State Key Laboratory of Biobased Material and Green Papermaking, Qilu University of Technology, Shandong Academy of Sciences, Jinan, 250353, China.
School of Food Science and Engineering, Qilu University of Technology, Shandong Academy of Sciences, Jinan, 250353, China.
Mikrochim Acta. 2019 Jul 20;186(8):555. doi: 10.1007/s00604-019-3643-y.
A dual-mode aptasensor was employed for ultrasensitive determination of sulfamethazine (SMZ). The assay is based on simultaneous quantification by using fluorometry and chirality. The aptamer against SMZ was immobilized on upconversion nanoparticles (UCNPs) while the complementary DNA of SMZ aptamer was immobilized on Au@Ag@Au core-shell nanoparticles (Au@Ag@AuNPs). Based on complementary base-pairing reactions, the aptamer of SMZ and its complementary DNA sequence (cDNA) were hybridized to form duplex structure. Thus, Au@Ag@AuNPs and UCNPs were in close proximity. Efficient inner filter effect (IFE) from UCNPs (energy donor) to Au@Ag@AuNPs (energy acceptor) occurred under the excitation of 980 nm laser. In the presence of targets (SMZ), as the aptamer of SMZ coupled with SMZ to form stable complex structure. As a result, the hybridization of aptamer and its cDNA deceased and the fluorescence signal recovered. Furthermore, as the degree of the assembly decreased, the circular dichroism (CD) signal also decreased. Fluorescence was measured at excitation/emission wavelengths of 980/655 nm. The linear ranges for detection of SMZ are between 0.10-100 ng·mL and 1.00-100 ng·mL for the fluorescence and circular dichroism modes, respectively. The method was applied to the determination of SMZ in spiked milk with high recoveries. Conceivably, it can be extended to the analysis of numerous other targets for which adequate antibodies or aptamers are available. Graphical abstract Schematic representation of a chirality assay and a fluorometric assay based on inner filter effect (IFE) between upconversion nanoparticles (UCNPs) and Au@Ag@Au core-shell nanoparticles (Au@Ag@AuNPs) for the determination of sulfamethazine (SMZ).
一种双模适体传感器被用于磺胺甲恶唑(SMZ)的超灵敏测定。该测定法基于荧光法和手性同时定量。磺胺甲恶唑适体固定在上转换纳米粒子(UCNPs)上,而磺胺甲恶唑适体的互补 DNA 固定在 Au@Ag@Au 核壳纳米粒子(Au@Ag@AuNPs)上。基于互补碱基配对反应,SMZ 的适体与其互补 DNA 序列(cDNA)杂交形成双链结构。因此,Au@Ag@AuNPs 和 UCNPs 非常接近。在 980nm 激光激发下,UCNPs(能量供体)到 Au@Ag@AuNPs(能量受体)发生有效的内滤效应(IFE)。在存在靶标(SMZ)的情况下,由于 SMZ 的适体与 SMZ 结合形成稳定的复合物结构。结果,适体与其 cDNA 的杂交减少,荧光信号恢复。此外,由于组装程度降低,圆二色性(CD)信号也降低。荧光在 980/655nm 的激发/发射波长下进行测量。荧光和圆二色两种模式下,SMZ 的检测线性范围分别为 0.10-100ng·mL 和 1.00-100ng·mL。该方法用于测定加标牛奶中的 SMZ,回收率高。可以想象,它可以扩展到分析大量其他有足够抗体或适体的目标。 图表摘要 基于上转换纳米粒子(UCNPs)和 Au@Ag@Au 核壳纳米粒子(Au@Ag@AuNPs)之间的内滤效应(IFE),用于磺胺甲恶唑(SMZ)测定的手性分析和荧光分析示意图。