TY - JOUR
T1 - Current status and future challenges of transition-metal oxides as enzyme-mimetics for detection of clinically relevant biomarkers
T2 - a comprehensive review
AU - Arivazhagan, Mani
AU - Paramasivam, Shanmugam
AU - Gnanasekaran, Lalitha
AU - D, Shanmugapriya
AU - Prabu, Samikannu
AU - Boonyuen, Supakorn
AU - Ravikumar, Ayyanu
AU - Amalraj, Arunjegan
AU - Jakmunee, Jaroon
N1 - Publisher Copyright:
© The Author(s), under exclusive licence to Springer-Verlag GmbH Austria, part of Springer Nature 2026.
PY - 2026/2
Y1 - 2026/2
N2 - Emerging technologies in healthcare are driving the rapid evolution of advanced sensing and diagnostic systems, paving the way for faster and more accurate predictive and preventive medical applications. The recent identification of numerous biomarkers is linked with early disease detection and screening via real samples. These biomarkers are early warning systems, providing reliable and precise insights into the presence and progression of diseases. In recent years, the strategic utilization of functional transition metal oxides-based nanomaterials are diverse and in combination with electroanalytical techniques have enabled the rapid, sensitive, and selective detection and monitoring of a broad spectrum of biomarkers in body fluids. Given the trace-level concentrations of many biomarkers in bodily fluids, the implementation of signal amplification techniques is critical to enhance detection sensitivity and ensure accurate biomarker quantification. Transition metal oxides-based nanostructures are widely employed to enhance signal output in electrochemical biomarker detection, owing to their excellent catalytic properties and high surface-to-volume ratios. To improve signal sensitivity in electrochemical biomarker detection, transition metal oxide nanostructures are frequently utilized due to their superior electrocatalytic activity, high conductivity, and large active surface areas. This review will examine the recent developments and trends in the use of transition metal oxides for electrochemical biomarker detection via enzyme-mimetics strategy.
AB - Emerging technologies in healthcare are driving the rapid evolution of advanced sensing and diagnostic systems, paving the way for faster and more accurate predictive and preventive medical applications. The recent identification of numerous biomarkers is linked with early disease detection and screening via real samples. These biomarkers are early warning systems, providing reliable and precise insights into the presence and progression of diseases. In recent years, the strategic utilization of functional transition metal oxides-based nanomaterials are diverse and in combination with electroanalytical techniques have enabled the rapid, sensitive, and selective detection and monitoring of a broad spectrum of biomarkers in body fluids. Given the trace-level concentrations of many biomarkers in bodily fluids, the implementation of signal amplification techniques is critical to enhance detection sensitivity and ensure accurate biomarker quantification. Transition metal oxides-based nanostructures are widely employed to enhance signal output in electrochemical biomarker detection, owing to their excellent catalytic properties and high surface-to-volume ratios. To improve signal sensitivity in electrochemical biomarker detection, transition metal oxide nanostructures are frequently utilized due to their superior electrocatalytic activity, high conductivity, and large active surface areas. This review will examine the recent developments and trends in the use of transition metal oxides for electrochemical biomarker detection via enzyme-mimetics strategy.
KW - Biomarkers
KW - Body fluids
KW - Clinical diagnostics
KW - Electroanalytical techniques
KW - Excellent catalytic activity
KW - Physiological conditions
KW - Transition metallic oxides
UR - https://www.scopus.com/pages/publications/105029054759
U2 - 10.1007/s00604-026-07876-0
DO - 10.1007/s00604-026-07876-0
M3 - Review article
C2 - 41619088
AN - SCOPUS:105029054759
SN - 0026-3672
VL - 193
JO - Microchimica Acta
JF - Microchimica Acta
IS - 2
M1 - 118
ER -