Publication | Closed Access
Sensitive Detection of a Tumor Marker, α-Fetoprotein, with a Sandwich Assay on a Plasmonic Chip
65
Citations
20
References
2015
Year
EngineeringMetal NanoparticlesPathologyPeptide ScienceBiosensing SystemsCancer DetectionBioanalysisAnalytical ChemistryBioimagingBiomarker DiscoveryClinical ChemistryNanosensorMolecular DiagnosticsBiophysicsNanophotonicsPlasmonic MaterialPlasmonic ChipBiomedical AnalysisGold Plasmonic ChipAntibody ScreeningOptical SensorsBiomolecular EngineeringSandwich AssayPlasmonicsBiomedical DiagnosticsBiomarkersTumor MarkerMedicineSilver Plasmonic Chip
Two types of plasmonic silver- and gold-coated grating biosensor chips (plasmonic chip) were applied in the detection of α-fetoprotein (AFP) with a sandwich imunoassay and surface plasmon field-enhanced fluorescence. On the plasmonic chip, unlabeled marker in the sandwich immunoassay was first quantitatively detected over a wide range between 10(-12) and 10(-8) g/mL. The affinity constants between AFP and anti-AFP antibody, which were obtained by fitting the experimental data to the Langmuir isotherm adsorption curve, were 1 × 10(8) g(-1) mL regardless of the kind of metal in the plasmonic chips. Although the fluorescence intensity on the silver plasmonic chip was 5 times larger than that on the gold plasmonic chip, the limit of detection (LOD) was on the order of 10(-11) g/mL and not improved with a silver plasmonic chip. Herein, we used a new setup that generated less dispersions of both the fluorescence intensity for nonspecific adsorption and the background (optical blank) signal and improved the LOD of AFP to 4 pg/mL (55 fM) with the silver plasmonic chip. With the highly sensitive detection in the sandwich immunoassay, the development of a plasmonic chip for clinical diagnosis by a blood test is promising.
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