School of Chemistry and Chemical Engineering, Guangxi University for Nationalities, Guangxi Key Laboratory of Chemistry and Engineering of Forest Products, Key Laboratory of Guangxi Colleges and Universities for Food Safety and Pharmaceutical Analytical Chemistry, Nanning 530008, China.
School of Chemistry and Chemical Engineering, Guangxi University for Nationalities, Guangxi Key Laboratory of Chemistry and Engineering of Forest Products, Key Laboratory of Guangxi Colleges and Universities for Food Safety and Pharmaceutical Analytical Chemistry, Nanning 530008, China.
Biosens Bioelectron. 2019 Mar 15;129:100-106. doi: 10.1016/j.bios.2018.12.050. Epub 2019 Jan 9.
A dual gears electrochemiluminecence (ECL) aptasensing strategy for multiple selective determination of kanamycin and neocycin was designed on the basis of the combination of kanamycin and neocycin induced dual gears conversion, the loading platform of metal-organic frameworks (MOFs), surface plasmon resonance (SPR) and ECL resonance energy transfer (ERET) between CdS QDs and AuNPs (or PtNPs). In the absence of target, the dual gears were "off". Then the B1-AuNP (gear B) and aptamer 1-PtNPs acted as signal quenching elements to quench ECL intensity due to ERET process. Upon addition of kanamycin, the aptamer 1-PtNPs were removed from the gear gradually, the ECL was enhanced due to SPR process between AuNPs and CdS QDs. After the incubation of aptamer 2, the dual gears were "off" again and ECL intensity was decreased by ERET process between AuNPs and CdS QDs. In the presence of neomycin, dual gears were "on" again, the ECL signal was enhanced by SPR process between AuNPs and CdS QDs. Under optimal condition, the proposed aptasensor exhibited wide linear ranges of kanamycin (10-10 M) and neomycin (10-10 M), and relatively low detection limits to kanamycin (1.7 × 10 M) and neomycin (3.5 × 10 M). The developed aptasensor realized the multiple ECL detection of kanamycin and neomycin with single luminophore, and was successfully applied to the detection of kanamycin and neomycin in food samples.
基于卡那霉素和新霉素诱导的双齿轮转换、金属有机框架(MOFs)的加载平台、表面等离子体共振(SPR)以及 CdS QDs 和 AuNPs(或 PtNPs)之间的电化学发光(ECL)共振能量转移(ERET),设计了一种用于卡那霉素和新霉素的多重选择性测定的双齿轮电化学发光(ECL)适体传感策略。在不存在靶标时,双齿轮处于“关闭”状态。然后,B1-AuNP(齿轮 B)和适体 1-PtNPs 作为信号猝灭元件,由于 ERET 过程,猝灭 ECL 强度。加入卡那霉素后,适体 1-PtNPs 逐渐从齿轮上脱离,由于 AuNPs 和 CdS QDs 之间的 SPR 过程,ECL 增强。孵育适体 2 后,双齿轮再次“关闭”,由于 AuNPs 和 CdS QDs 之间的 ERET 过程,ECL 强度降低。存在新霉素时,双齿轮再次“开启”,由于 AuNPs 和 CdS QDs 之间的 SPR 过程,ECL 信号增强。在最佳条件下,该适体传感器对卡那霉素(10-10 M)和新霉素(10-10 M)表现出较宽的线性范围,对卡那霉素(1.7×10-10 M)和新霉素(3.5×10-10 M)的检测限相对较低。所开发的适体传感器实现了基于单个发光体的卡那霉素和新霉素的多重 ECL 检测,并成功应用于食品样品中卡那霉素和新霉素的检测。