2D-porphrinic covalent organic framework-based aptasensor with enhanced photoelectrochemical response for the detection of C-reactive protein
In this study, a novel photoelectrochemical (PEC) aptasensor based on two-dimensional (2D) porphyrinic covalent organic frameworks (p-COFs) for the label-free detection of C-reactive protein (CRP) is presented. The obtained p-COFs possess high conductivity and an improved stability due to strong and...
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Veröffentlicht in: | Biosensors & bioelectronics 2019-03, Vol.129, p.64-71 |
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Sprache: | eng |
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Zusammenfassung: | In this study, a novel photoelectrochemical (PEC) aptasensor based on two-dimensional (2D) porphyrinic covalent organic frameworks (p-COFs) for the label-free detection of C-reactive protein (CRP) is presented. The obtained p-COFs possess high conductivity and an improved stability due to strong and rigid covalent linkages. The introduction of p-COFs hinder the recombination of electrons and holes, decreasing their band gap (Eg), thereby which improved the photocurrent conversion efficiency. Compared with pure porphyrin, p-COFs exhibited enhanced photocurrent intensity. An amplified photocurrent conversion efficiency and enhanced photocurrent results from H2O2, which act as active molecules and electron donors. As an unprecedented application of COFs in PEC bioanalysis, the detection of CRP with a PEC aptasensor is presented. The assembly of a CRP aptamer on the surface of Ag nanoparticles hinders the electron transfer, resulting in the decrease of the photocurrent response. This PEC aptasensor exhibits good analytical performances such as a rapid response, high stability, wide linear range and excellent selectivity, making COFs promising candidates for PEC bioanalysis.
•A novel PEC aptasensor based on 2Dp-COFsfor the label-free detection of CRP is presented.•Compared with pure porphyrin, p-COFs exhibited enhanced photocurrent intensity.•The obtained p-COFs possess high conductivity and an improved stability due to strong and rigid covalent linkages.•The improved photocurrent conversion efficiency and photocurrent intensity could be amplified by active molecules. |
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ISSN: | 0956-5663 1873-4235 |
DOI: | 10.1016/j.bios.2019.01.009 |