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SERS-based immunoassay using a gold array-embedded gradient microfluidic chip

Authors
Lee, MoonkwonLee, KangsunKim, Ki HyungOh, Kwang W.Choo, Jaebum
Issue Date
Aug-2012
Publisher
ROYAL SOC CHEMISTRY
Citation
LAB ON A CHIP, v.12, no.19, pp 3720 - 3727
Pages
8
Journal Title
LAB ON A CHIP
Volume
12
Number
19
Start Page
3720
End Page
3727
URI
https://scholarworks.bwise.kr/cau/handle/2019.sw.cau/45989
DOI
10.1039/c2lc40353f
ISSN
1473-0197
1473-0189
Abstract
Here we report the development of a programmable and fully automatic gold array-embedded gradient microfluidic chip that integrates a gradient microfluidic device with gold-patterned microarray wells. This device provides a convenient and reproducible surface-enhanced Raman scattering (SERS)-based immunoassay platform for cancer biomarkers. We used hollow gold nanospheres (HGNs) as SERS agents because of their highly sensitive and reproducible characteristics. The utility of this platform was demonstrated by the quantitative immunoassay of alpha-fetoprotein (AFP) model protein marker. Our proposed SERS-based immunoassay platform has many advantages over other previously reported SERS immunoassay methods. The tedious manual dilution process of repetitive pipetting and inaccurate dilution is eliminated with this process because various concentrations of biomarker are automatically generated by microfluidic gradient generators with N cascade-mixing stages. The total assay time from serial dilution to SERS detection takes less than 60 min because all of the experimental conditions for the formation and detection of immunocomplexes can be automatically controlled inside the exquisitely designed microfluidic channel. Thus, this novel SERS-based microfluidic assay technique is expected to be a powerful clinical tool for fast and sensitive cancer marker detection.
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자연과학대학 (화학과)
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