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An Enhanced Lateral Flow Assay Based on Aptamer–Magnetic Separation and Multifold AuNPs for Ultrasensitive Detection of Salmonella Typhimurium in Milk

机译:基于适体 - 磁性分离的增强横向流动测定和用于牛奶中沙门氏菌伤寒沙门氏菌的超敏感检测

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摘要

In this paper, a novel and ultrasensitive lateral flow assay (LFA) based on aptamer–magnetic separation, and multifold Au nanoparticles (AuNPs) was developed for visual detecting Salmonella enterica ser. Typhimurium (S. Typhimurium). The method realized magnetic enrichment and signal transduction via magnetic separation and achieved signal amplification through hybridizing AuNPs–capture probes and AuNPs–amplification probes to form multifold AuNPs. Two different thiolated single-strand DNA (ssDNA) on the AuNPs–capture probe played different roles. One was combined with the AuNPs–amplification probe on the conjugate pad to achieve enhanced signals. The other was connected to transduction ssDNA1 released by aptamer–magnetic capture of S. Typhimurium, and captured by the T-line, forming a positive signal. This method had an excellent linear relationship ranging from 8.6 × 102 CFU/mL to 8.6 × 107 CFU/mL with the limit of detection (LOD) as low as 8.6 × 100 CFU/mL in pure culture. In actual samples, the visual LOD was 4.1 × 102 CFU/mL, which did not carry out nucleic acid amplification and pre-enrichment, increasing three orders of magnitudes than unenhanced assays with single–dose AuNPs and no magnetic separation. Furthermore, the system showed high specificity, having no reaction with other nontarget strains. This visual signal amplificated system would be a potential platform for ultrasensitive monitoring S. Typhimurium in milk samples.
机译:在本文中,基于适体 - 磁性分离的新型和超敏横向流动测定(LFA),并为Visual Distration Salmella肠道Ser开发了基于适体 - 磁性分离和多滤波纳米颗粒(AUNP)。 Typhimurium(触风蕈类)。该方法通过磁分离实现磁性富集和信号转导,并通过杂交AUNPS捕获探针和AUNPS放大探针实现信号放大,以形成多变量的AUNP。 AUNPS捕获探针上的两个不同的硫醇单链DNA(SSDNA)起不同的作用。将一个与共轭垫上的AUNPS放大探针相结合,以实现增强的信号。另一个连接到通过适体 - 磁性捕获的S.鼠脊酮捕获的转导SSDNA1,并由T线捕获,形成正信号。该方法具有优异的线性关系,从8.6×102 cfu / ml到8.6×107 cfu / ml,纯培养中的检测极限(LOD)低至8.6×100cfu / ml。在实际样品中,视觉LOD为4.1×102 CFU / mL,其未进行核酸扩增和预富集,增加三个级比,而不是单剂量肛周且磁性分离。此外,该系统表现出高特异性,没有与其他Nontarget菌株的反应。该视觉信号放大系统将是牛奶样本中超声监测S.鼠癣菌的潜在平台。

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