Department of Analytical Chemistry, College of Chemistry, Jilin University, Changchun, 130012, China.
Department of Analytical Chemistry, College of Chemistry, Jilin University, Changchun, 130012, China.
Anal Chim Acta. 2018 Dec 18;1039:74-81. doi: 10.1016/j.aca.2018.07.030. Epub 2018 Jul 17.
In this paper, we developed a sensitive sensor for phytic acid (PA) and hydrogen peroxide (HO) detection based on glutathione-functionalized graphene quantum dots (GQDs@GSH). The fluorescence of GQDs@GSH was found to be effectively quenched by Fe ions via photo-induced electron transfer (PET) process. Upon the addition of PA to GQDs@GSH/Fe system, the fluorescence of GQDs@GSH was significantly restored due to the strong chelating and reducing ability of PA, Fe ions could be reduced to Fe ions by PA and formed PA/Fe complex. Therefore, the "off-on" fluorescence method was constructed to detect PA by using GQDs@GSH/Fe as a fluorescent probe. Furthermore, the method can be used for the detection of HO. HO can destroy the chelate structure of PA/Fe, release Fe ions and oxidize Fe ions to produce Fe ions, leading to the fluorescence quenching of GQDs@GSH again. Under optimal conditions, the fluorescence sensing platform showed good linear relationship between the relative fluorescence intensity I/I and the concentration of PA and HO in the range of 0.05-3 μmol L and 0.5-10 μmol L, respectively. The detection limits of PA and HO were 14 nmol L and 0.134 μmol L, respectively. Furthermore, the fluorescence assay method was also applied in real sample analysis and satisfactory results were obtained.
在本文中,我们开发了一种基于谷胱甘肽功能化石墨烯量子点(GQDs@GSH)的灵敏传感器,用于检测植酸(PA)和过氧化氢(HO)。发现 GQDs@GSH 的荧光通过光诱导电子转移(PET)过程被 Fe 离子有效猝灭。当向 GQDs@GSH/Fe 体系中加入 PA 时,由于 PA 具有很强的螯合和还原能力,GQDs@GSH 的荧光得到了显著恢复,Fe 离子可以被 PA 还原为 Fe 离子,并形成 PA/Fe 配合物。因此,构建了一种基于 GQDs@GSH/Fe 作为荧光探针的“关-开”荧光法来检测 PA。此外,该方法可用于检测 HO。HO 可以破坏 PA/Fe 的螯合结构,释放 Fe 离子并将 Fe 离子氧化为 Fe 离子,导致 GQDs@GSH 的荧光再次猝灭。在最佳条件下,荧光传感平台在 0.05-3 μmol/L 和 0.5-10 μmol/L 范围内显示出 PA 和 HO 的相对荧光强度 I/I 与浓度之间的良好线性关系。PA 和 HO 的检测限分别为 14 nmol/L 和 0.134 μmol/L。此外,该荧光分析方法还应用于实际样品分析,获得了令人满意的结果。