Analytical Chemistry · 2015 · 103 citations · 40 references
EngineeringBiochemistryClinical SciencesBiosensorsNanobiotechnologyNanomaterialsEnzyme-linked Immunosorbent AssayNanomaterial-based BiosensorsOptical BiosensingOptical BiosensorsProstate-specific Antigen TestingRaman SpectroscopyEnzyme-linked Immunosorbent Assay (Elisa)Method Detection LimitNanoparticlesProtein BiomarkersSurface-enhanced Raman ScatteringSurface-enhanced Raman Scattering BiosensingSurface-enhanced Raman SpectroscopyUltrasensitive Detection
Lowering the detection limit is critical to the design of bioassays required for medical diagnostics, environmental monitoring, and food safety regulations. The current sensitivity of standard color-based analyte detection limits the further use of enzyme-linked immunosorbent assays (ELISAs) in research and clinical diagnoses. Here, we demonstrate a novel method that uses the Raman signal as the signal-generating system of an ELISA and combines surface-enhanced Raman scattering (SERS) with silver nanoparticles aggregation for ultrasensitive analyte detection. The enzyme label of the ELISA controls the dissolution of Raman reporter-labeled silver nanoparticles through hydrogen peroxide and generates a strong Raman signal when the analyte is present. Using this assay, prostate-specific antigen (PSA) and the adrenal stimulant ractopamine (Rac) were detected in whole serum and urine at the ultralow concentrations of 10(-9) and 10(-6) ng/mL, respectively. The methodology proposed here could potentially be applied to other molecules detection as well as PSA and Rac.
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