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In relation to this article, we declare that there is no conflict of interest.
Publication history
Received October 24, 2024
Accepted February 25, 2025
Available online May 25, 2025
articles This is an Open-Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/bync/3.0) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
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Antioxidant-Capped Gold Nanoparticles for Colorimetric Detection of Kanamycin

Department of Biological Engineering , Konkuk University , Seoul   05029 , Republic of Korea 1R&D Team, ChoiLab Inc. , Seoul   01811 , Republic of Korea 2Department of Biological Engineering, Advanced Materials Program , Konkuk University , Seoul   05029 , Republic of Korea
akdong486@konkuk.ac.kr, sanghlee@konkuk.ac.kr
Korean Journal of Chemical Engineering, May 2025, 42(5), 1099-1107(9)
https://doi.org/10.1007/s11814-025-00432-1

Abstract

 In the development of aptasensors, which are biosensors that use aptamers (short DNA or RNA molecules) to specifi cally 

bind to target molecules, gold nanoparticles (GNPs) have traditionally been synthesized using citric acid. However, citric 

acid-capped GNPs are not optimized for constructing aptasensors. In this study, we aimed to develop a more sensitive, 

selective, and effi cient antioxidant-capped GNP (A-GNP) probe for the colorimetric detection of kanamycin. We assessed 

the performance of A-GNPs synthesized with polyphenols, multi-carboxylic acids, ascorbic acid, and kojic acid, as both 

reducing agents and stabilizers. Among the tested antioxidants, only ascorbic acid and gallic acid mediated the formation 

of A-GNPs at room temperature and these could be optimized to construct aptasensors by functionalizing the A-GNPs with 

poly(adenine)-tailed DNA aptamers (pA-apt). The colorimetric probe using gallic acid-capped GNPs had a limit of detection

for kanamycin of 6.2 nM, which is lower than the 22.0 nM value obtained using citric acid-capped GNPs. Furthermore, 

this aptasensor showed high selectivity for kanamycin, indicating that the A-GNP/pA-apt probe could be applied as a novel 

aptasensor for antibiotic detection in real-world contexts. 

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