Applications of Advanced Electrochemical (Bio)sensors in Environment, Food, and Medicine

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

Deadline for manuscript submissions: 30 April 2025 | Viewed by 16201

Special Issue Editors


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Guest Editor
Institute of Botany, Jiangsu Province and Chinese Academy of Sciences, Nanjing 210014, China
Interests: the application of electrochemical and (bio)sensors in plants

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Guest Editor
School of Applied Sciences, University of the West of England, Bristol BS16 1QY, UK
Interests: screen printed electrode; sensor for health technology application; point of care instrument, environmental, and nanotechnology applications
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Special Issue Information

Dear Colleagues,

The environment, food and medicine are the three major fields most closely related to people's daily lives. With a population increasing and the pressures of economic development, there are more and more challenges facing these three fields; such as population growth; exerting pressure on environment quality, food production and the spread of diseases. Economic development has led to improved living conditions and stimulated demand for better food safety and health. Hence, sensor technology focused on environment protection, food quality control and medicine have become research hotspots. Electrochemical sensors and biosensors have been widely used in these three fields due to their excellent selectivity and sensitivity. They are small and portable, allowing them to be widely applied in both static and mobile platforms and for the possibility of use in the field, at the point-of-need.

This Special Issue is focused on the applications of advanced electrochemical (bio)sensors in fields of the environment, food, and medicine. It aims to provide a platform for the publication of original high-quality research papers covering the most recent advances in these areas, as well as comprehensive reviews on the application of both the electrochemical and non-electrochemical sensing and bio-sensing technologies in these fields. We invited a wide range of appropriate contributions and should covers any type of experimental, theoretical, numerical, and computational research in the areas of both electrochemical and non-electrochemical (bio) sensors in for environment, food, and medicine. This includes (but is not limited to) theoretical development, mathematical models, numerical algorithms, optimization, machine learning approaches, probabilistic and stochastic approaches, and computational methods. Discussions of electrochemical and nonelectrochemical sensors employing both classical and advanced techniques, based on enzymes, antibodies, DNA, aptamers, molecularly imprinted polymers, and the application of nanotechnology are also welcome.

Dr. Kevin C. Honeychurch
Dr. Yuhong Zheng
Dr. Martina Piano
Guest Editors

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Keywords

  • electrochemical sensors
  • biosensors
  • food safety
  • food quality control
  • enviromental pollution monitoring
  • medicine
  • detection
  • analysis

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Published Papers (8 papers)

