研究目的
Developing a simple, easy-to-operate, and real-time detection method for flavonoids in herbal medicines based on the specific interaction between flavonoids and bovine serum albumin (BSA) using fluorescent gold nanoclusters (AuNCs).
研究成果
The BSA-AuNCs sensing platform offers a rapid, sensitive, and selective method for flavonoid detection, with potential applications in pharmaceutical analysis and biological sample testing.
研究不足
The method may be affected by interferents in complex matrices like urine, as indicated by variable recovery rates for some flavonoids.
1:Experimental Design and Method Selection
The study utilized the specific interaction between flavonoids and BSA to develop a fluorescent detection method. BSA-AuNCs were synthesized as fluorescent probes, and their fluorescence quenching by flavonoids was measured.
2:Sample Selection and Data Sources
Flavonoids including quercetin, apigenin, nobiletin, baicalein, rutin, and wogonin were used. Biological samples (serum, plasma) and a proprietary Chinese medicine (Rutin Tablets) were tested.
3:List of Experimental Equipment and Materials
Chloroauric acid (HAuCl4.3H2O), BSA, various flavonoids, alkaloids, and saponins. Equipment included a fluorimeter (SpectraMax M5e), TEM (JEL-1400), and dynamic light scattering instrument (Litesizer 500).
4:Experimental Procedures and Operational Workflow
AuNCs were synthesized and mixed with flavonoids. Fluorescence intensity was measured immediately after mixing. The method was applied to detect flavonoids in biological samples and Rutin Tablets.
5:Data Analysis Methods
Fluorescence intensity changes were analyzed to determine flavonoid concentrations. Standard curves were established for quantification.
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