Immunosensor detects CD44 in serum with a limit of 93 fg/mL, suggesting effectiveness for early cancer diagnosis.
The rapid and accurate quantification of CD44 in serum is crucial for the early detection and prevention of malignant tumors. In this study, we developed a "signal-on/off" electrochemiluminescence (ECL) immunosensor for the ultrasensitive detection of CD44, leveraging the dual quenching effects of CuFe2O4-NH2-Pd-GOD on Ti3C2Tx@Ni(OH)2-Ru/TPrA nanoarrays. A novel electroactive and catalytic multilayered nanoarray, Ti3C2Tx@Ni(OH)2, was first synthesized and employed as an efficient signal amplifier to accelerate the ECL response by promoting the reaction between Ru(bpy)32+ and tri-n-propylamine radicals (TPrA•). To realize effective signal quenching, the electron transfer from Ti3C2Tx@Ni(OH)2-Ru to CuFe2O4 occurred. This transfer was driven by appropriate energy level matching and light absorption, leading to significant attenuation of the ECL emission. Moreover, glucose oxidase (GOD)-functionalized CuFe2O4 enhanced the in situ generation of H2O2, thereby intensifying the quenching effect. The developed immunosensor exhibited a broad linear range from 0.5 pg/mL to 100 ng/mL with an ultralow detection limit of 93 fg/mL. This proposed strategy offers a novel method for the highly sensitive detection of CD44 and holds promise for broader applications in visual biomarker identification.
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Xie et al. (2025) studied this question.
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