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Research

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12 pages, 5945 KiB  
Article
Sea Urchin-like Magnetic Microbeads-Based Electrochemical Biosensor for Highly Sensitive Detection of Metabolites
by Bin Chen, Xiaosu Yuan, Enze Tian, Yunjie Tan, Le Li and Ru Huang
Biosensors 2025, 15(4), 225; https://doi.org/10.3390/bios15040225 - 2 Apr 2025
Viewed by 228
Abstract
Analyzing metabolite levels in bodily fluids is essential for disease diagnosis and surveillance. Electrochemical biosensors are ideal for monitoring metabolite levels due to their high sensitivity, rapid response, and low cost. The magnetic microbeads-based electrode functionalization method further promotes the automation development of [...] Read more.
Analyzing metabolite levels in bodily fluids is essential for disease diagnosis and surveillance. Electrochemical biosensors are ideal for monitoring metabolite levels due to their high sensitivity, rapid response, and low cost. The magnetic microbeads-based electrode functionalization method further promotes the automation development of electrochemical biosensors by eliminating the tedious electrode polishing process. In this study, we presented sea urchin-like magnetic microbeads (SMMBs) and constructed an SMMB-based electrochemical biosensor. The specific morphology of SMMBs provides a larger specific surface area and abundant enzyme binding sites, thereby expanding the active reaction interface on the electrode and improving the sensitivity of the biosensor. Experiment results demonstrated that the SMMB-based electrochemical biosensor achieves μM level detection sensitivity for glucose. Furthermore, by replacing the anchored oxidase on SMMBs, the biosensor can be extended to detect other metabolites, such as cholesterol. In summary, the SMMBs provide a new path to handily construct electrochemical biosensors and hold a great potential for metabolite detection and further development. Full article
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21 pages, 3054 KiB  
Article
Curcumin Electroanalysis at a Disposable Graphite Electrode
by Mihaela-Carmen Cheregi, Alina Tirsoaga, Cosmina Ion, Emilia-Elena Iorgulescu, Iulia Gabriela David and Hassan Noor
Biosensors 2025, 15(3), 137; https://doi.org/10.3390/bios15030137 - 23 Feb 2025
Viewed by 779
Abstract
Curcumin (CU, turmeric), a polyphenolic phytochemical that is largely used as a food spice, has benefits for human health, which have led to increased interest in its therapeutic applications and its analysis from different matrices. The two guaiacol moieties of CU are responsible [...] Read more.
Curcumin (CU, turmeric), a polyphenolic phytochemical that is largely used as a food spice, has benefits for human health, which have led to increased interest in its therapeutic applications and its analysis from different matrices. The two guaiacol moieties of CU are responsible for its antioxidant properties and allow for its voltammetric quantification. Cyclic and differential pulse voltammetry (DPV) investigations at a single-use pencil graphite electrode (PGE) emphasized complex pH-dependent electrode processes, involving an equal number of protons and electrons. Theoretical calculations predicted a folded geometry for the β-diketone CU conformers, which interact with the PGE surface, exposing the electroactive moieties of only one aromatic ring. The Gibbs energy variations of the structures involved in CU electro-oxidation and the theoretical electrochemical potential values were calculated. CU’s DPV cathodic peak intensity recorded at an HB-type PGE in 0.05 mol × L−1 H2SO4 varied linearly in the range 5.00 × 10−8–5.00 × 10−6 mol × L−1 CU. The method’s detection and quantification limits were 2.12 × 10−8 mol × L−1 and 6.42 × 10−8 mol × L−1, respectively. The practical applicability of the developed method, successfully tested by CU assessment in dietary supplements, provided a recovery of 99.28 ± 2.04%. Full article
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17 pages, 3676 KiB  
Article
Electrochemical Determination of Doxorubicin in the Presence of Dacarbazine Using MWCNTs/ZnO Nanocomposite Modified Disposable Screen-Printed Electrode
by Somayeh Tajik, Hadi Beitollahi, Fariba Garkani Nejad and Zahra Dourandish
Biosensors 2025, 15(1), 60; https://doi.org/10.3390/bios15010060 - 17 Jan 2025
Viewed by 1044
Abstract
In the current work, the MWCNTs/ZnO nanocomposite was successfully synthesized using simple method. Then, FE-SEM, XRD, and EDX techniques were applied for morphological and structural characterization. Afterward, a sensitive voltammetric sensor based on modification of a screen-printed carbon electrode (SPCE) using MWCNTs/ZnO nanocomposite [...] Read more.
In the current work, the MWCNTs/ZnO nanocomposite was successfully synthesized using simple method. Then, FE-SEM, XRD, and EDX techniques were applied for morphological and structural characterization. Afterward, a sensitive voltammetric sensor based on modification of a screen-printed carbon electrode (SPCE) using MWCNTs/ZnO nanocomposite was developed for the determination of doxorubicin in the presence of dacarbazine. To evaluate the electrochemical response of the MWCNTs/ZnO/SPCE towards doxorubicin, cyclic voltammetry (CV) was applied. The MWCNTs/ZnO nanocomposite showed a significant synergistic effect on the electrochemical response of the electrode for the redox reaction of doxorubicin. Also, the MWCNTs/ZnO/SPCE demonstrated an enhanced sensing platform for the quantification of doxorubicin, obtaining a detection limit (LOD) of 0.002 µM and a sensitivity of 0.0897 µA/µM, as determined by differential pulse voltammetry (DPV) within a linear range from 0.007 to 150.0 µM. Also, the MWCNTs/ZnO nanocomposite-modified SPCE showed high electrochemical activities towards the oxidation of doxorubicin and dacarbazine with peak-potential separation of 345 mV, which is sufficient for doxorubicin determination in the presence of dacarbazine. Also, the MWCNTs/ZnO nanocomposite-modified SPCE presented reproducible and stable responses to determine doxorubicin. Finally, the developed platform demonstrated a successful performance for doxorubicin and dacarbazine determination in real samples, with recovery in the range of 97.1% to 104.0% and relative standard deviation (RSD) from 1.8% to 3.5%. Full article
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14 pages, 4281 KiB  
Article
Enhancing Heavy Metal Detection through Electrochemical Polishing of Carbon Electrodes
by Sanjeev Billa, Rohit Boddu, Shabnam Siddiqui and Prabhu U. Arumugam
Biosensors 2024, 14(9), 412; https://doi.org/10.3390/bios14090412 - 24 Aug 2024
Cited by 1 | Viewed by 1875
Abstract
Our research addresses the pressing need for environmental sensors capable of large-scale, on-site detection of a wide array of heavy metals with highly accurate sensor metrics. We present a novel approach using electrochemically polished (ECP) carbon screen-printed electrodes (cSPEs) for high-sensitivity detection of [...] Read more.
