Please use this identifier to cite or link to this item: https://hdl.handle.net/10356/94414
Title: Nanoelectronic detection of triggered secretion of pro-inflammatory cytokines using CMOS compatible silicon nanowires
Authors: Pui, Tze Sian
Agarwal, Ajay
Ye, Feng
Huang, Yinxi
Chen, Peng
Keywords: DRNTU::Engineering::Chemical engineering
Issue Date: 2010
Source: Pui, T.-S., Agarwal, A., Ye, F., Huang, Y. & Chen, P. (2011) Nanoelectronic Detection of Triggered Secretion of Pro-inflammatory Cytokines Using CMOS Compatible Silicon Nanowires. Biosensors and Bioelectronics, 26(5), 2746-2750.
Series/Report no.: Biosensors & bioelectronics
Abstract: Nanotechnology, such as nanoelectronic biosensors, is bringing new opportunities and tools to the studies of cell biology, clinical applications, and drug discovery. In this study, cyrstalline silicon nanowire based field-effect transistors fabricated using top-down approach were employed to parallelly detect pro-inflammatory cytokines in the complex biological fluids (cell culture medium and blood samples) with high specificity and femtomolar sensitivity. Using this technique, the dynamic secretion of TNFalpha and IL6 was revealed during the immune response of macrophages and rats to the stimulation of bacteria endotoxin. This technique could provide a unique platform to examine the profile of complex immune responses for fundamental studies and diagnosis.
URI: https://hdl.handle.net/10356/94414
http://hdl.handle.net/10220/7493
ISSN: 0956-5663
DOI: http://dx.doi.org/10.1016/j.bios.2010.09.059
Rights: © 2010 Elsevier B.V.  This is the author created version of a work that has been peer reviewed and accepted for publication by Biosensors and Bioelectronics, Elsevier B.V.  It incorporates referee’s comments but changes resulting from the publishing process, such as copyediting, structural formatting, may not be reflected in this document.  The published version is available at: [DOI: http://dx.doi.org/10.1016/j.bios.2010.09.059 ]
metadata.item.grantfulltext: open
metadata.item.fulltext: With Fulltext
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