Label-free high-throughput impedance-activated cell sorting†

IF 6.1 2区 工程技术 Q1 BIOCHEMICAL RESEARCH METHODS Lab on a Chip Pub Date : 2024-09-20 DOI:10.1039/D4LC00487F
Kui Zhang, Ziyang Xia, Yiming Wang, Lisheng Zheng, Baoqing Li and Jiaru Chu
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Abstract

Cell sorting holds broad applications in fields such as early cancer diagnosis, cell differentiation studies, drug screening, and single-cell sequencing. However, achieving high-throughput and high-purity in label-free single-cell sorting is challenging. To overcome this issue, we propose a label-free, high-throughput, and high-accuracy impedance-activated cell sorting system based on impedance detection and dual membrane pumps. Leveraging the low-latency characteristics of FPGA, the system facilitates real-time dual-frequency single-cell impedance detection with high-throughput (5 × 104 cells per s) for HeLa, MDA-MB-231, and Jurkat cells. Furthermore, the system accomplishes low-latency (less than 0.3 ms), label-free, high-throughput (1000 particles per s) and high-accuracy (almost 99%) single-particle sorting using FPGA-based high-precision sort-timing prediction. In experiments with Jurkat and MDA-MB-231 cells, the system achieved a throughput of up to 1000 cells per s, maintaining a pre-sorting purity of 28.57% and increasing post-sorting purity to 97.09%. These findings indicate that our system holds significant potential for applications in label-free, high-throughput cell sorting.

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无标记高通量阻抗激活细胞分拣技术
细胞分拣在早期癌症诊断、细胞分化研究、药物筛选和单细胞测序等领域有着广泛的应用。然而,在无标记单细胞分选中实现高通量和高纯度具有挑战性。为了克服这一问题,我们提出了一种基于阻抗检测和双膜泵的无标记、高通量和高精度阻抗激活细胞分拣系统。利用 FPGA 的低延迟特性,该系统可对 Hela、MDA-MB-231 和 Jurkat 细胞进行高通量(5 × 104 cells/s)的实时双频单细胞阻抗检测。此外,该系统还利用基于 FPGA 的高精度分拣时间预测,实现了低延迟(小于 0.3 毫秒)、无标记、高通量(1,000 颗粒/秒)和高准确度(近 99%)的单颗粒分拣。在对 Jurkat 和 MDA-MB-231 细胞的实验中,该系统实现了高达 1,000 cells/s 的吞吐量,分选前纯度保持在 28.57%,分选后纯度提高到 97.09%。这些研究结果表明,我们的系统在无标记、高通量细胞分选方面具有巨大的应用潜力。
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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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