Bead-based microfluidic immunoassays: The next generation

被引:224
作者
Lim, C. T.
Zhang, Y.
机构
[1] Natl Univ Singapore, Fac Engn, Div Bioengn, Singapore 117576, Singapore
[2] Natl Univ Singapore, Nanosci & Nanotechnol Initiat, Singapore 117576, Singapore
关键词
microfluidics; immunoassays; bead-based assays; encoded microbeads;
D O I
10.1016/j.bios.2006.06.005
中图分类号
Q6 [生物物理学];
学科分类号
071011 [生物物理学];
摘要
Microfluidic devices possess many advantages like high throughput, short analysis time, small volume and high sensitivity that fulfill all the important criteria of an immunoassay used for clinical diagnoses, environmental analyses and biochemical studies. These devices can be made from a few different materials, with polymers presently emerging as the most popular choice. Other than being optically clear, non-toxic and cheap, polymers can also be easily fabricated with a variety of techniques. In addition, there are many polymer surface modification methods available to improve the efficiency of these devices. Unfortunately, current microfluidic immunoassays have limited multiplexing capability compared to flow cytometric assays. Flow cytometry employ the use of encoded microbeads in contrast with normal or paramagnetic microbeads applied in current microfluidic devices. The encoded microbead is the key in providing multiplexing capability to the assay by allowing multi-analyte analysis. Using several unique sets of code, different analytes can be detected in a single assay by tracing the identity of individual beads. The same principle could be applied to microfluidic immunoassays in order to retain all the advantages of a fluidic device and significantly improve multiplexing capability. (c) 2006 Elsevier B.V. All rights reserved.
引用
收藏
页码:1197 / 1204
页数:8
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