Key Laboratory of Eco-Environments in Three Gorges Reservoir Region (Ministry of Education), School of Chemistry and Chemical Engineering, Southwest University, 2, Tiansheng Road, BeiBei District, Chongqing, 400715, People's Republic of China.
Mikrochim Acta. 2019 Feb 2;186(3):156. doi: 10.1007/s00604-019-3279-y.
A hybrid material composed of guanine-rich single stranded DNA (G-rich ssDNA) and cobalt oxyhydroxide (CoOOH) nanosheets is used as a nanoprobe for fluorometric turn-on detection of ascorbic acid (AA). The CoOOH nanosheets function as a recognition component for AA. The G-rich ssDNA is used to produce a G-quadruplex, and the G-quadruplex/thioflavin T (ThT) complex acts as a fluorescent reporter. In the absence of AA, p-phenylenediamine (PPD) is oxidized to form oxPPD which has a dark red color. It causes the fluorescence of the G-quadruplex/ThT complex to be quenched. However, in the presence of AA, the CoOOH nanosheets of the nanoprobe are preferentially reduced by AA. Hence, PPD is not oxidized, and fluorescence is not quenched. A fluorometric turn-on method was developed based on these findings. It has a detection limit of 94 nM and works in the concentration range from 1 to 10 and 20 to 80 μM. This method was applied to the determination of AA in (spiked) fruit juice samples. Graphical abstract Schematic presentation of a fluorescent assay of ascorbic acid (AA) is established using a nanoprobe composed of guanine-rich single stranded DNA (G-rich ssDNA) and cobalt oxyhydroxide (CoOOH) nanosheets. It is based on competitive reduction of CoOOH by p-phenylenediamine (PPD) and AA. Thioflavine T (ThT) induces the formation of fluorescent G-quadruplex/ThT complex. The oxidized form of PPD (oxPPD) can quench the fluorescence via fluorescence resonance energy transfer (FRET), but AA suppresses quenching.
一种由富含鸟嘌呤的单链 DNA(G-富 ssDNA)和钴氢氧化物(CoOOH)纳米片组成的杂化材料被用作荧光开启检测抗坏血酸(AA)的纳米探针。CoOOH 纳米片作为 AA 的识别组件。G-富 ssDNA 用于产生 G-四链体,G-四链体/硫黄素 T(ThT)复合物作为荧光报告子。在没有 AA 的情况下,对苯二胺(PPD)被氧化形成深红色的 oxPPD,其导致 G-四链体/ThT 复合物的荧光猝灭。然而,在存在 AA 的情况下,纳米探针的 CoOOH 纳米片优先被 AA 还原。因此,PPD 不会被氧化,荧光不会被猝灭。基于这些发现,开发了一种荧光开启方法。它的检测限为 94 nM,在 1 到 10 和 20 到 80 μM 的浓度范围内有效。该方法用于测定(加标)果汁样品中的 AA。示意图 使用由富含鸟嘌呤的单链 DNA(G-富 ssDNA)和钴氢氧化物(CoOOH)纳米片组成的纳米探针建立了抗坏血酸(AA)的荧光测定法。它基于 CoOOH 被对苯二胺(PPD)和 AA 竞争还原。硫黄素 T(ThT)诱导荧光 G-四链体/ThT 复合物的形成。PPD 的氧化形式(oxPPD)可以通过荧光共振能量转移(FRET)猝灭荧光,但 AA 抑制猝灭。