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March 16, 2026Exploration0 citationsOpen Access

Spherical Nucleic Acid Stabilized Cage Type Three‐Dimensional Electrochemiluminescence Probe for Sensitive and Amplification‐Free Diagnosis of Infectious Diseases

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YFYu FuWSWenlu SongJLJinyan Lin

Key Points

  • This research aims to develop a rapid and sensitive nucleic acid-based method for diagnosing infectious diseases without amplification.
  • Utilized spherical nucleic acid-stabilized cage-type 3D electrochemiluminescence (ECL) probe
  • Combined the ECL probe with a paper-based bipolar electrode sensor
  • Made surface modifications with polydopamine and SNAs
  • Measured luminous efficiency and detection capabilities against pathogens.
  • Validated effectiveness using Mpox and SARS-CoV-2 clinical samples
  • Achieved 1000-fold enhancement in luminous efficiency compared to ordinary ECL probes.
  • Attained limits of detection as low as 3 copies/µL.
  • Demonstrated 100% sensitivity and specificity against quantitative polymerase chain reaction.
  • Provided results within approximately 15 minutes.

Abstract

ABSTRACT Accurate nucleic acid‐based pathogen diagnosis is critical for clinical treatment and epidemic control. However, present gold‐standard testing methods based on nucleic acid amplification are limited by their time and labor‐intensive nature. Hence, we reported an amplification‐free assay that facilitates rapid, sensitive, and point‐of‐care detection of infectious diseases. Herein, spherical nucleic acid (SNA)‐stabilized cage‐type three‐dimensional electrochemiluminescence (ECL) reporter probe, constructed utilizing Ru(dcbpy) 3 Cl 2 ‐doped NH 2 ‐MIL‐101 (Fe) metal‐organic framework, was combined with a paper‐based bipolar electrode ECL sensor. Furthermore, surface modifications were performed using polydopamine and SNAs to further improve the stability. Notably, compared with the ordinary Ru(dcbpy) 3 Cl 2 , the modified ECL probe attained 10 3 ‐fold enhancement in luminous efficiency. The developed ECL‐based nucleic acid biosensing system offers the advantages of simplicity, portability, low cost, and user‐friendly nucleic acid detection, with a sample‐to‐answer time of approximately 15 min. Additionally, the effectiveness of the developed assay in detecting pathogenic nucleic acid was assessed using Mpox and SARS‐Cov‐2, exhibiting a wide dynamic range from 33 to 10 10 aM and limits of detection as low as 3 copies/µL. Furthermore, the assay exhibited 100% sensitivity and specificity when validated against quantitative polymerase chain reaction‐based detection using clinical samples. Altogether, the findings of this study show the efficacy of the novel developed SNA‐stabilized cage‐type 3D ECL probe‐enhanced nucleic acid assay, along with its potential as a promising paradigm for point‐of‐care diagnosis of infectious pathogens.

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Cite This Study

Fu et al. (2026) studied this question.

synapsesocial.com/papers/69b79e6e8166e15b153abb88https://doi.org/10.1002/exp.20240451
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