Automated Reagent-Dispensing System for Microfluidic Cell Biology Assays

被引:8
|
作者
Ly, Jimmy [1 ,2 ]
Masterman-Smith, Michael [1 ]
Ramakrishnan, Ravichandran [1 ,2 ]
Sun, Jing [2 ,3 ]
Kokubun, Brent [1 ]
van Dam, R. Michael [1 ,2 ,3 ]
机构
[1] Univ Calif Los Angeles, Samueli Sch Engn & Appl Sci, Dept Bioengn, Los Angeles, CA USA
[2] Univ Calif Los Angeles, Crump Inst Mol Imaging, Los Angeles, CA USA
[3] Univ Calif Los Angeles, David Geffen Sch Med, Dept Mol & Med Pharmacol, Los Angeles, CA 90095 USA
来源
JALA | 2013年 / 18卷 / 06期
关键词
automated biology; robotics and instrumentation; microfluidics; lab-on-a-chip; HTS; high-throughput screening; CULTURE; DEVICE;
D O I
10.1177/2211068213504758
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Microscale systems that enable measurements of oncological phenomena at the single-cell level have a great capacity to improve therapeutic strategies and diagnostics. Such measurements can reveal unprecedented insights into cellular heterogeneity and its implications into the progression and treatment of complicated cellular disease processes such as those found in cancer. We describe a novel fluid-delivery platform to interface with low-cost microfluidic chips containing arrays of microchambers. Using multiple pairs of needles to aspirate and dispense reagents, the platform enables automated coating of chambers, loading of cells, and treatment with growth media or other agents (e.g., drugs, fixatives, membrane permeabilizers, washes, stains, etc.). The chips can be quantitatively assayed using standard fluorescence-based immunocytochemistry, microscopy, and image analysis tools, to determine, for example, drug response based on differences in protein expression and/or activation of cellular targets on an individual-cell level. In general, automation of fluid and cell handling increases repeatability, eliminates human error, and enables increased throughput, especially for sophisticated, multistep assays such as multiparameter quantitative immunocytochemistry. We report the design of the automated platform and compare several aspects of its performance to manually-loaded microfluidic chips.
引用
收藏
页码:530 / 541
页数:12
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