Chongqing Key Laboratory of High Active Traditional Chinese Drug Delivery System, Chongqing Medical and Pharmaceutical College, Chongqing 401331, China.
School of Chemistry and Chemical Engineering, Chongqing University, Chongqing 401331, China.
Biosensors (Basel). 2022 Oct 18;12(10):893. doi: 10.3390/bios12100893.
In this work, indoxyl-glucoside was used as the substrate to develop a cost-effective, paper-based analytical device for the fluorescent and colorimetric dual-mode detection of β-glucosidase activity through a smartphone. The β-glucosidase can hydrolyze the colorless substrate indoxyl-glucoside to release indoxyl, which will be self-oxidized to generate green products in the presence of oxygen. Meanwhile, the green products emit bright blue-green fluorescence under ultraviolet-visible light irradiation at 365 nm. Fluorescent or colorimetric images were obtained by a smartphone, and the red-green-blue channels were analyzed by the Adobe Photoshop to quantify the β-glucosidase activity. Under the optimum conditions, the relative fluorescent and colorimetric signals have a good linear relationship with the activity of β-glucosidase, in the range of 0.01-1.00 U/mL and 0.25-5.00 U/mL, and the limits of detection are 0.005 U/mL and 0.0668 U/mL, respectively. The activities of β-glucosidase in a crude almond sample measured by the fluorescent and colorimetric methods were 23.62 ± 0.53 U/mL and 23.86 ± 0.25 U/mL, respectively. In addition, the spiked recoveries of normal human serum and crude almond samples were between 87.5% and 118.0%. In short, the paper-based device, combined with a smartphone, can provide a simple, environmentally friendly, and low-cost method for the fluorescent and colorimetric dual-mode detection of β-glucosidase activity.
在这项工作中,我们使用靛基质-葡糖苷作为底物,开发了一种经济高效的基于纸张的分析装置,通过智能手机实现了β-葡萄糖苷酶活性的荧光和比色双模检测。β-葡萄糖苷酶可以水解无色的底物靛基质-葡糖苷,释放出靛基质,在氧气存在的情况下,靛基质会自动氧化生成绿色产物。同时,在 365nm 紫外可见光照射下,绿色产物会发出明亮的蓝绿色荧光。通过智能手机获得荧光或比色图像,并通过 Adobe Photoshop 分析红-绿-蓝通道来定量β-葡萄糖苷酶的活性。在最佳条件下,相对荧光和比色信号与β-葡萄糖苷酶的活性具有良好的线性关系,在 0.01-1.00U/mL 和 0.25-5.00U/mL 的范围内,检测限分别为 0.005U/mL 和 0.0668U/mL。用荧光法和比色法测定的粗杏仁样品中的β-葡萄糖苷酶活性分别为 23.62±0.53U/mL 和 23.86±0.25U/mL。此外,正常人体血清和粗杏仁样品的加标回收率在 87.5%到 118.0%之间。总之,基于纸张的装置与智能手机相结合,可以为β-葡萄糖苷酶活性的荧光和比色双模检测提供一种简单、环保、低成本的方法。