The enhanced diffusional mixing for latex immunoagglutination assay in a microfluidic device
- Authors
- Han, Jin-Hee; Kim, Kye-Seong; Yoon, 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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