Volume 11 Issue 5
Oct.  2021
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Xingchu Gong, Jingyuan Shao, Shangxin Guo, Jingjing Pan, Xiaohui Fan. Determination of inhibitory activity of Salvia miltiorrhiza extracts on xanthine oxidase with a paper-based analytical device[J]. Journal of Pharmaceutical Analysis, 2021, 11(5): 603-610. doi: 10.1016/j.jpha.2020.09.004
Citation: Xingchu Gong, Jingyuan Shao, Shangxin Guo, Jingjing Pan, Xiaohui Fan. Determination of inhibitory activity of Salvia miltiorrhiza extracts on xanthine oxidase with a paper-based analytical device[J]. Journal of Pharmaceutical Analysis, 2021, 11(5): 603-610. doi: 10.1016/j.jpha.2020.09.004

Determination of inhibitory activity of Salvia miltiorrhiza extracts on xanthine oxidase with a paper-based analytical device

doi: 10.1016/j.jpha.2020.09.004
Funds:

The authors would like to thank the support of the National S&T Major Project of China (Grant No.: 2018ZX09201011), the National Natural Science Foundation of China (Grant No.: 81503242), and the Fundamental Research Funds for the Central Universities (Grant No.: 2018FZA7019).

  • Received Date: Apr. 10, 2020
  • Rev Recd Date: Sep. 20, 2020
  • Available Online: Jan. 11, 2022
  • Publish Date: Oct. 15, 2021
  • A novel paper-based analytical device (PAD) was prepared and applied to determine the xanthine oxidase (XOD) inhibitory activity of Salvia miltiorrhiza extracts (SME). First, polycaprolactone was 3D printed on filter paper and heated to form hydrophobic barriers. Then the modified paper was cut according to the specific design. Necessary reagents including XOD for the colorimetric assay were immobilized on two separate pieces of paper. By simply adding phosphate buffer, the reaction was performed on the double-layer PAD. Quantitative results were obtained by analyzing the color intensity with the specialized device system (consisting of a smartphone, a detection box and sandwich plates). The 3D-printed detection box was small, with a size of 9.0 cm × 7.0 cm × 11.5 cm. Color component G performed well in terms of linearity and detection limits and thus was identified as the index. The reaction conditions were optimized using a definitive screening design. Moreover, a 10% glycerol solution was found to be a suitable stabilizer. When the stabilizer was added, the activity of XOD could be maintained for at least 15 days under 4 °C or −20 °C storage conditions. The inhibitory activity of SME was investigated and compared to that of allopurinol. The results obtained with the PAD showed agreement with those obtained with the microplate method. In conclusion, the proposed PAD method is simple, accurate and has a potential for point-of-care testing. It also holds promise for use in rapid quality testing of medicinal herbs, intermediate products, and preparations of traditional Chinese medicines.
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