Our research addresses the pressing need for environmental sensors capable of large-scale, on-site detection of a wide array of heavy metals with highly accurate sensor metrics. We present a novel approach using electrochemically polished (ECP) carbon screen-printed electrodes (cSPEs) for high-sensitivity detection of cadmium and lead. By applying a range of techniques, including scanning electron microscopy, energy-dispersive spectroscopy, Raman spectroscopy, electrochemical impedance spectroscopy, and cyclic voltammetry, we investigated the impact of the electrochemical potential scan range, scan rate, and the number of cycles on electrode response and its ability to detect cadmium and lead. Our findings reveal a 41 ± 1.2% increase in voltammogram currents and a 51 ± 1.6% decrease in potential separations (n = 3), indicating a significantly improved active electrode area and kinetics. The impedance model elucidates the microstructural and electrochemical property changes in the ECP-treated electrodes, showing an 88 ± 2% (n = 3) decrease in the charge transfer resistance, leading to enhanced electrode electrical conductivity. A bismuth-reduced graphene oxide nanocomposite-modified, ECP-treated electrode demonstrated a higher cadmium and lead sensitivity of up to 5 ± 0.1 μAppb−1cm−2 and 2.7 ± 0.1 μAppb−1cm−2 (n = 3), respectively, resulting in sub-ppb limits of detection in spiked deionized water samples. Our study underscores the potential of optimally ECP-activated electrodes as a foundation for designing ultrasensitive heavy metal sensors for a wide range of real-world heavy metal-contaminated waters. Full article
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12 pages, 2040 KiB  
Article
Electrochemical Aptasensing Platform for the Detection of Retinol Binding Protein-4
by Kamila Malecka-Baturo, Paulina Żółtowska, Agnieszka Jackowska, Katarzyna Kurzątkowska-Adaszyńska and Iwona Grabowska
Biosensors 2024, 14(2), 101; https://doi.org/10.3390/bios14020101 - 16 Feb 2024
Cited by 2 | Viewed by 2972
Abstract
Here, we present the results of our the electrochemical aptasensing strategy for retinol binding protein-4 (RBP-4) detection based on a thiolated aptamer against RBP-4 and 6-mercaptohexanol (MCH) directly immobilized on a gold electrode surface. The most important parameters affecting the magnitude of the [...] Read more.
Here, we present the results of our the electrochemical aptasensing strategy for retinol binding protein-4 (RBP-4) detection based on a thiolated aptamer against RBP-4 and 6-mercaptohexanol (MCH) directly immobilized on a gold electrode surface. The most important parameters affecting the magnitude of the analytical signal generated were optimized: (i) the presence of magnesium ions in the immobilization and measurement buffer, (ii) the concentration of aptamer in the immobilization solution and (iii) its folding procedure. In this work, a systematic assessment of the electrochemical parameters related to the optimization of the sensing layer of the aptasensor was carried out (electron transfer coefficients (α), electron transfer rate constants (k0) and surface coverage of the thiolated aptamer probe (ΓApt)). Then, under the optimized conditions, the analytical response towards RBP-4 protein, in the presence of an Fe(CN)63−/4− redox couple in the supporting solution was assessed. The proposed electrochemical strategy allowed for RBP-4 detection in the concentration range between 100 and 1000 ng/mL with a limit of detection equal to 44 ng/mL based on electrochemical impedance spectroscopy (EIS). The specificity studies against other diabetes biomarkers, including vaspin and adiponectin, proved the selectivity of the proposed platform. These preliminary results will be used in the next step to miniaturize and test the sensor in real samples. Full article
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13 pages, 1496 KiB  
Article
Development of Taste Sensor with Lipid/Polymer Membranes for Detection of Umami Substances Using Surface Modification
by Wenhao Yuan, Zeyu Zhao, Shunsuke Kimura and Kiyoshi Toko
Biosensors 2024, 14(2), 95; https://doi.org/10.3390/bios14020095 - 11 Feb 2024
Cited by 3 | Viewed by 2629
Abstract
A taste sensor employs various lipid/polymer membranes with specific physicochemical properties for taste classification and evaluation. However, phosphoric acid di(2-ethylhexyl) ester (PAEE), employed as one of the lipids for the taste sensors, exhibits insufficient selectivity for umami substances. The pH of sample solutions [...] Read more.
A taste sensor employs various lipid/polymer membranes with specific physicochemical properties for taste classification and evaluation. However, phosphoric acid di(2-ethylhexyl) ester (PAEE), employed as one of the lipids for the taste sensors, exhibits insufficient selectivity for umami substances. The pH of sample solutions impacts the dissociation of lipids to influence the membrane potential, and the response to astringent substances makes accurate measurement of umami taste difficult. This study aims to develop a novel taste sensor for detecting umami substances like monosodium L-glutamate (MSG) through surface modification, i.e., a methodology previously applied to taste sensors for non-charged bitter substance measurement. Four kinds of modifiers were tested as membrane-modifying materials. By comparing the results obtained from these modifiers, the modifier structure suitable for measuring umami substances was identified. The findings revealed that the presence of carboxyl groups at para-position of the benzene ring, as well as intramolecular H-bonds between the carboxyl group and hydroxyl group, significantly affect the effectiveness of a modifier in the umami substance measurement. The taste sensor treated with this type of modifier showed excellent selectivity for umami substances. Full article
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17 pages, 5352 KiB  
Article
An Electrochemical Screen-Printed Sensor Based on Gold-Nanoparticle-Decorated Reduced Graphene Oxide–Carbon Nanotubes Composites for the Determination of 17-β Estradiol
by Auwal M. Musa, Janice Kiely, Richard Luxton and Kevin C. Honeychurch
Biosensors 2023, 13(4), 491; https://doi.org/10.3390/bios13040491 - 19 Apr 2023
Cited by 23 | Viewed by 4648 | Correction
Abstract
In this study, a screen-printed electrode (SPE) modified with gold-nanoparticle-decorated reduced graphene oxide–carbon nanotubes (rGO-AuNPs/CNT/SPE) was used for the determination of estradiol (E2). The AuNPs were produced through an eco-friendly method utilising plant extract, eliminating the need for severe chemicals, and remove the [...] Read more.
In this study, a screen-printed electrode (SPE) modified with gold-nanoparticle-decorated reduced graphene oxide–carbon nanotubes (rGO-AuNPs/CNT/SPE) was used for the determination of estradiol (E2). The AuNPs were produced through an eco-friendly method utilising plant extract, eliminating the need for severe chemicals, and remove the requirements of sophisticated fabrication methods and tedious procedures. In addition, rGO-AuNP serves as a dispersant for the CNT to improve the dispersion stability of CNTs. The composite material, rGO-AuNPs/CNT, underwent characterisation through scanning electron microscopy (SEM), ultraviolet–visible absorption spectroscopy (UV–vis), Fourier-transform infrared (FTIR) spectroscopy, and atomic force microscopy (AFM). The electrochemical performance of the modified SPE for estradiol oxidation was characterised using cyclic voltammetry (CV) and differential pulse voltammetry (DPV) techniques. The rGO-AuNPs/CNT/SPE exhibited a notable improvement compared to bare/SPE and GO-CNT/SPE, as evidenced by the relative peak currents. Additionally, we employed a baseline correction algorithm to accurately adjust the sensor response while eliminating extraneous background components that are typically present in voltammetric experiments. The optimised estradiol sensor offers linear sensitivity from 0.05–1.00 µM, with a detection limit of 3 nM based on three times the standard deviation (3δ). Notably, this sensing approach yields stable, repeatable, and reproducible outcomes. Assessment of drinking water samples indicated an average recovery rate of 97.5% for samples enriched with E2 at concentrations as low as 0.5 µM%, accompanied by only a modest coefficient of variation (%CV) value of 2.7%. Full article
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Review

