3D label-free prostate specific antigen (PSA) immunosensor based on graphene–gold composites
Highly sensitive and label-free detection of the prostate specific antigen (PSA) remains a challenge in the diagnosis of prostate cancer. Here, a novel three-dimensional (3D) electrochemical immunosensor capable of sensitive and label-free detection of PSA is reported. This unique immunosensor is eq...
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Veröffentlicht in: | Biosensors & bioelectronics 2015-01, Vol.63, p.546-551 |
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Sprache: | eng |
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Zusammenfassung: | Highly sensitive and label-free detection of the prostate specific antigen (PSA) remains a challenge in the diagnosis of prostate cancer. Here, a novel three-dimensional (3D) electrochemical immunosensor capable of sensitive and label-free detection of PSA is reported. This unique immunosensor is equipped with a highly conductive graphene (GR)-based gold (Au) composite modified electrode. The GR-based Au composite is prepared using aerosol spray pyrolysis and the morphology of the composite is the shape of a crumpled GR ball decorated with Au nanoparticles. Unlike the previous research, this novel 3D immunosensor functions very well over a broad linear range of 0–10ng/mL with a low detection limit of 0.59ng/mL; furthermore, it exhibits a significantly increased electron transfer and high sensitivity toward PSA. The highest rate of current change with respect to the PSA concentration is 5μA/(ng/mL). Satisfactory selectivity, reproducibility, and stability of the 3D immunosensor are also exhibited.
•A novel 3D label-free PSA immunosensor based on GR–Au composites was successfully developed for the detection of prostate cancer.•The GR-based Au composite is prepared using aerosol spray pyrolysis and the morphology of the composite is the shape of a crumpled GR ball decorated with Au nanoparticles.•The amperometric response of the 3D label-free PSA immunosensor exhibited stronger redox, higher current flow, and smaller electron transfer resistance compared with the 2D GR–Au modified electrode. |
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ISSN: | 0956-5663 1873-4235 |
DOI: | 10.1016/j.bios.2014.08.008 |