School of Chemistry and Environmental Engineering, Shanxi Datong University, Shanxi, 037009, China.
Key Laboratory of Optic-electric Sensing and Analytical Chemistry for Life Science, MOE; Shandong Key Laboratory of Biochemical Analysis; Key Laboratory of Analytical Chemistry for Life Science in Universities of Shandong; College of Chemistry and Molecular Engineering; College of Marine Science and Biological Engineering, Qingdao University of Science and Technology, Qingdao, 266042, China.
Mikrochim Acta. 2019 Jul 20;186(8):552. doi: 10.1007/s00604-019-3687-z.
Copper(II) polyphthalocyanine (CuPPc) was combined with graphitic carbon nitride (g-CN) to form a heterojunction with enhanced photoelectrochemical (PEC) signal. A sensitive PEC method was developed for determination of ractopamine based on a PEC inner filter effect between gold nanoparticles (AuNPs) and the g-CN/CuPPc. A gold electrode was modified with g-CN/CuPPc and the DNA was linked to the AuNPs. Initially, the PEC signal is weak due to the inner filter effect between the AuNPs and g-CN/CuPPc. In the presence of ractopamine, it interacts with the aptamer and the complementary chain (C chain) is released. This triggers the entropy-driven cyclic amplification and results in the release of the substrate B chain (SB chain) from three-dimensional DNA stabilizer. The probe is released from the electrode due to the interaction of probe DNA and the SB chain. As a result, the PEC signal increases linearly in the 0.1 pmol·L to 1000 pmol·L ractopamine concentration range. The detection limit is 0.03 pM, and the relative standard deviation is 3.4% (at a 10 pmol·Llevel; for n = 11). The method has been successfully applied to the determination of ractopamine in pork samples. Graphical abstract Schematic presentation of detection method based on PEC inner filter effect between AuNPs and the g-CN/CuPPc being fabricated for ractopamine. 3D DNA was used as stabilizer to decrease the PEC blank signal.
铜(II)酞菁(CuPPc)与石墨相氮化碳(g-CN)结合形成具有增强光电化学(PEC)信号的异质结。基于金纳米粒子(AuNPs)与 g-CN/CuPPc 之间的 PEC 内滤效应,建立了一种用于检测莱克多巴胺的灵敏 PEC 方法。金电极修饰有 g-CN/CuPPc,DNA 与 AuNPs 连接。最初,由于 AuNPs 和 g-CN/CuPPc 之间的内滤效应,PEC 信号较弱。在莱克多巴胺存在下,它与适体相互作用,释放互补链(C 链)。这触发了熵驱动的循环扩增,导致三维 DNA 稳定剂从 SB 链释放。由于探针 DNA 和 SB 链的相互作用,探针从电极上释放。因此,在 0.1 pmol·L 至 1000 pmol·L 莱克多巴胺浓度范围内,PEC 信号线性增加。检测限为 0.03 pM,相对标准偏差为 3.4%(在 10 pmol·L 水平;n=11)。该方法已成功应用于猪肉样品中莱克多巴胺的测定。 图表摘要 基于 AuNPs 与 g-CN/CuPPc 之间的 PEC 内滤效应构建用于检测莱克多巴胺的检测方法示意图。3D DNA 用作稳定剂以降低 PEC 空白信号。