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

被引:6
|
作者
Yang, Yoonsun [1 ]
Le Gac, Severine [2 ]
Terstappen, Leon W. M. M. [1 ]
Rho, Hoon Suk [2 ]
机构
[1] Univ Twente, MIRA Inst Biomed Technol & Tech Med, Med Cell BioPhys Grp, Enschede, Netherlands
[2] Univ Twente, MIRA Inst Biomed Engn & Tech Med, MESA Inst Nanotechnol, Appl Microfluid BioEngn Res Grp, Enschede, Netherlands
关键词
Drug uptake; Microfluidics; Single cell analysis; MULTIDRUG-RESISTANCE; DOXORUBICIN UPTAKE; ARRAY; CULTURE; ACCUMULATION; CYTOMETRY; SYSTEM;
D O I
10.1002/elps.201700351
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
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.
引用
收藏
页码:548 / 556
页数:9
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