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32 pages, 4902 KiB  
Review
Aspects of Electrochemical Biosensors Using Affinity Assays
by Thor Pedersen, Leonid Gurevich and Nils E. Magnusson
Biosensors 2025, 15(3), 166; https://doi.org/10.3390/bios15030166 - 4 Mar 2025
Cited by 1 | Viewed by 1065
Abstract
In recent decades, the utilization of biomarkers has gained increasing attention. The timely identification and quantification of proteins, nucleic acids, and small molecules associated with a medical condition, infection, or contaminant have become increasingly crucial across a variety of fields, including medicine, food [...] Read more.
In recent decades, the utilization of biomarkers has gained increasing attention. The timely identification and quantification of proteins, nucleic acids, and small molecules associated with a medical condition, infection, or contaminant have become increasingly crucial across a variety of fields, including medicine, food safety, and quality/environmental control. State-of-the-art biomarker detection methods predominantly rely on standard immunoassay techniques, requiring specialized laboratory equipment and trained personnel. This impedes the broad commercial implementation of biosensors in, e.g., Point-of-Care (PoC) settings where ease of operation, portability, and cost-efficiency are prioritized. Small, robust electrochemical biosensors are a promising alternative for analyzing biomarkers in complex samples within PoC environments. Therefore, creating and designing optimized sensing surfaces, immobilization strategies, and efficient signal generation are crucial for improving biosensor systems, which in turn can have real-world impact. In the present paper, we reviewed common electrode types and geometries used in electrochemical biosensors and the immobilization approaches, discussed the advantages and drawbacks of different electrochemical detection methods, and presented different labeling strategies for signal generation and enhancement. Full article
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