研究目的
To develop a reliable, rapid, and ultrasensitive immunoassay for the determination of immunoglobulin G (IgG) using Fe3O4 superparticle@SiO2 nanocomposites as infrared probes, with improved sensitivity and speed through magnetic field assistance.
研究成果
The Fe3O4 superparticle@SiO2 nanocomposites-based immunoassay provides a sensitive, rapid, and reliable method for IgG detection, with enhanced performance due to magnetic field assistance. It shows high selectivity, specificity, and stability, and is applicable to real blood samples, demonstrating practical utility. Future work should extend the method to other analytes.
研究不足
The applicability of the method to other substances, such as DNAs, bacteria, and pollutants, still needs to be further explored.
1:Experimental Design and Method Selection:
A sandwich immunoassay strategy was designed using Fe3O4 superparticle@SiO2 nanocomposites as IR probes. The method leverages the IR fingerprint signals of SiO2 for detection, with magnetic field assistance to enhance sensitivity and reduce assay time.
2:Sample Selection and Data Sources:
Human IgG was used as the analyte. Blood samples from anonymous volunteers were collected and processed to obtain plasma. Interfering agents like BSA, GLU, LYS, HIgM, and HIgA were used for selectivity tests.
3:List of Experimental Equipment and Materials:
Materials included Fe3O4 nanoparticles, DTAB, PVP, TEOS, APTES, glutaraldehyde, goat-anti-human IgG, human IgG, BSA, and others from suppliers like Sigma Aldrich and Beijing Chemical Works. Equipment included TEM (JEOL JEM-2100), XRD (Rigaku D/MAX 2500), SQUID magnetometer (Quantum Design MPMS-XL), and FTIR spectrometer (Nicolet IS10).
4:0). Experimental Procedures and Operational Workflow:
4. Experimental Procedures and Operational Workflow: Fe3O4 superparticles were prepared via solvophobic method, coated with SiO2 using a one-pot emulsion-droplet-based method, and functionalized with antibodies via glutaraldehyde crosslinking. Gold-coated substrates were prepared and used for antibody immobilization. The immunoassay involved incubating analyte with probes, magnetic separation, capture on substrates with or without magnetic field, and FTIR measurement.
5:Data Analysis Methods:
The integral area of the IR absorption band between 1250 cm?1 and 900 cm?1 was used for quantitative analysis. Detection limits were calculated using the 3Sb/m criterion, and linear correlations were assessed.
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