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在微流控装置上对单个癌细胞的药物摄取进行平行探测。

Parallel probing of drug uptake of single cancer cells on a microfluidic device.

作者信息

Yang Yoonsun, Le Gac Séverine, Terstappen Leon Wmm, Rho Hoon Suk

机构信息

Medical Cell BioPhysics Group, MIRA Institute for Biomedical Technology and Technical Medicine, University of Twente, The Netherlands.

Applied Microfluidics for BioEngineering Research Group, MESA+ Institute for Nanotechnology, MIRA Institute for Biomedical Engineering and Technical Medicine, University of Twente, The Netherlands.

出版信息

Electrophoresis. 2018 Feb;39(3):548-556. doi: 10.1002/elps.201700351. Epub 2017 Dec 21.

Abstract

Drug resistance is frequently developing during treatment of cancer patients. Intracellular drug uptake is one of the important characteristics to understand mechanism of drug resistance. However, the heterogeneity of cancer cells requires the investigation of drug uptake at the single cell level. Here, we developed a microfluidic device for parallel probing of drug uptake. We combined a v-type valve and peristaltic pumping to select individual cells from a pool of prostate cancer cells (PC3) and place them successively in separate cell chambers in which they were exposed to the drug. Six different concentrations of doxorubicin, a naturally fluorescent anti-cancer drug, were created in loop-shaped reactors and exposed to the cell in closed 2 nL volume chambers. Monitoring every single cell over time in 18 parallel chambers revealed increased intracellular fluorescence intensity according to the dose of doxorubicin, as well as nuclear localization of the fluorescent drug after 2 h of incubation. The herein proposed technology demonstrated a first series of proof of concept experiments and it shows high potential to use for probing drug sensitivity of single cancer cell.

摘要

在癌症患者的治疗过程中,耐药性经常出现。细胞内药物摄取是理解耐药机制的重要特征之一。然而,癌细胞的异质性需要在单细胞水平上研究药物摄取。在此,我们开发了一种用于并行探测药物摄取的微流控装置。我们将一个V型阀和蠕动泵相结合,从前列腺癌细胞(PC3)池中选择单个细胞,并将它们依次放置在单独的细胞腔室中,在这些腔室中细胞会接触到药物。在环形反应器中制备了六种不同浓度的阿霉素(一种天然荧光抗癌药物),并在封闭的2 nL体积腔室中使其与细胞接触。在18个并行腔室中对每个单细胞进行长时间监测,结果显示细胞内荧光强度随阿霉素剂量增加而增强,并且在孵育2小时后荧光药物定位于细胞核。本文提出的技术展示了一系列初步概念验证实验,并且显示出用于探测单个癌细胞药物敏感性的巨大潜力。

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