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Nanoslit membrane-integrated fluidic chip for protein detection based on size-dependent particle trapping

Authors
Koh, YulKang, HomanLee, Seung HyunYang, Jin-KyoungKim, Jong-HoLee, Yoon-SikKim, Yong-Kweon
Issue Date
2014
Publisher
ROYAL SOC CHEMISTRY
Keywords
ANODIC ALUMINUM-OXIDE; AGGLUTINATION ASSAY; DEVICE; BEAD; FABRICATION; ENHANCED RAMAN-SCATTERING; POLYMER NANOCHANNELS; IMMUNOASSAY; MAGNETIC NANOPARTICLES; GOLD NANOSPHERES
Citation
LAB ON A CHIP, v.14, no.1, pp.237 - 243
Indexed
SCIE
SCOPUS
Journal Title
LAB ON A CHIP
Volume
14
Number
1
Start Page
237
End Page
243
URI
https://scholarworks.bwise.kr/erica/handle/2021.sw.erica/25884
DOI
10.1039/c3lc50922b
ISSN
1473-0197
Abstract
This paper describes the fabrication of a nanoslit membrane-integrated fluidic chip (Nanoslit-Chip) used for trapping and concentrating micro-/nano-particles of desired size and its application in detecting biological molecules based on target-induced particle aggregation. To trap particles of a specific size, a large scale uniform sized nanoslit fluid channel array is fabricated on a silicon dioxide membrane. A small number of fluorescence labeled particles in a large volume of solution are concentrated into a monolayer of particles in a small nanoslit membrane, which enables us to effectively quantify them via fluorescence intensity. In addition, the particles of desired size (1.8 mu m) are readily separated from the mixture of particles with a different size (450 nm) in Nanoslit-Chip size, and then quantified via fluorescence measurements. Finally, the Nanoslit-Chip is successfully applied to the sensitive detection of proteins by target-induced particle aggregation, trapping, and quantification. This shows its potential as a biological and clinical device for quantitative and sensitive detection of biological molecules.
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Kim, Jong-Ho
ERICA 공학대학 (DEPARTMENT OF MATERIALS SCIENCE AND CHEMICAL ENGINEERING)
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