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Rapid Nanoprobe Signal Enhancement by In Situ Gold Nanoparticle Synthesis
Published on: March 7, 2018
Multifunctional Nanozyme with Aptamer-Based Ratiometric Fluorescent and Colorimetric Dual Detection of
Peng Liu1, Linqing Du2,3, Fang Luan2,3
1Key Laboratory for Special Functional Aggregate Materials of Education Ministry, School of Chemistry and Chemical Engineering, Shandong University, Jinan, Shandong 250100, China.
Abstract:
The adsorption of DNA probes onto nanomaterials represents a promising bioassay technique, generally employing fluorescence or catalytic activity to generate signals. A significant challenge is maintaining the catalytic activity of chromogenic catalysts during detection while enhancing accuracy by overcoming the limitations of single-signal transmission. This article presents an innovative multimodal analysis approach that synergistically combines the oxidase-like activity of Fe-N-C nanozyme (Fe-NC) with red fluorescent carbon quantum dots (R-CQDs), further advancing the dual-mode analysis method utilizing R-CQDs@Fe-NC. In this system, R-CQDs integrate with Fe-NC to provide a steady reference red fluorescence signal, while Fe-NC serves as the catalytic active site. The adsorption of 6-carboxyfluorescein-labeled aptamers (FAM-apt) significantly enhanced the electron transfer capability of R-CQDs@Fe-NC, enhancing its catalytic performance and resulting in increased oxidation of 3,3',5,5'-tetramethylbenzidine (TMB). Concurrently, the green fluorescence of FAM-apt diminishes due to energy competition, photoinduced electron transfer, and the internal filtration effect by R-CQDs@Fe-NC, while the red fluorescence from R-CQDs@Fe-NC remains stable. Upon recognizing and binding to prostate-specific antigen (PSA), FAM-apt detaches from the surface of R-CQDs@Fe-NC. This leads to simultaneous variations in both the fluorescence signal of the system and the colorimetric signal of TMB. Based on these properties, a colorimetric/fluorescence dual-mode detection method for PSA was established, with detection limits of 0.054 and 0.16 ng/mL, respectively. Furthermore, a smartphone-based sensing device facilitated rapid and convenient detection. This study presents a multisignal output sensing strategy and a simple capillary sensing device, presenting a promising approach for PSA diagnostic analysis and the potential detection of other biomarkers.

