State Key Laboratory of Food Science and Technology, Jiangnan University, Wuxi, 214122, China.
School of Food Science and Technology, Jiangnan University, Wuxi, 214122, China.
Mikrochim Acta. 2020 Mar 12;187(4):222. doi: 10.1007/s00604-020-4204-0.
This paper describes the fabrication of an imprinted fluorescent nanoprobe based on SiO-coated NaYF: Yb, Er upconversion nanoparticles (UCNP) encapsulated with a molecularly imprinted polymer (MIP) for determination of acetamiprid. The fluorescent MIP nanoprobe was prepared using UCNP as the material for fluorescence signal readout, acetamiprid as template molecule, methylacrylic acid (MAA) as functional monomer, and ethyleneglycol dimethacrylate (EGDMA) as cross-linking agent. The molecular imprinting layers were immobilized on the surface of the UCNP@SiO by polymerization which occurred between the double bonds. UCNP@MIP shows a high selectivity towards acetamiprid with an imprinting factor (IF) of 7.84. When UCNP@MIP combines with acetamiprid, the fluorescence of the UCNP@MIP can be quenched due to the photo-induced electron transfer. Under optimum conditions, the fluorescence method shows a good linear relationship between the decreased fluorescence intensity (with excitation/emission peaks at 980/542 nm) and the variation of acetamiprid in the concentration range 20 to 800 ng mL. The limit of detection (LOD) is 8.3 ng mL. This fluorescence method was also successfully applied to detect acetamiprid in apple and strawberry samples. The recoveries range from 89.6 to 97.9%, with relative standard deviations between 1.6 and 2.9% (n = 5). Graphical abstractA simple fluorescence nanoprobe which integrates upconversion nanoparticles (UCNPs) and molecular imprinting polymer (MIP) was developed for the determination of acetamiprid. The limit of the detection was determined as 8.3 ng mL. The selectivity was enhanced by molecular imprinting, and the sensitivity was improved by the high sensitivity of the fluorescence emitted from the UCNPs.
本文描述了一种基于 SiO 包覆的 NaYF:Yb,Er 上转换纳米粒子(UCNP)的印迹荧光纳米探针的制备,该探针用于测定啶虫脒。荧光 MIP 纳米探针的制备以 UCNP 为荧光信号读出材料,以啶虫脒为模板分子,甲基丙烯酸(MAA)为功能单体,乙二醇二甲基丙烯酸酯(EGDMA)为交联剂。印迹层通过双键之间的聚合反应固定在 UCNP@SiO 的表面上。UCNP@MIP 对啶虫脒具有高选择性,印迹因子(IF)为 7.84。当 UCNP@MIP 与啶虫脒结合时,由于光诱导电子转移,UCNP@MIP 的荧光会被猝灭。在最佳条件下,荧光法在 20 至 800ng mL 范围内,随着啶虫脒浓度的变化,荧光强度(激发/发射峰在 980/542nm 处)的降低与荧光强度之间呈现良好的线性关系。检测限(LOD)为 8.3ng mL。该荧光法还成功应用于苹果和草莓样品中啶虫脒的检测。回收率在 89.6%至 97.9%之间,相对标准偏差在 1.6%至 2.9%之间(n=5)。