Journal
ANALYTICA CHIMICA ACTA
Volume 943, Issue -, Pages 106-113Publisher
ELSEVIER SCIENCE BV
DOI: 10.1016/j.aca.2016.09.015
Keywords
Photoelectrochemical immunosensing; Resonance energy transfer; ZnCdHgSe QDs; Gold nanorods; Prostate specific antigen
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Funding
- National Natural Science Foundation of China [21275166, 21675175]
- Natural Science Foundation of Hubei Province [2015CFA092]
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Gold nanorods (AuNRs) integrated with ZnCdHgSe near-infrared quantum dots (AuNRs-ZnCdHgSe QDs) were successfully synthesized and characterized by transmission electron microscope, X-ray photoelectron spectroscopy, and X-ray diffraction. A glassy carbon electrode was decorated with the aforementioned AuNRs-ZnCdHgSe QDs nanocomposite, which provides a biocompatible interface for the subsequent immobilization of prostate specific antibody (anti-PSA). After being successively treated with glutaraldehyde vapor and bovine serum albumin solution, a photoelectrochemical immunosensing platform based on anti-PSA/AuNRs-ZnCdHgSe QDs/GCE was established. The photocurrent response of ZnCdHgSe QDs was tremendously improved by AuNRs due to the effect of resonance energy transfer which can be deduced from the dependence of the enhanced efficiency on the AuNRs with different length-to-diameter ratios and spectral absorption characteristics. A maximum photocurrent was obtained when the absorption spectrum of AuNRs matched well with the emission spectrum of ZnCdHgSe QDs. A photoelectrochemical immunosensor for prostate specific antigen (PSA) was achieved by monitoring the photocurrent variation. The photocurrent variation before and after being interacted with PSA solution exhibits a good linear relationship with the logarithm of its concentration (logc(PSA)) in the range from 1.0 pg mL(-1) to 50.0 ng mL(-1). The detection limit of this photoelectrochemical immunosensor is able to reach 0.1 pg mL(-1) (S/N = 3). Determining PSA in clinical human serum was also demonstrated by using the developed anti-PSA(BSA)/AuNRs-ZnCdHgSe QDs/GCE electrode. The results were comparable with those obtained from an enzyme-linked immunosorbent assay method. (C) 2016 Elsevier B.V. All rights reserved.
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