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The biofunctionalization of sensor surfaces to enable biorecognition capabilities remains a major challenge in developing diagnostic devices. However, efficient surface chemistries applicable to various sensor types remain elusive. In this study, Primary Layer for Universal Sensing (PLUS), a universal coating for bioprobe immobilization designed to enhance sensor functionality across diverse substrates, is introduced. Derived from the mussel-inspired, catechol-based adhesive polydopamine (pDA), PLUS ensures material-independent coating ability. Unlike conventional methods that involve secondary bioprobe immobilization onto a pre-formed pDA layer, PLUS is directly grown from dopamine (DA) and avidin proteins as co-polymerization precursors, resulting in a highly roughened surface with abundant biotin-binding sites. This strategy, combined with end-functionalization using biotinylated antibodies, significantly enhances immunocapture efficiency compared to traditional immunoassays. Furthermore, the PLUS layer interacts effectively with blocking proteins, preventing non-specific binding of unwanted molecules. This ensures reliable biomarker capture even in complex biological samples, such as 50% human serum and plasma. It is envisioned that this bioprobe immobilization technique will play a pivotal role in advancing high-performance sensor adaptability for molecular diagnostics.
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http://dx.doi.org/10.1002/adhm.202501281 | DOI Listing |
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC12417755 | PMC |
Mikrochim Acta
September 2025
Faculty of Science, Shenyang University of Chemical Technology, Shenyang, 110142, China.
A sensitive electrochemical glucose biosensor using ZrO₂@CNTs nanocomposite was developed for real-time metabolism monitoring for athletes. The nanocomposite was prepared by a simple ultrasound-assisted technique, and the glucose oxidase (GOx) was covalently immobilized to improve the biorecognition ability. CNTs treated with acid served as a highly conductive framework, and ZrO₂ nanoparticles can provide structural stability and catalytic performance, thus showing synergistic enhancement of electron transfer kinetics and enzyme loading capacity.
View Article and Find Full Text PDFCell Physiol Biochem
August 2025
Departamento de Procesos Químicos, Alimentos y Biotecnología. Facultad de Ingeniería y Ciencias Aplicadas. Universidad Técnica de Manabí, Portoviejo, Ecuador.
Background/aims: The quantification of amino acids in the dairy industry is necessary for quality control and for the formulation of functional foods. Thus, the development of enzymatic biosensors requires a detailed study of enzyme kinetics. Parameters such as KM and Vmax are necessary to optimize the sensitivity and specificity of the biosensor.
View Article and Find Full Text PDFMikrochim Acta
September 2025
National Research and Development Institute for Chemistry and Petrochemistry ICECHIM, 202 Splaiul Independentei Street, 060021, Bucharest, Romania.
Molecular recognition and determination of vascular cell adhesion molecule-1 (VCAM-1), interleukin-6 (IL-6), and natriuretic peptide C-type (NPPC) are essential for the early prognosis and diagnosis of cardiovascular diseases, especially in young obese populations. Highly sensitive and selective devices characterized by low Limits of quantification are required for their determination in whole blood. Therefore, a 3D stochastic sensor was developed by immobilizing a chitosan hydrogel onto a carbon paste electrode (used as the support matrix for the hydrogel), which was subsequently modified with gold nanoparticles, multi-walled carbon nanotubes, and β-cyclodextrin (β-CD/AuNPs@MWCNT/CS/CPE).
View Article and Find Full Text PDFMikrochim Acta
September 2025
Henan Agricultural University, Zhengzhou, 450002, China.
A dual-mode aptasensor was engineered for aflatoxin B (AFB) detection by functional integration of peroxidase-mimetic Au@CeO core-shell nanostructures with emissive carbon dots (CDs). The Au@CeO nanocomposite, synthesized via spontaneous redox reaction, exhibited enhanced peroxidase-like activity due to abundant Ce/oxygen vacancies facilitating hydroxyl radical generation. The aptasensor utilizes a competitive binding mechanism, where AFB competed with immobilized Au@CeO-CDs-Apt1 probes for binding sites, resulting in inversely proportional colorimetric and fluorescent signals.
View Article and Find Full Text PDFMikrochim Acta
September 2025
College of Medical Technology, Shaanxi University of Chinese Medicine, Xianyang, 712000, Shaanxi, China.
An advanced electrochemical immunosensor platform was designed for the precise quantification of cortisol. The sensor design integrates graphene oxide-silicon carbide (GO-SiC) nanocomposites onto a glassy carbon electrode (GCE). Denatured bovine serum albumin (d-BSA) and an anti-cortisol antibody were immobilized on the GO-SiC/GCE surface as part of the immunosensor's design.
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