研究目的
To develop a dual quantum dots-based ?uorescence-linked immunosorbent assay (dQDs-FLISA) for simultaneous and quantitative detection of in?ammation biomarkers (i.e. serum amyloid A (SAA) and C-reactive protein (CRP)).
研究成果
The dQDs-FLISA method demonstrated high sensitivity, specificity, and accuracy for the simultaneous detection of SAA and CRP biomarkers. It offers great potential for the development of simultaneous and accuracy determination in biomedicines, food safety, and environmental monitoring.
研究不足
The study did not explore the application of the dQDs-FLISA method in clinical settings or its comparison with other established methods for biomarker detection.
1:Experimental Design and Method Selection:
The study utilized quantum dots (QDs) as fluorescence probes for the detection of SAA and CRP biomarkers. The QDs were coated with amphiphilic oligomers (PMAH) to enhance their biocompatibility and stability.
2:Sample Selection and Data Sources:
The study focused on the detection of SAA and CRP biomarkers in serum samples.
3:List of Experimental Equipment and Materials:
Hydrophobic CdSe/ZnS QDs (red-QD) and ZnCdSeS/ZnS QDs (green-QD) were used as fluorescence probes. A SpectraMax i3 Multi-Mode microplate reader was used for reading the photoluminescence (PL) intensity.
4:Experimental Procedures and Operational Workflow:
The dQDs-FLISA method involved coating antibodies on a microplate, adding target antigens, and then adding QD-antibody probes. The PL intensity was measured to determine the concentration of the biomarkers.
5:Data Analysis Methods:
The PL intensity was plotted against the biomarker concentration to establish a standard curve for quantitative analysis.
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