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基于注射器辅助适体纳米传感的比色法测定乙酰甲胺磷。

A syringe-aided apta-nanosensing method for colorimetric determination of acetamiprid.

机构信息

State Key Laboratory of Heavy Oil Processing and Center for Bioengineering and Biotechnology, China University of Petroleum (East China), Qingdao, Shandong, 266580, China.

Center for Evidence Identification, Chongqing Public Security Bureau, Chongqing, 401147, China.

出版信息

Anal Chim Acta. 2021 Mar 15;1150:238118. doi: 10.1016/j.aca.2020.11.050. Epub 2020 Dec 1.

Abstract

A syringe-aided apta-nanosensing method is reported for the colorimetric determination of acetamiprid. The method employs double-stranded (ds) DNA-conjugated gold nanoparticle@magnetic agarose beads, i.e., dsDNA-AuNP@MABs as peroxidase-mimicking composite probes, in which the aptamer is indirectly attached to the AuNP surface through its hybridization with complementary DNA (cDNA). Upon contact with the acetamiprid target, the probes can give perceptible color change due to the possible conformation switch from dsDNA's brush-like to cDNA's 'pancake' regime. An "air-spaced pumping" procedure using a syringe equipped with ring magnets as the operation platform was proposed to facilitate the magnetic separation of the sensing probes. Therefore, the analytical steps can be easily accomplished in a syringe, including probe loading, acetamiprid capture and magnetic separation from crude samples, chromogenic reagent loading and colorimetric visualization. Acetamiprid concentration down to 3.3 ppb can be easily identified by the naked eye. The final solution also can be transferred for quantitative measurement. Under spectrometer, the ratio of the absorbance at 652 nm in the presence and absence of acetamiprid (A/A) is linearly related to the acetamiprid concentration in the 0.4-4.5 ppb range. The limit of detection is calculated to be 0.24 ppb. Moreover, satisfactory recoveries ranging from 90.90 to 91.82% with relative standard deviations of ≤2.96% were obtained in analyzing real spiked samples.

摘要

一种基于注射器的适体纳米传感方法被报道用于比色测定乙酰甲胺磷。该方法采用双链(ds)DNA 修饰的金纳米粒子@磁性琼脂糖珠,即 dsDNA-AuNP@MABs,作为过氧化物酶模拟复合探针,其中适体通过与互补 DNA(cDNA)杂交间接连接到 AuNP 表面。当与乙酰甲胺磷靶标接触时,由于 dsDNA 的刷状到 cDNA 的“薄饼”状态的可能构象转换,探针会产生明显的颜色变化。提出了一种使用配备环形磁铁的注射器作为操作平台的“气隙抽吸”程序,以促进传感探针的磁性分离。因此,分析步骤可以很容易地在注射器中完成,包括探针加载、粗样中乙酰甲胺磷的捕获和磁性分离、显色试剂加载和比色可视化。通过肉眼可以轻松识别低至 3.3 ppb 的乙酰甲胺磷浓度。最终溶液也可以转移进行定量测量。在分光光度计下,在有和没有乙酰甲胺磷的情况下 652nm 处的吸光度比(A/A)与 0.4-4.5 ppb 范围内的乙酰甲胺磷浓度呈线性关系。检测限计算为 0.24 ppb。此外,在分析实际加标样品时,回收率在 90.90%至 91.82%之间,相对标准偏差≤2.96%。

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