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用于在复杂流体基质中增强核酸分析的水凝胶珠。

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

作者信息

Alpsoy Lokman, Tieu Stephan, Dehestanizad Sina, Brandstetter Thomas, Rühe Jürgen

机构信息

Department of Microsystems Engineering (IMTEK), Chemistry & Physics of Interfaces, University of Freiburg, 79110 Freiburg im Breisgau, Germany.

Freiburg Center for Interactive Materials and Bioinspired Technologies (FIT), University of Freiburg, 79110 Freiburg im Breisgau, Germany.

出版信息

Lab Chip. 2025 Aug 19;25(17):4422-4435. doi: 10.1039/d5lc00447k.

Abstract

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 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, 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.

摘要

我们展示了一种功能化水凝胶珠平台,该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。通过在两相微流控系统中进行光交联,生成了共价结合探针的水凝胶珠(HBP)。生成珠子的前体溶液由光反应性共聚物、磁性纳米颗粒、用作珠子识别条形码的Cy3标记寡核苷酸以及设计用于结合靶DNA的特异性探针组成。从这些溶液中,在微流控系统中产生液滴,并通过C,H插入交联(CHic)进行光交联。作为一个示范案例,水凝胶珠用于检测MCF-7细胞中的一种突变(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。使用荧光读数器,HBP成功用于在磷酸盐缓冲盐水(PBS)、血清和全血中检测荧光标记的突变序列(92 bp),随后通过聚合酶链反应(PCR)进行扩增。此处描述的cfDNA检测方法的灵敏度显示出低至0.36 ng/mL的检测限,这低于迄今为止文献中的任何其他检测限。水凝胶珠平台的灵敏度可以进一步显著提高。这是因为含有捕获DNA的珠子可以直接进行PCR以扩增靶序列,无需任何额外的纯化步骤。水凝胶珠生产、修饰和功能化的简单性,以及它们在检测cfDNA方面的高灵敏度,使该平台成为诊断一系列疾病的有前途的方法。

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