纳米酶MIL-100(Fe)酶促双模式检测抗坏血酸

MIL-100(Fe) Nanozyme-Powered Dual Mode Detection of Ascorbic Acid

  • 摘要: 建立了基于纳米酶的分光光度法和智能手机辅助图像比色法检测抗坏血酸. 通过温和反应合成了一种具有纳米酶活性的金属有机骨架材料MIL-100(Fe),并采用红外光谱、扫描电子显微镜和X射线多晶衍射对其进行表征. MIL-100(Fe)作为类过氧化物酶催化H2O2产生羟基自由基进而促使3, 3', 5, 5'-四甲基联苯胺(TMB)氧化变色,而抗坏血酸可消耗羟基自由基从而抑制TMB的氧化,在此过程中溶液颜色变化明显,可见光吸收信号显著. 将MIL-100(Fe)用于分光光度法检测抗坏血酸时,其线性检测范围为2~25 µmol/L,检测限为1.80 µmol/L. 进一步采用智能手机辅助图像比色法检测抗坏血酸时,(G+B)/R值与抗坏血酸浓度在2.5~25 µmol/L范围内呈线性关系,检测限为1.99 µmol/L.

     

    Abstract: A spectrophotometric method based on nanoenzymes and a smartphone-assisted image colourimetric method has been developed to detect ascorbic acid. A metal-organic frameworks MIL-100(Fe) with nano-enzymatic activity was synthesized through a mild reaction and characterized by infrared spectroscopy, scanning electron microscopy and X-ray polycrystalline diffraction. MIL-100(Fe) acts as a peroxidase-like enzyme to catalyze the generation of hydroxyl radicals from H2O2, promoting the oxidative discolouration of 3, 3', 5, 5'-tetramethylbenzidine (TMB), while ascorbic acid can consume the hydroxyl radicals and thus inhibit the oxidation of TMB, which resulted in a noticeable color change in the solution and a significant visible light absorption signal. When MIL-100(Fe) was used for the spectrophotometric detection of ascorbic acid, the linear range was 2~25 µmol/L and the limit of detection was 1.80 µmol/L. The ascorbic acid was further detected by smartphone-assisted image colorimetric, the (G+B)/R value was linearly related to the concentration of ascorbic acid in the range of 2.5~25 µmol/L, and the limit of detection was 1.99 µmol/L.

     

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