Skip to main navigation Skip to search Skip to main content

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

  • Moonkwon Lee
  • , Kangsun Lee
  • , Ki Hyung Kim
  • , Kwang W. Oh
  • , Jaebum Choo
  • Hanyang University
  • SUNY Buffalo

Research output: Contribution to journalArticlepeer-review

121 Scopus citations

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.

Original languageEnglish
Pages (from-to)3720-3727
Number of pages8
JournalLab on a Chip
Volume12
Issue number19
DOIs
StatePublished - Oct 7 2012

Fingerprint

Dive into the research topics of 'SERS-based immunoassay using a gold array-embedded gradient microfluidic chip'. Together they form a unique fingerprint.

Cite this