Abstract
There is an ever-growing need for detection methods that are both sensitive and efficient, such that reagent and sample consumption is minimized. Nanopillar arrays offer an attractive option to fill this need by virtue of their small scale in conjunction with their field enhancement intensity gains. This work investigates the use of nanopillar substrates for the detection of the uranyl ion and DNA, two analytes unalike but for their low quantum efficiencies combined with the need for high-throughput analyses. Herein, the adaptability of these platforms was explored, as methods for the successful surface immobilization of both analytes were developed and compared, resulting in a limit of detection for the uranyl ion of less than 1 ppm with a 0.2 μL sample volume. Moreover, differentiation between single-stranded and double-stranded DNA was possible, including qualitative identification between double-stranded DNA and DNA of the same sequence, but with a 10-base-pair mismatch.
Original language | English |
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Pages (from-to) | 7313-7319 |
Number of pages | 7 |
Journal | ACS Omega |
Volume | 2 |
Issue number | 10 |
DOIs | |
State | Published - Oct 31 2017 |
Funding
This material is based upon work supported by the National Science Foundation under grant no. 1144947 with the University of Tennessee, Knoxville. A portion of this research was conducted at the Center for Nanophase Materials Sciences, which is a DOE Office of Science User Facility, as well at the Y-12 National Security Complex. We also acknowledge John R. Dunlap, Ph.D., and the JIAM Microscopy Center and Advanced Microscopy and Imaging Center at UTK for access to facilities.
Funders | Funder number |
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National Science Foundation | |
Directorate for Mathematical and Physical Sciences | 1144947 |
University of Tennessee |