AI Article Synopsis

  • Homogeneous electrochemiluminescence (ECL) offers a simple and stable detection method, but false positives from solution interference are a significant problem that researchers are trying to solve.
  • To improve detection, magnetic ECL nanoparticles (FeO@Ru@SiO NPs) were developed, which allow for easy modification and effective separation in a sensor designed for detecting miRNA-155 using tailored DNA molecules to enhance signal clarity.
  • The sensor shows a strong linear correlation between ECL intensity and target concentration (100 fM to 10 nM) and boasts a detection limit of 26.91 fM, suggesting high accuracy for clinical samples and promising future applications in diagnostics.

Article Abstract

Homogeneous electrochemiluminescence (ECL) has gained attention for its simplicity and stability. However, false positives due to solution background interference pose a challenge. To address this, magnetic ECL nanoparticles (FeO@Ru@SiO NPs) were synthesized, offering easy modification, magnetic separation, and stable luminescence. These were utilized in an ECL sensor for miRNA-155 (miR-155) detection, with locked DNAzyme and substrate chain (mDNA) modified on their surface. The poor conductivity of long-chain DNA significantly impacts the conductivity and electron transfer capability of FeO@Ru@SiO NPs, resulting in weaker ECL signals. Upon target presence, unlocked DNAzyme catalyzes mDNA cleavage, leading to shortened DNA chains and reduced density. In contrast, the presence of short-chain DNA has minimal impact on the conductivity and electron transfer capability of FeO@Ru@SiO NPs. Simultaneously, the material surface's electronegativity decreases, weakening the electrostatic repulsion with the negatively charged electrode, resulting in the system detecting stronger ECL signals. This sensor enables homogeneous ECL detection while mitigating solution background interference through magnetic separation. Within a range of 100 fM to 10 nM, the sensor exhibits a linear relationship between ECL intensity and target concentration, with a 26.91 fM detection limit. It demonstrates high accuracy in clinical sample detection, holding significant potential for clinical diagnostics. Future integration with innovative detection strategies may further enhance sensitivity and specificity in biosensing applications.

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Source
http://dx.doi.org/10.1021/acs.analchem.4c02848DOI Listing

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