Uricase based fluorometric determination of uric acid based on the use of graphene quantum dot@silver core-shell nanocomposites.
Rong-Mei KongAijun YangQin WangYoujuan WangLin MaFengli QuPublished in: Mikrochimica acta (2017)
The authors describe a fluorescent "turn-on" assay for detection of uric acid (UA) based on the use of graphene quantum dots coated with a shell of silver (GQD@Ag). The fluorescence of the GQDs is quenched by the silver shell. However, if the silver shell was removed via etching with H2O2 (which is produced by uricase catalyzed oxidation of UA), the fluorescence of the GQDs is restored. The resulting increase in fluorescence at 466 nm depends directly on the concentration of H2O2, which, in turn, depends on the concentration of UA. The method allows UA to be quantitated with a 2 μM detection limit. It was applied to the analysis of human urine samples and exhibited satisfactory results. The method is cost-effective, sensitive and selective for UA. In our perception, it provides a useful tool in clinical analysis and may be extended to other assays based on the use of oxidases. Graphical abstract Schematic of the reduction of Ag(I) and the growth of a silver shell on the surface of graphene quantum dots (GQDs) to form a GQD@Ag nanocomposite whose fluorescence is quenched. Uricase catalyzes the oxidation of uric acid (UA) to produce allantoin and H2O2 which etches the silver shell. This results in the release of GQDs and increased fluorescence, allowing quantitative analysis of UA.
Keyphrases
- uric acid
- quantum dots
- energy transfer
- gold nanoparticles
- sensitive detection
- metabolic syndrome
- silver nanoparticles
- single molecule
- visible light
- loop mediated isothermal amplification
- room temperature
- living cells
- carbon nanotubes
- reduced graphene oxide
- high throughput
- fluorescent probe
- hydrogen peroxide
- highly efficient
- high resolution
- real time pcr
- walled carbon nanotubes
- ionic liquid
- mass spectrometry