts, we aim to foster collaboration and knowledge exchange in this rapidly evolving field. We believe that this Special Issue will be a valuable resource for scientists and engineers working at the intersection of polymer science, biosensing technology, and bioelectronics, ultimately contributing to the advancement of next-generation sensing solutions.

Dr. Vinh Van Tran
Guest Editor

Manuscript Submission Information

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Keywords

  • polymers-based biosensor
  • gas sensor
  • transistor-based biosensor
  • organic field-effect transistors (OFETs)
  • conductive polymers
  • organic electronics
  • smart materials (self-healable materials, hydrogels)

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Published Papers (7 papers)

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Research

Jump to: Review

14 pages, 7832 KB  
Article
Self-Adaptive Polymer Fabry–Pérot Thermometer for High-Sensitivity and Wide-Linear-Range Sensing
by Yifan Cheng, Maolin Yu, Junjie Liu, Yingling Tan and Jinhui Chen
Biosensors 2025, 15(9), 602; https://doi.org/10.3390/bios15090602 - 12 Sep 2025
Viewed by 489
Abstract
Fiber-optic temperature sensors with advantages such as simplicity, low cost, and high sensitivity have attracted increasing attention. In this work, we propose a self-adaptive polymer Fabry–Pérot interferometer (PFPI) sensor for ultrasensitive and wide-linear-range thermal sensing. This design achieves a temperature sensitivity of 0.95 [...] Read more.
Fiber-optic temperature sensors with advantages such as simplicity, low cost, and high sensitivity have attracted increasing attention. In this work, we propose a self-adaptive polymer Fabry–Pérot interferometer (PFPI) sensor for ultrasensitive and wide-linear-range thermal sensing. This design achieves a temperature sensitivity of 0.95 nm/°C, representing an enhancement of two orders of magnitude compared to conventional fiber Bragg gratings. To address the challenge of spectral shifts exceeding the free spectral range due to the high sensitivity, a local cross-correlation algorithm is introduced for accurate wavelength tracking. We demonstrate ultrahigh-resolution (0.025 °C) scanning thermal field imaging and sensitive human physiological monitoring, including precise body temperature and respiratory rate detection. These results highlight the dual capability of our PFPI sensor for both microscopic thermal mapping and non-invasive healthcare applications. Full article
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22 pages, 2504 KB  
Article
Fluorogenic Biosensing with Tunable Polydiacetylene Vesicles
by John S. Miller, Tanner J. Finney, Ethan Ilagan, Skye Frank, Ye Chen-Izu, Keishi Suga and Tonya L. Kuhl
Biosensors 2025, 15(1), 27; https://doi.org/10.3390/bios15010027 - 7 Jan 2025
Cited by 1 | Viewed by 1747
Abstract
Polydiacetylenes (PDAs) are conjugated polymers that are well known for their colorimetric transition from blue to red with the application of energetic stimulus. Sensing platforms based on polymerized diacetylene surfactant vesicles and other structures have been widely demonstrated for various colorimetric biosensing applications. [...] Read more.
Polydiacetylenes (PDAs) are conjugated polymers that are well known for their colorimetric transition from blue to red with the application of energetic stimulus. Sensing platforms based on polymerized diacetylene surfactant vesicles and other structures have been widely demonstrated for various colorimetric biosensing applications. Although less studied and utilized, the transition also results in a change from a non-fluorescent to a highly fluorescent state, making polydiacetylenes useful for both colorimetric and fluorogenic sensing applications. Here, we focus on the characterization and optimization of polydiacetylene vesicles to tune their sensitivity for fluorogenic sensing applications. Particularly, we look at how the structure of the diacetylene (DA) hydrocarbon tail and headgroup affect the self-assembled vesicle size and stability, polymerization kinetics, and the fluorogenic, blue to red phase transition. Longer DA acyl tails generally resulted in smaller and more stable vesicles. The polymerization kinetics and the blue to red transition were a function of both the DA acyl tail length and structure of the headgroup. Decreasing the acyl tail length generally led to vesicles that were more sensitive to energetic stimuli. Headgroup modifications had different effects depending on the structure of the headgroup. Ethanolamine headgroups resulted in vesicles with potentially increased stimuli responsivity. The lower energy stimulus to induce the chromatic transition was attributed to an increase in headgroup hydrogen bonding and polymer backbone strain. Boronic-acid headgroup functionalization led to vesicles that were generally unstable, only weakly polymerized, and unable to fully transform to the red phase due to strong polar, aromatic headgroup interactions. This work presents the design of PDA vesicles in the context of biosensing platforms and includes a discussion of the past, present, and future of PDA biosensing. Full article
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12 pages, 4552 KB  
Article
Concave Magnetic-Responsive Hydrogel Discs for Enhanced Bioassays
by Amin Ghaffarzadeh Bakhshayesh and Huiyan Li
Biosensors 2024, 14(12), 596; https://doi.org/10.3390/bios14120596 - 5 Dec 2024
Cited by 2 | Viewed by 1514
Abstract
Receptor-based biosensors often suffer from slow analyte diffusion, leading to extended assay times. Moreover, existing methods to enhance diffusion can be complex and costly. In response to this challenge, we presented a rapid and cost-effective technique for fabricating concave magnetic-responsive hydrogel discs (CMDs) [...] Read more.
Receptor-based biosensors often suffer from slow analyte diffusion, leading to extended assay times. Moreover, existing methods to enhance diffusion can be complex and costly. In response to this challenge, we presented a rapid and cost-effective technique for fabricating concave magnetic-responsive hydrogel discs (CMDs) by straightforward pipetting directly onto microscope glass slides. This approach enables immediate preparation and customization of hydrogel properties such as porosity, magnetic responsiveness, and embedded particles and is adaptable for use with microarray printers. The concave design increased the surface area by 43% compared to conventional hemispherical hydrogels, enhancing diffusion rates and accelerating reactions. By incorporating superparamagnetic particles, the hydrogels become magnetically responsive, allowing for stirring within reagent droplets using magnets to improve mixing. Our experimental results showed that CMDs dissolved approximately 2.5 times faster than hemispherical ones. Numerical simulations demonstrated up to a 46% improvement in diffusion speed within the hydrogel. Particles with lower diffusion coefficients, like human antibodies, benefited most from the concave design, resulting in faster biosensor responses. The increased surface area and ease of fabrication make our CMDs efficient and adaptable for various biological and biomedical applications, particularly in point-of-care diagnostics where rapid and accurate biomarker detection is critical. Full article
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Review

