辣根过氧化物酶
过氧化物酶
化学
基质(水族馆)
组合化学
量子点
衍生化
核化学
色谱法
纳米技术
酶
材料科学
生物化学
质谱法
海洋学
地质学
作者
Pu Zhang,Wanqiang Xia,Ping Deng,Yuanhong Min,Juan Tan,Yi Wang,Wensheng Fu
标识
DOI:10.1016/j.colsurfb.2021.111953
摘要
Peroxidase-like activity of MoS2 quantum dots (QDs) can be reversibly regulated by means of Fe3+/alendronate sodium (ALDS)-induced aggregation/disaggregation of the QDs in solution. Specifically, Fe3+ can selectively aggregate the MoS2 QDs and thus greatly enhance their peroxidase-like activity, while such enhancement can be inhibited in the presence of ALDS owing to the competitive coordination of ALDS with Fe3+. By regulating the enzyme-like activity of MoS2 QDs, different colorimetric signal of a typical substrate of horseradish peroxidase, 3,3΄,5,5΄-tetramethylbenzidine, can be measured in the presence of H2O2. Based on this mechanism, we develop a colorimetric approach for the determination of ALDS and further applied in quality control of pharmaceutical products, utilizing either smartphone or UV–vis spectrometer as a readout. This detection method is rapid and selective, where derivatization of ALDS before detection is not needed. Such a smartphone-based colorimetric detection platform is promising to be applied in point-of-care testing at home, small clinics, or underdeveloped regions.
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