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基于上转换纳米粒子和磁性纳米粒子的竞争性免疫分析同时检测吡虫啉和噻虫啉

Competitive immunoassay for simultaneous detection of imidacloprid and thiacloprid by upconversion nanoparticles and magnetic nanoparticles.

机构信息

College of Plant Protection, State & Local Joint Engineering Research Center of Green Pesticide Invention and Application, Nanjing Agricultural University, Nanjing, Jiangsu Province, China.

出版信息

Environ Sci Pollut Res Int. 2019 Aug;26(23):23471-23479. doi: 10.1007/s11356-019-05635-8. Epub 2019 Jun 14.

Abstract

A rapid and sensitive immunoassay for the simultaneous detection of imidacloprid and thiacloprid was developed by using magnetic nanoparticles (MNPs) and upconversion nanoparticles (UCNPs). The UCNPs of NaYF:Yb, Er and NaYF:Yb, Tm were synthesized and conjugated with anti-imidacloprid monoclonal antibody (mAb) and anti-thiacloprid mAb as signal labels, while the MNPs were conjugated with antigens of thiacloprid and imidacloprid as separation elements. The fluorescence intensities of Yb/Er- and Yb/Tm-doped UCNPs were detected simultaneously in 544 nm and 477 nm under the excitation of NIR light (980 nm). The amounts of mAb-conjugated UCNPs that were separated by antigen-conjugated MNPs were determined based on competitive immunoassays. Under the optimal conditions, the 50% inhibiting concentration (IC) and limit of detection (LOD, IC) were 5.80 and 0.32 ng/mL for imidacloprid and 6.45 and 0.61 ng/mL for thiacloprid, respectively. The immunoassay exhibited negligible cross-reactivity with analogs of imidacloprid and thiacloprid except imidaclothiz (86.2%). The average recoveries of imidacloprid and thiacloprid in environmental and agricultural samples, including paddy water, soil, pears, oranges, cucumbers, and wheat, ranged from 78.4 to 105.9% with relative standard deviations (RSDs) of 2.1-11.9% for imidacloprid and ranged from 82.5 to 102.3% with RSDs of 1.0-16.5% for thiacloprid. In addition, the results of the immunoassay correlated well with high-performance liquid chromatography for the detection of the authentic samples.

摘要

一种基于磁性纳米粒子(MNPs)和上转换纳米粒子(UCNPs)的同时检测吡虫啉和噻虫啉的快速灵敏免疫分析方法。合成了 NaYF:Yb、Er 和 NaYF:Yb、Tm 的 UCNPs,并将其与抗吡虫啉单克隆抗体(mAb)和抗噻虫啉 mAb 偶联作为信号标记,而 MNPs 则与噻虫啉和吡虫啉的抗原偶联作为分离元件。在近红外光(980nm)激发下,同时检测到 544nm 和 477nm 处 Yb/Er-和 Yb/Tm 掺杂 UCNPs 的荧光强度。基于竞争免疫分析,测定了与抗原偶联的 MNPs 分离的 mAb 偶联 UCNPs 的量。在最佳条件下,吡虫啉的 50%抑制浓度(IC)和检测限(LOD,IC)分别为 5.80 和 0.32ng/mL,噻虫啉的分别为 6.45 和 0.61ng/mL。该免疫分析方法与吡虫啉和噻虫啉的类似物除了噻虫嗪(86.2%)外几乎没有交叉反应性。吡虫啉和噻虫啉在环境和农业样品中的平均回收率,包括稻田水、土壤、梨、橙、黄瓜和小麦,吡虫啉在 78.4%至 105.9%之间,相对标准偏差(RSD)为 2.1%至 11.9%,噻虫啉在 82.5%至 102.3%之间,RSD 为 1.0%至 16.5%。此外,该免疫分析方法与高效液相色谱法检测真实样品的结果相关性良好。

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