Please use this identifier to cite or link to this item: http://hdl.handle.net/10397/90709
PIRA download icon_1.1View/Download Full Text
Title: Nanomaterials for colorimetric DNA detection
Authors: Lee, T 
Issue Date: 2017
Source: IAS Focused Program: DNA Nanotechnology and Smart Sensors, 19-23 Mar 2017, the Hong Kong University of Science and Technology, Hong Kong (Abstract)
Abstract: Nucleic acid testing is now widely accepted to be the gold standard for pathogen detection in a broad spectrum of applications, including medical diagnostics, food safety monitoring, and environmental surveillance. These assays are virtually performed in resource-rich clinical/central laboratories due to the use of expensive, bulky, and sophisticated equipment. The ability to achieve point-of-care/field testing can provide more timely treatment/response decision. Colorimetric detection is one of the promising technologies in view of its simple signal readout (interpretation by the naked eye and quantification by absorbance measurement). Over the past two decades, nanomaterial-based colorimetric probes have received tremendous attention for the detection of specific DNA/RNA sequences. Our team has focused on two types of nanomaterials: (1) gold nanoparticles (AuNPs) and (2) platinum nanoparticles supported on reduced graphene oxide (PtNPs/rGO). For AuNPs (unique interparticle distance-dependent optical property: red-shift of surface plasmon resonance absorption band upon particle aggregation), our team developed three assay platforms (oligonucleotide-modified AuNP with a silica reinforcement coating for polymerase chain reaction (PCR); carboxyl-modified AuNP for loop-mediated isothermal amplification (LAMP); and poly(ethylene glycol) and carboxyl co-modified AuNP for LAMP). For PtNPs/rGO (superior peroxidase-like activity), our team developed two assay platforms (π-stacking interaction with single-stranded but not double-stranded DNA as well as salt-induced aggregation for PCR; and pH-dependent activity for LAMP). These assay platforms would enable ultrasensitive, simple, and low-cost nucleic acid testing in decentralized settings.
Rights: Posted with permission of the author.
Appears in Collections:Conference Paper

Files in This Item:
File Description SizeFormat 
a0842-n06_1770.pdf759.45 kBAdobe PDFView/Open
Open Access Information
Status open access
File Version Other Version
Show full item record

Page views

101
Last Week
2
Last month
Citations as of Apr 14, 2024

Downloads

23
Citations as of Apr 14, 2024

Google ScholarTM

Check


Items in DSpace are protected by copyright, with all rights reserved, unless otherwise indicated.