Full Paper
Quantum-Dot-Tagged Bioresponsive Hydrogel Suspension Array for Multiplex Label-Free DNA Detection
Article first published online: 22 FEB 2010
DOI: 10.1002/adfm.200901812
Copyright © 2010 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim
Additional Information
How to Cite
Zhao, Y., Zhao, X., Tang, B., Xu, W., Li, J., Hu, J. and Gu, Z. (2010), Quantum-Dot-Tagged Bioresponsive Hydrogel Suspension Array for Multiplex Label-Free DNA Detection. Adv. Funct. Mater., 20: 976–982. doi: 10.1002/adfm.200901812
Publication History
- Issue published online: 22 MAR 2010
- Article first published online: 22 FEB 2010
- Manuscript Revised: 24 NOV 2009
- Manuscript Received: 25 SEP 2009
Funded by
- 333 Talent Project Foundation and Qing Lan Project of Jiangsu Province
- Jiangsu Science and Technology Department. Grant Numbers: BE 2009148, BE 2008318
- National Science Foundation of China. Grant Number: 20703010
- Abstract
- Article
- References
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Keywords:
- hydrogels;
- label-free detection;
- quantum dots;
- photonic crystals;
- multiplex assays
Abstract
A novel hydrogel suspension array, which possesses the joint advantages of quantum-dot-encoded technology, bioresponsive hydrogels, and photonic crystal sensors with full multiplexing label-free DNA detection capability is developed. The microcarriers of the suspension array are quantum-dot-tagged DNA-responsive hydrogel photonic beads. In the case of label-free DNA detection, specific hybridization of target DNA and the crosslinked single-stranded DNA in the hydrogel grid will cause hydrogel shrinking, which can be detected as a corresponding blue shift in the Bragg diffraction peak position of the beads that can be used for quantitatively estimating the amount of target DNA. The results of the label-free DNA detection show that the suspension array has high selectivity and sensitivity with a detection limit of 10−9 M. This method has the potential to provide low cost, miniaturization, and simple and real-time monitoring of hybridization reaction platforms for detecting genetic variations and sequencing genes.

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