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47 pages, 15990 KB  
Review
Single-Molecule Detection Technologies: Advances in Devices, Transduction Mechanisms, and Functional Materials for Real-World Biomedical and Environmental Applications
by Sampa Manoranjan Barman, Arpita Parakh, A. Anny Leema, P. Balakrishnan, Ankita Avthankar, Dhiraj P. Tulaskar, Purshottam J. Assudani, Shon Nemane, Prakash Rewatkar, Madhusudan B. Kulkarni and Manish Bhaiyya
Biosensors 2025, 15(10), 696; https://doi.org/10.3390/bios15100696 - 14 Oct 2025
Viewed by 752
Abstract
Single-molecule detection (SMD) has reformed analytical science by enabling the direct observation of individual molecular events, thus overcoming the limitations of ensemble-averaged measurements. This review presents a comprehensive analysis of the principles, devices, and emerging materials that have shaped the current landscape of [...] Read more.
Single-molecule detection (SMD) has reformed analytical science by enabling the direct observation of individual molecular events, thus overcoming the limitations of ensemble-averaged measurements. This review presents a comprehensive analysis of the principles, devices, and emerging materials that have shaped the current landscape of SMD. We explore a wide range of sensing mechanisms, including surface plasmon resonance, mechanochemical transduction, transistor-based sensing, optical microfiber platforms, fluorescence-based techniques, Raman scattering, and recognition tunneling, which offer distinct advantages in terms of label-free operation, ultrasensitivity, and real-time responsiveness. Each technique is critically examined through representative case studies, revealing how innovations in device architecture and signal amplification strategies have collectively pushed the detection limits into the femtomolar to attomolar range. Beyond the sensing principles, this review highlights the transformative role of advanced nanomaterials such as graphene, carbon nanotubes, quantum dots, MnO2 nanosheets, upconversion nanocrystals, and magnetic nanoparticles. These materials enable new transduction pathways and augment the signal strength, specificity, and integration into compact and wearable biosensing platforms. We also detail the multifaceted applications of SMD across biomedical diagnostics, environmental monitoring, food safety, neuroscience, materials science, and quantum technologies, underscoring its relevance to global health, safety, and sustainability. Despite significant progress, the field faces several critical challenges, including signal reproducibility, biocompatibility, fabrication scalability, and data interpretation complexity. To address these barriers, we propose future research directions involving multimodal transduction, AI-assisted signal analytics, surface passivation techniques, and modular system design for field-deployable diagnostics. By providing a cross-disciplinary synthesis of device physics, materials science, and real-world applications, this review offers a comprehensive roadmap for the next generation of SMD technologies, poised to impact both fundamental research and translational healthcare. Full article
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32 pages, 5916 KB  
Review
Advances and Innovations in Conjugated Polymer Fluorescent Sensors for Environmental and Biological Detection
by Viet-Duc Phung and Vinh Van Tran
Biosensors 2025, 15(9), 580; https://doi.org/10.3390/bios15090580 - 4 Sep 2025
Viewed by 1173
Abstract
Thanks to their multiple outstanding features—such as high fluorescence quantum yield, good photostability, and excellent sensitivity—conjugated polymers (CPs) have emerged as a pioneering class of fluorescent materials for sensing applications, particularly in environmental and biological fields, for the detection of a wide range [...] Read more.
Thanks to their multiple outstanding features—such as high fluorescence quantum yield, good photostability, and excellent sensitivity—conjugated polymers (CPs) have emerged as a pioneering class of fluorescent materials for sensing applications, particularly in environmental and biological fields, for the detection of a wide range of environmental pollutants and bioactive compounds. The presence of delocalized π-electrons in the CP backbone significantly enhances sensing performance through a unique phenomenon known as the “molecular wire effect.” As a result, CP-based fluorescent sensors have been extensively developed and employed as exceptional tools for monitoring various analytes in environmental and biological contexts. A deep understanding of their unique properties, fabrication techniques, and recent innovations is essential for guiding the strategic development of advanced CP-based fluorescent