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Elsevier, Biosensors and Bioelectronics, 11(23), p. 1749-1753

DOI: 10.1016/j.bios.2008.02.008

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Colorimetric determination of urinary adenosine using aptamer-modified gold nanoparticles

This paper is available in a repository.
This paper is available in a repository.

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Abstract

生醫工程與環境科學系 ; ©2008 Elsevier - This paper describes a colorimetric sensing approach for the determination of adenosine triphosphate (ATP) using aptamer-modified gold nanoparticles (Apt-Au NPs). In the absence of the analytes, the color of the Apt-Au NPs solution changed from wine-red to purple as a result of salt-induced aggregation. Binding of the analytes to the Apt-Au NPs induced folding of the aptamers on the An NP surfaces into four-stranded tetraplex structures (G-quartet) and/or an increase in charge density. As a result, the Apt-Au NPs solution was wine-red in color in the presence of the analytes under high salt conditions. For mixtures of ATP (20.0-100.0 nM), Apt-Au NPs (3.0 nM), 10.0% poly(ethylene glycol), 0.2 mu M TOTO-3, 150.0 mM NaCl, 15.0 mM KCl, and 16.0 mM Tris-HCl (pH 7.4), a linear correlation (R-2 =0.99) existed between the ratio of the extinctions of the Apt-Au NPs at 650 and 520 nm (Ex(650/520)) and the concentration of ATP. The limit of detection for ATP was 10.0 nM. The practicality of this simple, sensitive, specific, and cost-effective approach was demonstrated through the determination of the concentration of adenosine in urine samples.