一种用于微流控装置中数字环路介导等温扩增的高速顺序液体分区方法

IF 5.4 2区 工程技术 Q1 BIOCHEMICAL RESEARCH METHODS
Lab on a Chip Pub Date : 2025-07-31 DOI:10.1039/D5LC00486A
Riku Honda, Taketo Saruwatari, Daigo Natsuhara, Yuka Kiba, Shunya Okamoto, Moeto Nagai, Masashi Kitamura and Takayuki Shibata
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引用次数: 0

摘要

准确和快速地定量核酸靶点对于分子诊断至关重要,特别是在资源有限的环境中,需要简单而可靠的技术。本研究提出了一种高通量数字环介导等温扩增(dLAMP)平台,用于样品中核酸的绝对定量,该平台使用由10000纳升级反应微室组成的微流控装置。这种基于聚二甲基硅氧烷(PDMS)的装置使用电子移液器在60秒内完成了一次完全的液体区隔,而不需要表面改性、预脱气、预抽吸或外部泵送系统,而传统方法通常需要这些系统。使用氟化油可靠地分隔了水样/试剂混合物,97%的微室成功填充到其设计体积的至少80%,表现出出色的体积均匀性(CV = 0.07)。针对沙门氏菌和大麻的荧光LAMP检测显示,估计的DNA浓度和真实的DNA浓度之间存在很强的相关性(R²>;0.98),尽管量化一直被低估。合成沙门氏菌和大麻DNA分别需要1000和10000个校正因子,而大麻种子衍生DNA只需要10个校正因子,这表明这些差异是由于LAMP测定的内在性能而不是设备限制造成的。dLAMP装置还能够在10 ng µL毒血症中成功检测大麻种子DNA,这抑制了传统的基于浊度的LAMP扩增,证明了它在即时检测(POCT)应用中的稳定期。移液器操作的dLAMP平台独特的分区策略可在不影响操作简单性的情况下实现高可扩展性,实现高通量,宽动态范围和准确定量。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

A high-speed sequential liquid compartmentalization method for digital loop-mediated isothermal amplification in a microfluidic device

A high-speed sequential liquid compartmentalization method for digital loop-mediated isothermal amplification in a microfluidic device

Accurate and rapid quantification of nucleic acid targets is crucial for molecular diagnostics, particularly in resource-limited settings where simple and robust technologies are required. This study presents a high-throughput digital loop-mediated isothermal amplification (dLAMP) platform for the absolute quantification of nucleic acids in a sample, using a microfluidic device comprising ten thousand nanoliter-scale reaction microchambers. The polydimethylsiloxane (PDMS)-based device achieved complete liquid compartmentalization within 60 s in a single operation using an electronic pipette, without requiring surface modification, pre-degassing, pre-priming, or external pumping systems, which are typically necessary in conventional methods. The aqueous sample/reagent mixture was reliably compartmentalized using fluorinated oil, with 97% of the microchambers successfully filled to at least 80% of their designed volume, exhibiting excellent volumetric uniformity (CV = 0.07). Fluorescent LAMP assays targeting Salmonella and cannabis exhibited strong correlations between estimated and true DNA concentrations (R2 > 0.98), although quantification was consistently underestimated. Correction factors of 1000 and 10 000 were required for synthetic Salmonella and cannabis DNA, respectively, whereas only 10 were needed for cannabis seed-derived DNA, indicating these discrepancies were due to the intrinsic performance of the LAMP assays rather than device limitations. The dLAMP device also enabled the successful detection of cannabis seed DNA in the presence of 10 ng μL−1 humic acid, which inhibits amplification in conventional turbidity-based LAMP, demonstrating its robustness for point-of-care testing (POCT) applications. The distinctive compartmentalization strategy of the pipette-operated dLAMP platform enables high scalability without compromising operational simplicity, achieving high throughput, wide dynamic range, and accurate quantification.

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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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