Colorimetric and visual determination of uric acid based on decolorization of manganese dioxide nanosheet dispersions.
Rongjing HuTianmin GuoChenyi ZengXiaolong FuBinhua DongZhenyu LinYongqiang DongFengfu FuPublished in: Mikrochimica acta (2023)
Serum levels of uric acid (UA) play an important role in the prevention of diseases. Developing a rapid and accurate way to detect UA is still a meaningful task. Hence, positively charged manganese dioxide nanosheets (MnO 2 NSs) with an average latter size of 100 nm and an ultra-thin thickness of below 1 nm have been prepared. They can be well dispersed in water and form stable yellow-brown solutions. The MnO 2 NSs can be decomposed by UA via redox reaction, leading to a decline of a characteristic absorption peak (374 nm) and a color fading of MnO 2 NSs solution. On this basis, an enzyme-free colorimetric sensing system for the detection of UA has been developed. The sensing system shows many advantages, including a wide linear range of 0.10-50.0 μmol/L, a limit of quantitation (LOQ) of 0.10 μmol/L, a low limit of detection (LOD) of 0.047 μmol/L (3σ/m), and rapid response without need of strict time control. Moreover, a simple and convenient visual sensor for UA detection has also been developed by adding an appropriate amount of phthalocyanine to provide a blue background color, which helps to increase visual discrimination. Finally, the strategy has been successfully applied to detect UA in human serum and urine samples.
Keyphrases
- uric acid
- loop mediated isothermal amplification
- sensitive detection
- photodynamic therapy
- metabolic syndrome
- label free
- gold nanoparticles
- quantum dots
- real time pcr
- hydrogen peroxide
- high resolution
- solid phase extraction
- liquid chromatography tandem mass spectrometry
- mass spectrometry
- nitric oxide
- light emitting
- living cells
- highly efficient
- metal organic framework
- single molecule
- tandem mass spectrometry
- liquid chromatography
- molecularly imprinted
- oxide nanoparticles