sensors, particularly for future point-of-care applications. This study presents a critical review of the key characteristics of fluorescent sensors and highlights several common types of conjugated polymers (CPs) used in their design and fabrication. It summarizes and discusses the main sensing mechanisms, state-of-the-art applications, and recent innovations of CP-based fluorescent sensors for detecting target compounds in environmental and biological fields. Furthermore, potential strategies and future perspectives for designing and developing high-performance CP-based fluorescent sensors are emphasized. By consolidating current scientific evidence, this review aims to support the advancement of highly sensitive fluorescent sensors based on various CP nanoparticles for environmental and biological applications. Full article
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19 pages, 5119 KB  
Review
Carbon Quantum Dots: Synthesis, Characteristics, and Quenching as Biocompatible Fluorescent Probes
by Arif Kamal, Seongin Hong and Heongkyu Ju
Biosensors 2025, 15(2), 99; https://doi.org/10.3390/bios15020099 - 10 Feb 2025
Cited by 17 | Viewed by 5546
Abstract
Carbon quantum dots (CQDs), a new class of carbon-based nanomaterials, have emerged as nano-scaled probes with photoluminescence that have an eco-friendly and bio-compatible nature. Their cost-efficient synthesis and high photoluminescence quantum yields make them indispensable due to their application in opto-electronic devices, including [...] Read more.
Carbon quantum dots (CQDs), a new class of carbon-based nanomaterials, have emerged as nano-scaled probes with photoluminescence that have an eco-friendly and bio-compatible nature. Their cost-efficient synthesis and high photoluminescence quantum yields make them indispensable due to their application in opto-electronic devices, including biosensors, bioimaging, environmental monitoring, and light sources. This review provides intrinsic properties of CQDs such as their excitation-dependent emission, biocompatibility, and quenching properties. Diverse strategies for their easy synthesis are divided into bottom-up and top-down approaches and detailed herein. In particular, we highlight their luminescence properties, including quenching mechanisms that could even be utilized for the precise and rapid detection of biomolecules. We also discuss methodologies for the mitigation of fluorescence quenching, which is pivotal for the application of CQDs in biosensors and bioimaging. Full article
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25 pages, 3691 KB  
Review
Metal–Organic Framework-Based Nanostructures for Electrochemical Sensing of Sweat Biomarkers
by Jing Meng, Moustafa Zahran and Xiaolin Li
Biosensors 2024, 14(10), 495; https://doi.org/10.3390/bios14100495 - 12 Oct 2024
Cited by 9 | Viewed by 3530
Abstract
Sweat is considered the most promising candidate to replace conventional blood samples for noninvasive sensing. There are many tools and optical and electrochemical methods that can be used for detecting sweat biomarkers. Electrochemical methods are known for their simplicity and cost-effectiveness. However, they [...] Read more.
Sweat is considered the most promising candidate to replace conventional blood samples for noninvasive sensing. There are many tools and optical and electrochemical methods that can be used for detecting sweat biomarkers. Electrochemical methods are known for their simplicity and cost-effectiveness. However, they need to be optimized in terms of selectivity and catalytic activity. Therefore, electrode modifiers such as nanostructures and metal–organic frameworks (MOFs) or combinations of them were examined for boosting the performance of the electrochemical sensors. The MOF structures can be prepared by hydrothermal/solvothermal, sonochemical, microwave synthesis, mechanochemical, and electrochemical methods. Additionally, MOF nanostructures can be prepared by controlling the synthesis conditions or mixing bulk MOFs with nanoparticles (NPs). In this review, we spotlight the previously examined MOF-based nanostructures as well as promising ones for the electrochemical determination of sweat biomarkers. The presence of NPs strongly improves the electrical conductivity of MOF structures, which are known for their poor conductivity. Specifically, Cu-MOF and Co-MOF nanostructures were used for detecting sweat biomarkers with the lowest detection limits. Different electrochemical methods, such as amperometric, voltammetric, and photoelectrochemical, were used for monitoring the signal of sweat biomarkers. Overall, these materials are brilliant electrode modifiers for the determination of sweat biomarkers. Full article
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