TY - GEN
T1 - Automated immunoassay system based on the colorimetric detection
AU - Lei, Kin Fong
PY - 2012
Y1 - 2012
N2 - In this work, an automated immunoassay system is developed based on colorimetric detection for the application of clinical diagnostics. In this system, most of the biological processes of sandwich immunoassay can be performed automatically. The immunoassay result can be represented by color intensity and observed by a regular camera or even naked eye. The biological reactions were performed in a microfluidic chip and the result of sandwich immunoassay could be observed directly. An example of the sandwich immunoassay has been demonstrated using this automated system. Antihuman IgG, human IgG, and anti-human IgG-Biotin conjugates were selected as the primary antibody, target antigen, and secondary antibody, respectively. The target antigen concentration ranging from 0.5 to 160 ng/ml can be detected quantitatively and the detection limit was 0.5 ng/ml. Since the detection method is simplicity, low cost, and miniaturization; therefore, the proposed system has the potential to be developed to an automated disease screening system.
AB - In this work, an automated immunoassay system is developed based on colorimetric detection for the application of clinical diagnostics. In this system, most of the biological processes of sandwich immunoassay can be performed automatically. The immunoassay result can be represented by color intensity and observed by a regular camera or even naked eye. The biological reactions were performed in a microfluidic chip and the result of sandwich immunoassay could be observed directly. An example of the sandwich immunoassay has been demonstrated using this automated system. Antihuman IgG, human IgG, and anti-human IgG-Biotin conjugates were selected as the primary antibody, target antigen, and secondary antibody, respectively. The target antigen concentration ranging from 0.5 to 160 ng/ml can be detected quantitatively and the detection limit was 0.5 ng/ml. Since the detection method is simplicity, low cost, and miniaturization; therefore, the proposed system has the potential to be developed to an automated disease screening system.
KW - Clinical diagnostics
KW - Gold nanoparticles
KW - Microfluidics
KW - Sandwich immunoassay
UR - http://www.scopus.com/inward/record.url?scp=84861569596&partnerID=8YFLogxK
U2 - 10.1109/NEMS.2012.6196758
DO - 10.1109/NEMS.2012.6196758
M3 - 会议稿件
AN - SCOPUS:84861569596
SN - 9781467311243
T3 - 2012 7th IEEE International Conference on Nano/Micro Engineered and Molecular Systems, NEMS 2012
SP - 208
EP - 212
BT - 2012 7th IEEE International Conference on Nano/Micro Engineered and Molecular Systems, NEMS 2012
T2 - 7th IEEE International Conference on Nano/Micro Engineered and Molecular Systems, NEMS 2012
Y2 - 5 March 2012 through 8 March 2012
ER -