Publication | Closed Access
Reverse Fluorescence Enhancement and Colorimetric Bimodal Signal Readout Immunochromatography Test Strip for Ultrasensitive Large-Scale Screening and Postoperative Monitoring
64
Citations
25
References
2016
Year
Immunocytochemical TechniqueEngineeringPathologyImmunophenotypingNanomedicineQuantitative Fast ScreeningCancer DetectionUltrasensitive Large-scale ScreeningBioanalysisImmunochemistryBiomarker DiscoveryClinical ChemistryPostoperative MonitoringMolecular DiagnosticsLaboratory MedicineRadiologyFluorescence ReadoutTumor TargetingAntibody ScreeningCancer BiomarkersInnovative DiagnosticsMedicineReverse Fluorescence Enhancement
Ultrasensitive and quantitative fast screening of cancer biomarkers by immunochromatography test strip (ICTS) is still challenging in clinic. The gold nanoparticles (NPs) based ICTS with colorimetric readout enables a quick spectrum screening but suffers from nonquantitative performance; although ICTS with fluorescence readout (FICTS) allows quantitative detection, its sensitivity still deserves more efforts and attentions. In this work, by taking advantages of colorimetric ICTS and FICTS, we described a reverse fluorescence enhancement ICTS (rFICTS) with bimodal signal readout for ultrasensitive and quantitative fast screening of carcinoembryonic antigen (CEA). In the presence of target, gold NPs aggregation in T line induced colorimetric readout, allowing on-the-spot spectrum screening in 10 min by naked eye. Meanwhile, the reverse fluorescence enhancement signal enabled more accurately quantitative detection with better sensitivity (5.89 pg/mL for CEA), which is more than 2 orders of magnitude lower than that of the conventional FICTS. The accuracy and stability of the rFICTS were investigated with more than 100 clinical serum samples for large-scale screening. Furthermore, this rFICTS also realized postoperative monitoring by detecting CEA in a patient with colon cancer and comparing with CT imaging diagnosis. These results indicated this rFICTS is particularly suitable for point-of-care (POC) diagnostics in both resource-rich and resource-limited settings.
| Year | Citations | |
|---|---|---|
Page 1
Page 1