研究目的
To develop a single-step, non-enzymatic colorimetric assay for the quantification of glucose in blood using in situ growth of Cu2O/Ag nanoparticles, overcoming limitations of existing methods such as the need for enzyme use, expensive materials, and complex procedures.
研究成果
The developed Cu2O/Ag NP-based colorimetric assay enables rapid, sensitive, and specific quantification of glucose in a single step without enzymes. It offers a low-cost alternative with a detection limit of 9.2 μM and linear range of 15-300 μM, validated with blood samples showing no significant difference from commercial methods. This approach has potential for point-of-care glucose monitoring.
研究不足
The assay requires heating at high temperatures (e.g., 95°C), which may not be ideal for all point-of-care settings. There is potential interference from other reducing species in blood, although minimized by BSA. The method's sensitivity and linear range are specific to the optimized conditions and may not cover all clinical glucose levels without dilution.
1:Experimental Design and Method Selection:
The study employs a one-step synthesis method where glucose reduces Cu2+ and Ag+ ions stabilized by 3-MPA and BSA under alkaline conditions to form Cu2O/Ag NPs, with color change monitored via UV-vis absorption at 400 nm. Factors like molar ratios, reaction time, and temperature are optimized.
2:Sample Selection and Data Sources:
Standard glucose solutions (0-200 mM) and blood samples from healthy volunteers are used. Blood samples are collected via finger prick after fasting.
3:List of Experimental Equipment and Materials:
Includes chemicals like AgNO3, Cu(NO3)2, 3-MPA, BSA, NaOH, glucose, and others from suppliers like Sigma-Aldrich and Acros Organics. Equipment includes a μQuant spectrophotometer, H-7100 TEM, JEM-2100F FE-TEM, D8 DISCOVER SSS XRD, PHI 5000 XPS, and a commercial glucose meter.
4:Experimental Procedures and Operational Workflow:
Solutions are prepared by mixing components, adding NaOH, vortexing, heating at specified temperatures (e.g., 95°C for 3 min), and measuring absorbance. For blood analysis, a standard addition method is used with small sample volumes (1 μL).
5:Data Analysis Methods:
UV-vis absorption data are analyzed to construct calibration plots. Statistical analysis includes Student's t-test for comparing results with a commercial glucose meter.
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