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March 16, 2026Analytical Chemistry2 citations

Rigid Restriction-Enabled Ultrabright Luminescence through Feather-like Metal-AIEgens Frameworks and Coupling the Collaborative Interfacial Recognition Mechanism for Pathogen Diagnosis

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ZCZhaowen CuiBeijing Jingshida Electromechanical Equipment Research InstituteCNChenyao NieWenzhou Medical UniversityYLYong LiBGI Group (China)

Key Points

  • This research aims to improve the performance and understanding of immunochromatographic assays for pathogen detection.
  • Constructed a featherlike zinc-based metal-AIEgen framework (Zn-TCPE MAF).
  • Measured fluorescent enhancement and quantum yield using spectroscopy.
  • Applied isothermal titration calorimetry to study interfacial recognition mechanisms.
  • Evaluated detection limits and specificity in food samples.
  • Achieved a 4.85-fold increase in fluorescence enhancement with a 9.5-fold increase in quantum yield.
  • Detected a limit of 145 CFU mL⁻¹, over 34 times more sensitive than conventional methods.
  • Demonstrated high specificity, stability, repeatability, and feasibility for practical applications.

Abstract

The pursuit of high-performance immunochromatographic assays (ICAs) is hindered by inadequate signal brightness and the lack of understanding of the nanobiointerfacial recognition mechanism. Herein, a featherlike zinc-based metal-AIEgen framework (Zn-TCPE MAF) to concurrently address these dual challenges is constructed for ultrasensitive Salmonella typhimurium ICA detection. The rigid framework restricts intramolecular motion of the tetraphenylethylene (TCPE) ligand, yielding the fluorescent enhancement by 4.85-fold, ultrabright emitter with a 9.5-fold enhanced quantum yield (44.17%) and prolonging the fluorescent lifetimes from 1.65 to 7.42 ns. The ultrafast electron dynamics mechanism was revealed by femtosecond transient absorption spectroscopy, demonstrating the rigid restriction accelerates the internal conversion process to 247.62 fs, thereby effectively suppressing the nonradiative decay channel. Moreover, isothermal titration calorimetry quantitatively deciphers the interfacial recognition mechanism, revealing a spontaneous (ΔG Ka = 1.72 × 107 M-1) antibody conjugation driven by synergistic electrostatic interaction, hydrogen bonding (ΔH S >0). Leveraging these merits, the fabricated fluorescent ICA strip achieves a detection limit of 145 CFU mL-1, representing a >34-fold sensitivity improvement over conventional AuNP-based strips, with excellent specificity, stability, repeatability, and feasibility in various food samples, paving a synergistic avenue for next-generation ICA diagnostics.

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Cite This Study

Cui et al. (2026) studied this question.

synapsesocial.com/papers/69b79dce8166e15b153aafeehttps://doi.org/10.1021/acs.analchem.5c08233
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