Chongqing Engineering Laboratory of Nanomaterials & Sensor Technologies, College of Chemistry and Chemical Engineering, Southwest University, Chongqing, 400715, People's Republic of China.
Faculty of Geosciences and Environmental Engineering, Southwest Jiaotong University, Chengdu, 611756, China.
Mikrochim Acta. 2020 Mar 18;187(4):237. doi: 10.1007/s00604-020-4212-0.
The poly[(9,9-dioctylfuorenyl-2,7-diyl)-alt-co-(1,4-benzo-{2,1',3}-thiadiazole)] (PFBT) was carboxyl-functionalized to prepare polymer dots (C-PFBT Pdots), which served as a self-ECL emitter for producing an extraordinary ECL signal without any exogenous coreactants. The C-PFBT Pdots-modified electrode captured the substrate DNA and further hybridized with a ferrocene (Fc)-labeled DNA. The ECL emission of C-PFBT Pdots was quenched by Fc (a signal off state). After the DNAzyme was added, the DNAzyme-substrate hybrids were formed through hybridizing between DNAzyme and substrate and the Fc-labeled DNA was released. In the presence of target Pb, the DNAzyme-substrate hybrids could be specifically recognized and cleaved to release the DNAzyme and Pb. Ultimately, the released DNAzyme would further hybridize with the substrate for producing the DNAzyme-substrate hybrids and then were cleaved by the released Pb. As a result, the DNA walking machine was generated and the substantial Fc was away from C-PFBT Pdots to obtain a signal on state. Such a strategy achieved a sensitive detection of Pb and the detection limit was as low as 0.17 pM. Moreover, making this ECL biosensor for an intracellular Pb detecting, a convincing performance was achieved. The self-ECL emitter C-PFBT Pdots combining with the quencher Fc provided a new strategy and platform for constructing a coreactant-free ECL assay.
聚[(9,9-二辛基芴-2,7-二基)-交替-共-(1,4-苯并-[2,1',3]-噻二唑)](PFBT)被羧基官能化以制备聚合物点(C-PFBT Pdots),它用作自 ECL 发射器,无需任何外源共反应剂即可产生非凡的 ECL 信号。C-PFBT Pdots 修饰电极捕获底物 DNA,然后与二茂铁(Fc)标记的 DNA 进一步杂交。C-PFBT Pdots 的 ECL 发射被 Fc(信号关闭状态)猝灭。加入 DNA 酶后,通过 DNA 酶与底物杂交形成 DNA 酶-底物杂交体,释放 Fc 标记的 DNA。在存在靶 Pb 的情况下,DNA 酶-底物杂交体可以被特异性识别和切割以释放 DNA 酶和 Pb。最终,释放的 DNA 酶将进一步与底物杂交以产生 DNA 酶-底物杂交体,然后被释放的 Pb 切割。结果,生成了 DNA 行走机器,大量 Fc 远离 C-PFBT Pdots 以获得信号开启状态。该策略实现了对 Pb 的灵敏检测,检测限低至 0.17 pM。此外,该 ECL 生物传感器用于细胞内 Pb 检测,取得了令人信服的效果。自 ECL 发射器 C-PFBT Pdots 与猝灭剂 Fc 相结合,为构建无共反应剂的 ECL 分析提供了一种新策略和平台。