TY - JOUR
T1 - The enhanced diffusional mixing for latex immunoagglutination assay in a microfluidic device
AU - Han, Jin Hee
AU - Kim, Kye Seong
AU - Yoon, Jeong Yeol
N1 - Funding Information:
The authors thank Dr. Srini Raghavan in Department of Materials Science and Engineering at the University of Arizona for discussion and help in Doppler electrophoretic light scattering. Mr. Lonnie J. Lucas in Department of Agricultural and Biosystems Engineering at the University of Arizona helped in preparing immunoagglutination assay. The authors are grateful to the University of Arizona for the cleanroom facility and subsequent equipment assistance. The funding for this research was provided by the U.S. National Science Foundation (NSF), Award no. EEC-0600855 and by the Faculty Small Grants Program from the University of Arizona Foundation and the Office of the Vice President for Research, Graduate Studies, and Economic Development.
PY - 2007/2/19
Y1 - 2007/2/19
N2 - 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 SDS.
AB - 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 SDS.
KW - Diffusional mixing
KW - Latex immunoagglutination assay
KW - Microfluidic device
KW - Non-specific binding
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U2 - 10.1016/j.aca.2006.11.044
DO - 10.1016/j.aca.2006.11.044
M3 - Article
C2 - 17386612
AN - SCOPUS:33846548080
SN - 0003-2670
VL - 584
SP - 252
EP - 259
JO - Analytica Chimica Acta
JF - Analytica Chimica Acta
IS - 2
ER -