SERS-based multiple biomarker detection using a gold-patterned microarray chip
- Authors
- Kim, Insup; Junejo, Inam-ur-Rehman; Lee, Moonkwon; Lee, Sangyeop; Lee, Eun Kyu; Chang, Soo-Ik; Choo, Jaebum
- Issue Date
- 12-Sep-2012
- Publisher
- ELSEVIER
- Keywords
- Microarray chip; Hollow gold nanospheres; Surface-enhanced Raman scattering; Multiplex assay; Immunoassay; ELISA
- Citation
- JOURNAL OF MOLECULAR STRUCTURE, v.1023, pp.197 - 203
- Journal Title
- JOURNAL OF MOLECULAR STRUCTURE
- Volume
- 1023
- Start Page
- 197
- End Page
- 203
- URI
- https://scholarworks.bwise.kr/gachon/handle/2020.sw.gachon/16166
- DOI
- 10.1016/j.molstruc.2012.04.031
- ISSN
- 0022-2860
- Abstract
- We report a highly sensitive surface-enhanced Raman scattering (SERS)-based immunoassay platform for the multiplex detection of biomarkers. For this purpose, a gold-patterned microarray chip has been fabricated and used as a SERS detection template. Here, a typical sandwich immunocomplex protocol was adopted. Monoclonal antibodies were immobilized on gold patterned substrates, and then antigen solutions and polyclonal antibody-conjugated hollow gold nanospheres (HGNs) were sequentially added for the formation of sandwich immunocomplexes. Antigen biomarkers can be quantitatively assayed by monitoring the intensity change of a characteristic SERS peak of a reporter molecule adsorbed on the surfaces of HGNs. Under optimized assay conditions, the limits of detections (LODs) were determined to be 10 fg/mL for human IgG and 10-100 fg/mL for rabbit IgG. In addition, the SERS-based immunoassay technique can be applied in a wider dynamic concentration range with a good sensitivity compared to ELISA. The proposed method fulfills the current needs of high sensitivity and selectivity which are essential for the clinical diagnosis of a disease. (c) 2012 Elsevier B.V. All rights reserved.
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