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首页> 外文期刊>Electrophoresis: The Official Journal of the International Electrophoresis Society >Parallel probing of drug uptake of single cancer cells on a microfluidic device
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Parallel probing of drug uptake of single cancer cells on a microfluidic device

机译:微流体装置上单癌细胞吸毒的平行探测

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摘要

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.
机译:摘要毒性抗药性在癌症患者的治疗过程中经常发展。细胞内药物吸收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调查单细胞水平的药物吸收。在这里,我们开发了一种用于平行探测药物摄取的微流体装置。我们组合V型阀门和蠕动泵送以从前列腺癌细胞(PC3)中选择单个细胞,并在其暴露于药物的单独细胞室中依次将它们置位。在环形反应器中产生六种不同浓度的多柔比星,天然荧光抗癌药物,并在封闭的2个NL体积室中暴露于细胞。在18个平行室中监测每个单个细胞随时间透露根据多柔比星的剂量增加的细胞内荧光强度,以及在孵育2小时后的荧光药物的核定位。本文所提出的技术证明了概念实验的第一系列证明,并且它显示出用于探测单癌细胞的药物敏感性的高潜力。

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