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Gold aggregating gold: A novel nanoparticle biosensor approach for the direct quantification of hepatitis C virus RNA in clinical samples

机译:金聚集金:一种新型纳米粒子生物传感器方法,用于临床样品中丙型肝炎病毒RNa的直接定量

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摘要

The affordable and reliable detection of Hepatitis C Virus (HCV) RNA is a cornerstone in the management andudcontrol of infection, affecting approximately 3% of the global population. However, the existing technologies areudexpensive, labor intensive and time consuming, posing significant limitations to their wide-scale exploitation,udparticularly in economically deprived populations. Here, we utilized the unique optical and physicochemicaludproperties of gold nanoparticles (AuNPs) to develop a novel assay platform shown to be rapid and robust inudsensing and quantifying unamplified HCV RNA in clinical samples. The assay is based on inducing aggregationudof citrate AuNPs decorated with a specific nucleic acid probe. Two types of cationic AuNPs, cysteamine andudCTAB capped, were compared to achieve maximum assay performance. The technology is simple, rapid, costudeffective and quantitative with 93.3% sensitivity, high specificity and detection limit of 4.57 IU/µl. Finally, ouruddata suggest that RNA folding impact the aggregation behavior of the functionalized AuNPs, with broaderudapplications in other nucleic acid detection technologies.
机译:负担得起且可靠的丙型肝炎病毒(HCV)RNA检测是感染管理和控制的基石,约占全球人口的3%。但是,现有技术价格昂贵,劳动强度大且费时,严重限制了它们的大规模开发,尤其是在经济贫困的人口中。在这里,我们利用金纳米颗粒(AuNPs)独特的光学和物理化学性质,开发了一种新颖的检测平台,该平台可快速,可靠地检测和定量临床样品中未扩增的HCV RNA。该测定基于诱导用特异性核酸探针修饰的柠檬酸盐AuNP的聚集/ ud。比较了两种类型的阳离子AuNP(半胱胺和udCTAB封端),以实现最大的检测性能。该技术简单,快速,成本低廉且定量,灵敏度为93.3%,特异性高,检出限为4.57 IU / µl。最后,我们的 uddata提示RNA折叠会影响功能化AuNP的聚集行为,在其他核酸检测技术中具有更广泛的应用。

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