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将链置换扩增技术应用于基于量子点的荧光侧向流检测条,用于 HIV-DNA 的检测。

Applying strand displacement amplification to quantum dots-based fluorescent lateral flow assay strips for HIV-DNA detection.

机构信息

Hubei Collaborative Innovation Center for Advanced Organic Chemical Materials, Ministry-of-Education Key Laboratory for the Synthesis and Application of Organic Functional Molecules & College of Chemistry and Chemical Engineering, Hubei University, Wuhan 430062, China.

Hubei Collaborative Innovation Center for Advanced Organic Chemical Materials, Ministry-of-Education Key Laboratory for the Synthesis and Application of Organic Functional Molecules & College of Chemistry and Chemical Engineering, Hubei University, Wuhan 430062, China.

出版信息

Biosens Bioelectron. 2018 May 15;105:211-217. doi: 10.1016/j.bios.2018.01.039.

Abstract

Up to now, the colloidal gold labeling immunochromatographic test strip is a mature and applicable technology. However, different from the conventional gold nanoparticle, quantum dot (QD) possesses larger specific surface area and better biocompatibility. So, as a novel nanomaterial, QD is capable of assembling more biomolecule which could enhance the sensitivity and accuracy of strips by rationality. Besides, strand displacement amplification was drawn into our test strips in this paper, this assumption made HIV-DNA recycling many times and converting it to plentiful QD-dsDNA (double-stranded deoxyribonucleic acid), where after these nano-structures would be captured by test zone. Meanwhile, the suggested scheme eliminated the hook effect owing to the target drop out of the incorporation on test zone, and any nucleotide sequence or substance which has aptamers can work as the target, such as carcinoembryonic antigen or mycotoxin. This assay realized the detection limit of as low as 0.76 pM (S/N = 3) and the detection range of 1 pM to 10 nM. In the end, we made use of this fluorescent lateral flow assay strips with great reproducibility for detecting HIV-DNA in human serum, that attested this method could be applied to practical application prospectively.

摘要

到目前为止,胶体金标记免疫层析试纸条是一种成熟且适用的技术。然而,与传统的金纳米颗粒不同,量子点 (QD) 具有更大的比表面积和更好的生物相容性。因此,作为一种新型纳米材料,QD 能够组装更多的生物分子,通过合理的设计可以提高试纸条的灵敏度和准确性。此外,本文将链置换扩增引入到我们的测试条中,该假设使得 HIV-DNA 能够多次循环并将其转化为大量的 QD-dsDNA(双链脱氧核糖核酸),这些纳米结构随后被测试区捕获。同时,由于目标物从测试区的结合中脱落,该方案消除了钩状效应,并且任何具有适体的核苷酸序列或物质都可以作为目标物,如癌胚抗原或真菌毒素。该测定法实现了低至 0.76 pM(S/N = 3)的检测限和 1 pM 至 10 nM 的检测范围。最后,我们利用这种具有良好重现性的荧光侧向流动检测试纸条来检测人血清中的 HIV-DNA,证明该方法具有潜在的实际应用前景。

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