平行稀释微流控装置,用于分子诊断中对数浓度的产生

IF 5.4 2区 工程技术 Q1 BIOCHEMICAL RESEARCH METHODS
Lab on a Chip Pub Date : 2025-06-04 DOI:10.1039/D5LC00356C
Akira Miyajima, Fumiya Nishimura, Daigo Natsuhara, Yuka Kiba, Shunya Okamoto, Moeto Nagai, Tadashi Yamamuro, Masashi Kitamura and Takayuki Shibata
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引用次数: 0

摘要

在这项研究中,我们提出了一种遗传诊断设备,具有四步对数稀释能力,可以使用比色环介导等温扩增(LAMP)方法在一次操作中快速可靠地检测目标核酸。一个创新的特点是具有不同微通道高度的汇合点,即使在大体积流量变化(10 - 10,000倍)的情况下,也能确保液体同步流入,同时防止回流。这使得每个稀释因子在恒定压力下独立产生。此外,一个集成的不对称微混合器在层流条件下有效混合两种液体,使混合溶液以均匀浓度同时分配到五个微室中,每个稀释系数。此外,每个微室出口的永久截止阀可防止泄漏,最大限度地减少宝贵样品和试剂的浪费。我们证明,稀释后的样品是准确地准备在预期的对数稀释因子在单一操作中使用纯化的大麻种子DNA,实现检测灵敏度类似于传统的基于浊度的LAMP测定。此外,我们使用粗提取的大麻树脂DNA,其中含有多种基因扩增抑制剂,成功地在一次检测中检测到目标核酸。总的来说,这种多功能设备消除了大量的手工样品制备,并具有在传染病检测,食品安全和非法药物检测等应用中进行现场基因检测的潜力。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Parallel dilution microfluidic device for enabling logarithmic concentration generation in molecular diagnostics†

Parallel dilution microfluidic device for enabling logarithmic concentration generation in molecular diagnostics†

In this study, we present a genetic diagnostic device with a four-stepwise logarithmic dilution capability for rapid and reliable detection of target nucleic acids in a single operation using the colorimetric loop-mediated isothermal amplification (LAMP) method. An innovative feature is the confluent point with differing microchannel heights ensuring the synchronized inflow of liquids while preventing backflow, even under large volumetric flow rate variations (10–10 000-fold). This enabled the independent generation of each dilution factor under constant pressure. Furthermore, an integrated asymmetric micromixer effectively mixed two liquids under laminar flow conditions, enabling simultaneous dispensing of the mixed solution at uniform concentrations into five microchambers for each dilution factor. Additionally, a permanent stop valve in the outlet of each microchamber prevented leakages, minimizing the waste of valuable samples and reagents. We demonstrate that diluted samples were accurately prepared at the intended logarithmic dilution factors in a single operation using purified cannabis seed DNA, achieving detection sensitivity similar to that of conventional turbidity-based LAMP assays. Moreover, we used crudely extracted cannabis resin DNA, which contains several gene amplification inhibitors, successfully detecting the target nucleic acids in a single test. Overall, this versatile device eliminates extensive manual sample preparation and has potential for on-site genetic testing in applications such as infectious disease detection, food safety, and illegal drug testing.

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来源期刊
Lab on a Chip
Lab on a Chip 工程技术-化学综合
CiteScore
11.10
自引率
8.20%
发文量
434
审稿时长
2.6 months
期刊介绍: Lab on a Chip is the premiere journal that publishes cutting-edge research in the field of miniaturization. By their very nature, microfluidic/nanofluidic/miniaturized systems are at the intersection of disciplines, spanning fundamental research to high-end application, which is reflected by the broad readership of the journal. Lab on a Chip publishes two types of papers on original research: full-length research papers and communications. Papers should demonstrate innovations, which can come from technical advancements or applications addressing pressing needs in globally important areas. The journal also publishes Comments, Reviews, and Perspectives.
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