Evaluation of Biomolecular Metrics in Microphysiological Systems

被引:0
|
作者
Young, C. L. [1 ]
Griffith, L. G. [1 ]
Lauffenburger, D. A. [1 ]
机构
[1] MIT, Dept Biol Engn, Cambridge, MA 02139 USA
关键词
systems biology; xMAP technology; multiplex assays; inflammation; cytokines; organ-on-a-chip; BioMEMS; Microphysiological Systems (MPS); ANTIBODY; PROTEIN; TECHNOLOGIES; IMMUNOASSAY; CHALLENGES; PLATFORMS; ANTIGEN; ASSAY; SERUM;
D O I
暂无
中图分类号
R318 [生物医学工程];
学科分类号
0831 ;
摘要
The emergence of organs-on-a-chip microfabricated devices and integrated microphysiological systems has facilitated study of human physiology in an organ-specific context, enabling the development and validation of predictive models relevant in drug discovery. Quantitative investigations of cytokine profiles and signaling networks across a range of physiological perturbations, in a highly multiplexed fashion, can provide powerful insights into inflammatory processes. Here, we discuss the challenges associated with multiplex suspension arrays and guidelines to improve validation methods. Advancements in these best practices using multiplex technologies are essential for obtaining quantitative measures of signaling networks in disease progression and biomarker-assisted drug development.
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页数:3
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