A.N. Bach Institute of Biochemistry, Research Centre of Biotechnology of the Russian Academy of Sciences, Leninsky Prospect 33, 119071 Moscow, Russia; Agricultural-Technological Institute, Peoples' Friendship University of Russia, Mikluho-Maklaya Street 8/2, 117198 Moscow, Russia.
A.N. Bach Institute of Biochemistry, Research Centre of Biotechnology of the Russian Academy of Sciences, Leninsky Prospect 33, 119071 Moscow, Russia.
Anal Chim Acta. 2018 May 12;1007:50-60. doi: 10.1016/j.aca.2017.12.023. Epub 2018 Jan 2.
This study presents the joint use of magnetic nanoparticles (MNPs) and gold nanoparticles (GNPs) for double enhancement in a lateral flow immunoassay (LFIA). The study realizes two types of enhancement: (1) increasing the concentration of analytes in the samples using conjugates of MNPs with specific antibodies and (2) increasing the visibility of the label through MNP aggregation caused by GNPs. The proposed strategy was implemented using a LFIA for potato virus X (PVX), a significant potato pathogen. MNPs conjugated with biotinylated antibodies specific to PVX and GNPs conjugated with streptavidin were synthesized and characterized. The LFIAs with and without the proposed enhancements were compared. The double-enhanced LFIA achieved the highest sensitivity, equal to 0.25 ng mL and 32 times more sensitivity than the non-enhanced LFIA (detection limit: 8 ng mL). LFIAs using one of the types of amplification (magnetic concentration without GNPs-causing aggregation or MNP aggregation without the concentration stage) showed intermediate levels of sensitivity. The double-enhanced LFIA was successfully used for PVX detection in potato leaves. The results for PVX detection in the infected plants were similar for the double-enhanced LFIA developed and the conventional LFIA based on the GNP conjugates; however, the new system provided significant coloring enhancement. This study confirmed that a simple combination of MNPs and GNPs has great potential for high-sensitivity detection and could possibly be adopted for LFIAs of other compounds.
本研究提出了将磁性纳米粒子(MNPs)和金纳米粒子(GNPs)联合用于侧向流免疫分析(LFIA)中的双重增强。该研究实现了两种增强方式:(1)使用 MNPs 与特异性抗体的缀合物增加样品中分析物的浓度,(2)通过 GNPs 引起的 MNP 聚集增加标记的可见度。该策略是通过用于马铃薯 X 病毒(PVX)的 LFIA 实现的,PVX 是一种重要的马铃薯病原体。合成并表征了与 PVX 特异性生物素化抗体缀合的 MNPs 和与链霉亲和素缀合的 GNPs。比较了具有和不具有所提出增强的 LFIA。双增强 LFIA 达到了最高的灵敏度,相当于 0.25ng/mL,比未增强 LFIA 的灵敏度高 32 倍(检测限:8ng/mL)。使用一种类型的放大(没有 GNPs 引起聚集的磁性浓度或没有浓度阶段的 MNP 聚集)的 LFIA 显示出中等水平的灵敏度。双增强 LFIA 成功用于马铃薯叶片中的 PVX 检测。开发的双增强 LFIA 和基于 GNPs 缀合物的常规 LFIA 对感染植物中的 PVX 检测结果相似;然而,新系统提供了显著的显色增强。本研究证实,MNPs 和 GNPs 的简单组合具有高灵敏度检测的巨大潜力,并且可能适用于其他化合物的 LFIA。