| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 867489 | Biosensors and Bioelectronics | 2012 | 6 Pages |
Prostate specific antigen (PSA) is a valuable tumor marker for prostate cancer screening. In this work, a novel and sensitive resonance light scattering (RLS) spectral assay of PSA was proposed based on PSA aptamer modified gold nanoparticles (AuNPs). The sulfhydryl modified single-strand aptamer could interact with AuNPs, which made the AuNPs stable in high concentration of salt. In pH 7.0 BR buffer solution, the highly selective combination of PSA and AuNPs-labeling aptamer resulted in the aggregation of AuNPs which showed high RLS intensity. Under the optimal conditions, the magnitude of enhanced RLS intensity (ΔIRLS) was proportional to the concentration of PSA in the range from 0.13 to 110 ng/mL, with a detection limit (LOD, 3σ) of 0.032 ng/mL. This developed RLS assay as well as a commercially available enzyme-linked immunosorbent assay (ELISA) kit was successfully applied to the detection of PSA in 15 serum samples, and an excellent correlation of the levels of PSA measured was obtained. This is the first report of the aptamer based RLS assay for PSA and it is also a significant application of instrumental analysis technique.
► Gold nanoparticles (AuNPs) were modified by prostate specific antigen (PSA) aptamer. ► Aptamer interacted with AuNPs, which made AuNPs stable in high concentration of salt. ► The selective combination of PSA and aptamer resulted in the aggregation of AuNPs. ► This developed RLS assay was successfully applied to detect PSA in 15 serum samples. ► The assay possesses the merits of sensitivity, simple, rapidness and cheapness.
