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The enhanced diffusional mixing for latex immunoagglutination assay in a microfluidic device

Authors
Han, Jin-HeeKim, Kye-SeongYoon, Jeong-Yeol
Issue Date
Feb-2007
Publisher
Elsevier BV
Keywords
latex immunoagglutination assay; diffusional mixing; microfluidic device; non-specific binding
Citation
Analytica Chimica Acta, v.584, no.2, pp 252 - 259
Pages
8
Indexed
SCIE
SCOPUS
Journal Title
Analytica Chimica Acta
Volume
584
Number
2
Start Page
252
End Page
259
URI
https://scholarworks.bwise.kr/hanyang/handle/2021.sw.hanyang/172339
DOI
10.1016/j.aca.2006.11.044
ISSN
0003-2670
1873-4324
Abstract
Latex immunoagglutination assay in a microfluidic device is expected to be even easier than its large-sized, commercialized counterpart. However, such demonstration has had a limited success due to the difficulties in mixing in a microfluidic device, especially for the microparticles used in latex immunoagglutination assay. The primary goal of this work is to improve diffusional mixing towards the successful latex immunoagglutination in a microfluidic devices without any non-specific binding. To this end, SDS (sodium dodecyl sulfate, an ionic surfactant) or Tween 80 (polyethylene sorbitol ester, a non-ionic surfactant) was added to the antibody-conjugated polystyrene (PS) microparticle suspension. These surfactant-added particle suspensions were mixed with the target antigen solution at the Y-junction of a microfluidic device. The immunoagglutination and the diffusion behavior were visually identified with an inverted light microscope. Both surfactants showed some problems such as non-specific binding (with SDS) or very poor diffusion (with Tween 80). As an alternative approach, therefore, highly carboxylated PS microparticles, where the surface is saturated with carboxyl-terminated side chains, were evaluated without using any surfactants. These particles showed very low non-specific binding comparable to that with Tween 80 and good diffusional mixing equivalent to that with SIDS. (c) 2006 Elsevier B.V. All rights reserved.
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