增强硝酸纤维素膜上核酸的比色检测:诊断和法医学中的前沿应用

Biosensors Pub Date : 2024-09-05 DOI:10.3390/bios14090430
Nidhi Subhashini, Yannick Kerler, Marcus M. Menger, Olga Böhm, Judith Witte, Christian Stadler, Alexander Griberman
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引用次数: 0

摘要

本研究利用特殊的多通道硝酸纤维素膜和 DNA-Gold 结合物,在纸基横向流动检测法上重新引入了一种不含蛋白质的核酸快速检测方法,显著提高了灵敏度,简化了操作步骤,缩短了检测时间,降低了生产成本,并实现了先进的多重检测。首次展示了一种不含蛋白质的基于核酸的横向流动检测(NALFA),其 DNA 检测限为 1 pmol。这种检测方法的总生产时间成功地从目前已知的数天缩短到几小时。方案的简化和加速使该方法在各种应用中更加方便实用。所开发的方法支持多重检测,可同时检测多达六个 DNA 靶标。与传统的线性检测相比,这种多重检测能力是一项重大改进,可在一次检测中提供更全面的诊断潜力。与传统的线路测试相比,该方法大大缩短了运行时间,提高了诊断程序的效率。该检测方法不含蛋白质,最大程度地减少了免疫测定中普遍存在的交叉反应并发症,尤其是在多重检测的情况下。研究还表明,本研究开发的 NALFA 无需扩增,因此不依赖专业技术人员,也不涉及 DNA 提取和 PCR 过程等劳动密集型步骤。总之,本研究为 DNA 或 RNA 检测提供了一个稳健、高效、高灵敏度的平台,解决了文献中记载的当前方法的几个局限性。在灵敏度、成本降低、生产时间和多路复用能力方面的进步标志着一个实质性的改进,在诊断、法医和分子生物学的各种应用中蕴藏着巨大的潜力。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Enhancing Colorimetric Detection of Nucleic Acids on Nitrocellulose Membranes: Cutting-Edge Applications in Diagnostics and Forensics
This study re-introduces a protein-free rapid test method for nucleic acids on paper based lateral flow assays utilizing special multichannel nitrocellulose membranes and DNA-Gold conjugates, achieving significantly enhanced sensitivity, easier protocols, reduced time of detection, reduced costs of production and advanced multiplexing possibilities. A protein-free nucleic acid-based lateral flow assay (NALFA) with a limit of detection of 1 pmol of DNA is shown for the first time. The total production duration of such an assay was successfully reduced from the currently known several days to just a few hours. The simplification and acceleration of the protocol make the method more accessible and practical for various applications. The developed method supports multiplexing, enabling the simultaneous detection of up to six DNA targets. This multiplexing capability is a significant improvement over traditional line tests and offers more comprehensive diagnostic potential in a single assay. The approach significantly reduces the run time compared to traditional line tests, which enhances the efficiency of diagnostic procedures. The protein-free aspect of this assay minimizes the prevalent complications of cross-reactivity in immunoassays especially in cases of multiplexing. It is also demonstrated that the NALFA developed in this study is amplification-free and hence does not rely on specialized technicians, nor does it involve labour-intensive steps like DNA extraction and PCR processes. Overall, this study presents a robust, efficient, and highly sensitive platform for DNA or RNA detection, addressing several limitations of current methods documented in the literature. The advancements in sensitivity, cost reduction, production time, and multiplexing capabilities mark a substantial improvement, holding great potential for various applications in diagnostics, forensics, and molecular biology.
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