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基于光电管的光流控芯片装置,用于无堵塞细胞传输时间测量。

Photocell-Based Optofluidic Device for Clogging-Free Cell Transit Time Measurements.

机构信息

Centre for Nano Science and Technology, Istituto Italiano di Tecnologia, Via Rubattino 81, 20134 Milano, Italy.

Dipartimento di Fisica, Politecnico di Milano, Piazza Leonardo da Vinci 32, 20133 Milano, Italy.

出版信息

Biosensors (Basel). 2024 Mar 24;14(4):154. doi: 10.3390/bios14040154.

DOI:10.3390/bios14040154
PMID:38667147
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11047832/
Abstract

Measuring the transit time of a cell forced through a bottleneck is one of the most widely used techniques for the study of cell deformability in flow. It in turn provides an accessible and rapid way of obtaining crucial information regarding cell physiology. Many techniques are currently being investigated to reliably retrieve this time, but their translation to diagnostic-oriented devices is often hampered by their complexity, lack of robustness, and the bulky external equipment required. Herein, we demonstrate the benefits of coupling microfluidics with an optical method, like photocells, to measure the transit time. We exploit the femtosecond laser irradiation followed by chemical etching (FLICE) fabrication technique to build a monolithic 3D device capable of detecting cells flowing through a 3D non-deformable constriction which is fully buried in a fused silica substrate. We validated our chip by measuring the transit times of pristine breast cancer cells (MCF-7) and MCF-7 cells treated with Latrunculin A, a drug typically used to increase their deformability. A difference in transit times can be assessed without the need for complex external instrumentation and/or demanding computational efforts. The high throughput (4000-10,000 cells/min), ease of use, and clogging-free operation of our device bring this approach much closer to real scenarios.

摘要

测量细胞通过瓶颈的传输时间是研究流动中细胞可变形性最广泛使用的技术之一。它反过来为获取有关细胞生理学的关键信息提供了一种便捷快速的方法。目前正在研究许多技术来可靠地获取此时间,但由于其复杂性、缺乏稳健性以及所需的大型外部设备,它们通常难以转化为面向诊断的设备。在这里,我们展示了将微流控与像光电管这样的光学方法相结合来测量传输时间的优势。我们利用飞秒激光照射后化学蚀刻(FLICE)制造技术来构建一个单片 3D 设备,该设备能够检测流过 3D 不可变形收缩的细胞,而该收缩完全埋在熔融石英基板中。我们通过测量原始乳腺癌细胞(MCF-7)和用拉曲库林 A 处理的 MCF-7 细胞的传输时间来验证我们的芯片,拉曲库林 A 是一种通常用于增加其可变形性的药物。可以在不需要复杂的外部仪器和/或苛刻的计算工作的情况下评估传输时间的差异。我们的设备具有高吞吐量(4000-10000 个细胞/分钟)、易于使用和无堵塞操作的特点,使这种方法更接近实际情况。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/79dd/11047832/8855bd61812c/biosensors-14-00154-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/79dd/11047832/2137ae637c83/biosensors-14-00154-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/79dd/11047832/36179181510e/biosensors-14-00154-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/79dd/11047832/dad9aced1a20/biosensors-14-00154-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/79dd/11047832/57572a9da063/biosensors-14-00154-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/79dd/11047832/8855bd61812c/biosensors-14-00154-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/79dd/11047832/2137ae637c83/biosensors-14-00154-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/79dd/11047832/36179181510e/biosensors-14-00154-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/79dd/11047832/dad9aced1a20/biosensors-14-00154-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/79dd/11047832/57572a9da063/biosensors-14-00154-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/79dd/11047832/8855bd61812c/biosensors-14-00154-g005.jpg

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