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基于发光镧系纳米粒子的成像技术可实现超灵敏、定量和多重侧向流动免疫分析。

Luminescent lanthanide nanoparticle-based imaging enables ultra-sensitive, quantitative and multiplexed lateral flow immunoassays.

作者信息

Mousseau F, Féraudet Tarisse C, Simon S, Gacoin T, Alexandrou A, Bouzigues C I

机构信息

Laboratoire d'Optique et Biosciences, Ecole Polytechnique, Institut Polytechnique de Paris, CNRS, INSERM, Route de Saclay, 91128 Palaiseau, France.

Université Paris-Saclay, CEA, INRAE, Département Médicaments et Technologies pour la Santé (DMTS), 91191 Gif-sur-Yvette, France.

出版信息

Nanoscale. 2021 Sep 17;13(35):14814-14824. doi: 10.1039/d1nr03358a.

Abstract

Lateral Flow Assays (LFAs) have been extensively used on-site to rapidly detect analytes, possibly in complex media. However, standard gold nanoparticle-based LFAs lack sensitivity and cannot provide quantitative measurements with high accuracy. To overcome these limitations, we image lanthanide-doped nanoparticles (YVO:Eu 40%) as new luminescent LFA probes, using a homemade reader coupled to a smartphone and propose an original image analysis allowing strip quantification regardless of the shape of the test band signal. This method is demonstrated for the detection of staphylococcal enterotoxins SEA, SEG, SEH, and SEI. A systematic comparison to state-of-the-art gold nanoparticle-based LFA revealed an analytical sensitivity enhancement of at least one order of magnitude. We furthermore provided measurements of absolute toxin concentration over two orders of magnitude and demonstrated simultaneous quantitative detection of multiple toxins with unaltered sensitivity. In particular, we reached concentrations 100 times lower than the ones reported in the literature for on-site multiplexed LFA targeting enterotoxins. Altogether, these results highlight that our luminescent nanoparticle-based method provides a powerful and versatile on-site framework to detect multiple biomolecules with sensitivity approaching that obtained by ELISA. This paves the way to a change of paradigm in the field of analytical immunoassays by providing fast quantitative high sensitivity detection of biomarkers or pathogens.

摘要

侧向流动分析(LFA)已被广泛用于现场快速检测分析物,甚至可能是在复杂介质中。然而,基于标准金纳米颗粒的LFA缺乏灵敏度,无法高精度地进行定量测量。为了克服这些局限性,我们将掺镧系元素的纳米颗粒(YVO:Eu 40%)作为新型发光LFA探针进行成像,使用与智能手机相连的自制读数器,并提出了一种原始图像分析方法,可对测试带信号的形状进行条带定量分析。该方法用于检测葡萄球菌肠毒素SEA、SEG、SEH和SEI。与基于金纳米颗粒的先进LFA进行的系统比较表明,分析灵敏度提高了至少一个数量级。我们还提供了两个数量级以上的绝对毒素浓度测量值,并证明了多种毒素的同时定量检测且灵敏度不变。特别是,我们达到的浓度比文献中报道的针对肠毒素的现场多重LFA低100倍。总之,这些结果突出表明,我们基于发光纳米颗粒的方法提供了一个强大且通用的现场框架,用于检测多种生物分子,其灵敏度接近酶联免疫吸附测定(ELISA)所获得的灵敏度。这为分析免疫测定领域的范式转变铺平了道路,通过提供对生物标志物或病原体的快速定量高灵敏度检测。

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