首页> 外文期刊>Biosensors & Bioelectronics: The International Journal for the Professional Involved with Research, Technology and Applications of Biosensers and Related Devices >An ultrasensitive alloyed near-infrared quinternary quantum dot-molecular beacon nanodiagnostic bioprobe for influenza virus RNA
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An ultrasensitive alloyed near-infrared quinternary quantum dot-molecular beacon nanodiagnostic bioprobe for influenza virus RNA

机译:流感病毒RNA超敏合金近红外五元量子点信标纳米诊断生物探针

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摘要

Conventional techniques used to diagnose influenza virus face several challenges, such as low sensitivity, slow detection, false positive results and misinterpreted data. Hence, diagnostic probes that can offer robust detection qualities, such as high sensitivity, rapid detection, elimination of false positive data, and specificity for influenza virus, are urgently needed. The near-infrared (NIR) range is an attractive spectral window due to low photon absorption by biological tissues, hence well-constructed fluorescent biosensors that emit within the NIR window can offer an improved limit of detection (LOD). Here, we demonstrate the use of a newly synthesized NIR quinternary alloyed CdZnSeTeS quantum dots (QDs) as an ultrasensitive fluorescence reporter in a conjugated molecular beacon (MB) assay to detect extremely low concentrations of influenza virus H1N1 RNA. Under optimum conditions, two different strains of influenza virus H1N1 RNA were detected based on fluorescence enhancement signal transduction. We successfully discriminated between two different strains of influenza virus H1N1 RNA based on the number of complementary nucleotide base pairs of the MB to the target RNA sequence. The merits of our bioprobe system are rapid detection, high sensitivity (detects H1N1 viral RNA down to 2 copies/mL), specificity and versatility (detects H1N1 viral RNA in human serum). For comparison, a conventional CdSe/ZnS-MB probe could not detect the extremely low concentrations of H1N1 viral RNA detected by our NIR alloyed CdZnSeTeS-MB probe. Our bioprobe detection system produced a LOD as low as similar to 1 copy/mL and is more sensitive than conventional molecular tests and rapid influenza detection tests (RIDTS) probes. (C) 2016 Elsevier B.V. All rights reserved.
机译:用于诊断流感病毒的常规技术面临许多挑战,例如灵敏度低,检测速度慢,假阳性结果和数据解释错误。因此,迫切需要能够提供可靠检测质量的诊断探针,例如高灵敏度,快速检测,消除假阳性数据以及对流感病毒的特异性。由于生物组织的低光子吸收,近红外(NIR)范围是一个有吸引力的光谱窗口,因此在NIR窗口内发射的结构良好的荧光生物传感器可以提供更高的检测极限(LOD)。在这里,我们证明了在共轭分子信标(MB)分析中使用新合成的NIR五元合金化CdZnSeTeS量子点(QDs)作为超灵敏荧光报告分子,可检测极低浓度的流感病毒H1N1 RNA。在最佳条件下,基于荧光增强信号转导,检测到两种不同的流感病毒H1N1 RNA株。我们根据MB与目标RNA序列的互补核苷酸碱基对的数量成功区分了两种不同的流感病毒H1N1 RNA株。我们的生物探针系统的优点是快速检测,高灵敏度(检测低至2拷贝/ mL的H1N1病毒RNA),特异性和多功能性(检测人血清中的H1N1病毒RNA)。为了进行比较,传统的CdSe / ZnS-MB探针无法检测到由我们的NIR合金化CdZnSeTeS-MB探针检测到的极低浓度的H1N1病毒RNA。我们的生物探针检测系​​统产生的LOD低至接近1个拷贝/ mL,并且比常规分子检测和快速流感检测检测(RIDTS)探针灵敏。 (C)2016 Elsevier B.V.保留所有权利。

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