用于复杂流体基质中增强核酸分析的水凝胶珠

IF 5.4 2区 工程技术 Q1 BIOCHEMICAL RESEARCH METHODS
Lab on a Chip Pub Date : 2025-07-08 DOI:10.1039/D5LC00447K
Lokman Alpsoy, Stephan Tieu, Sina Dehestanizad, Thomas Brandstetter and Jürgen Rühe
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引用次数: 0

摘要

我们提出了一种功能化的水凝胶珠平台,旨在捕获从肿瘤细胞释放到血液中的游离DNA (cfDNA),并将这种cfDNA用作癌症检测的生物标志物。在两相微流体系统中,通过光交联制备了带有共价探针(HBP)的水凝胶珠。产生微球的前体溶液由光反应共聚物、磁性纳米颗粒、作为微球识别条形码的cy3标记的寡核苷酸和用于结合目标DNA的特定探针组成。这些溶液在微流体系统中产生液滴,并通过C, h插入交联(CHic)进行光交联。作为示范案例,水凝胶珠用于检测MCF-7细胞中的突变(c.1633G> a),已知该突变通过激活致癌信号通路促进乳腺癌进展。利用荧光读取器成功地检测了磷酸盐缓冲盐水(PBS)、血清和全血中荧光标记的突变序列(92 bp),然后通过聚合酶链反应(PCR)进行扩增。所述cfDNA检测方法的灵敏度低至0.36 ng/mL,低于目前文献报道的检出限。由于含有捕获的DNA的水凝胶珠可以直接进行PCR扩增目标序列,而无需任何额外的纯化步骤,因此可以进一步增强水凝胶珠平台的灵敏度。生产、修饰和功能化水凝胶珠的简单性,加上它们在检测cfDNA方面的高灵敏度,使该平台成为诊断一系列疾病的有希望的方法。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Hydrogel beads for enhanced nucleic acid analysis in complex fluid matrices†

Hydrogel beads for enhanced nucleic acid analysis in complex fluid matrices†

We present a functionalized hydrogel bead platform designed to capture cell-free DNA (cfDNA), which is released from tumor cells into the bloodstream, and the use of this cfDNA as a biomarker for cancer detection. Hydrogel beads with covalently incorporated probes (HBP) are generated via photo-cross-linking in a two-phase microfluidic system. The precursor solutions from which the beads are generated are comprised of a photoreactive copolymer, magnetic nanoparticles, Cy3-labelled oligonucleotides serving as a barcode for bead identification, and a specific probe designed to bind the target DNA. From these solutions, droplets are generated in the microfluidic system and photocross-linked through C, H-insertion cross-linking (CHic). As a demonstration case, the hydrogel beads are used to detect a mutation (c.1633G>A) in MCF-7 cells, which is known to promote breast cancer progression by activating oncogenic signalling pathways. The HBPs were successfully employed to detect a fluorescently labelled mutation sequence (92 bp) in phosphate-buffered saline (PBS), serum, and whole blood using a fluorescent reader, followed by amplification through polymerase chain reaction (PCR). The sensitivity of the cfDNA detection method described here demonstrates a detection limit as low as 0.36 ng mL−1, which is lower than any other detection limit in the literature so far. The sensitivity of the hydrogel bead platform can be further significantly increased. This is because beads containing the captured DNA can be subjected directly to PCR for the amplification of the target sequence, eliminating the need for any additional purification steps. The simplicity of production, modification, and functionalization of the hydrogel beads, coupled with their high sensitivity in detecting cfDNA, makes this platform a promising approach for diagnosing a range of diseases.

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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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