Ultrasensitive “on-off-on” photoelectrochemical aptasensor for tumor biomarker using BiOI/α-Fe2O3 p-n heterojunction arrays by in-situ regulation of electron donor distance
Precise assay of carcinoembryonic antigen (CEA) is of paramount significance for the diagnosis, treatment, and prognosis of related cancers. Herein, an ultrasensitive “on-off-on” photoelectrochemical (PEC) aptasensor for CEA assay was proposed based on BiOI/α-Fe2O3 p-n heterojunction arrays by in-si...
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Veröffentlicht in: | Sensors and actuators. B, Chemical Chemical, 2023-01, Vol.375, p.132933, Article 132933 |
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Sprache: | eng |
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Zusammenfassung: | Precise assay of carcinoembryonic antigen (CEA) is of paramount significance for the diagnosis, treatment, and prognosis of related cancers. Herein, an ultrasensitive “on-off-on” photoelectrochemical (PEC) aptasensor for CEA assay was proposed based on BiOI/α-Fe2O3 p-n heterojunction arrays by in-situ regulation of electron donor distance. The synthesized BiOI/α-Fe2O3 nanosheet arrays (BiOI/α-Fe2O3 NSAs) were served as photoactive materials, and the special structure facilitates considerably the immobilization of biomolecules. Ferrocene-modified hairpin DNA (Fc-hDNA), as the biorecognition elements and electron donor, was used to bond with CEA aptamer and offer electrons. The distance between Fc and BiOI/α-Fe2O3 NSAs interface can be effectively regulated through the specific recognition of Fc-hDNA and CEA aptamer, which also exhibited an “on-off-on” PEC sensoring model towards the detection of CEA. This method exhibited a wide linear range from 1.0 × 10−4 to 20 ng mL−1, with a low detection limit of 36.89 fg mL−1 for CEA detection. The developed PEC aptasensor has achieved satisfactory results in serum samples, also provide a novel perspective for other disease marker assay.
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•BiOI/α-Fe2O3 NSAs heterojunction were synthesized and served as sensing platform.•On-off-on PEC aptasensor was proposed by in-situ regulating electron donor distance.•The proposed PEC aptasensor possess a rosy analytical performance for CEA assay. |
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ISSN: | 0925-4005 1873-3077 |
DOI: | 10.1016/j.snb.2022.132933 |