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基于非硫醇化核酸功能化金纳米粒子的适体侧向流检测法快速检测卡那霉素。

Non-thiolated nucleic acid functionalized gold nanoparticle-based aptamer lateral flow assay for rapid detection of kanamycin.

机构信息

State Key Laboratory of Food Science and Technology, Jiangnan University, Lihu Road 1800, Wuxi, 214122, People's Republic of China.

School of Food Science and Technology, Jiangnan University, Lihu Road 1800, Wuxi, 214122, People's Republic of China.

出版信息

Mikrochim Acta. 2022 Jun 8;189(7):244. doi: 10.1007/s00604-022-05342-1.

Abstract

A novel Apt-LFA has been established for kanamycin based on non-thiolated nucleic acid-modified colloidal gold nanoprobe (AuNPs@polyA-DNA). The improvement in nucleic acid hybridization speed and efficiency was verified by modifying AuNPs with polyA-DNA strands instead of thiolated oligonucleotides (SH-DNA) strands. Moreover, the AuNPs@polyA-DNA was explored to apply in an Apt-LFA. The experimental factors including the concentration of the aptamer, the concentration of SA-DNA conjugate, the incubation time, and temperature were carefully investigated. In addition, the kanamycin aptamer was modified by extending several bases at its end to modulate the hybridization complementary strand, which was found to significantly improve the performance of Apt-LFA. Under optimal experimental conditions, the Apt-LFA can detect kanamycin in honey with a LOD of 250 ng mL by the naked eyes. A linear range of 50-1250 ng mL was obtained with a LOD of 15 ng mL in honey by a portable reader. The Apt-LFA was successfully applied to the detection of kanamycin in honey with recoveries of 95.1-105.2%.

摘要

建立了一种基于非硫代核酸修饰胶体金纳米探针 (AuNPs@polyA-DNA) 的新型适体侧向流动分析 (Apt-LFA) 用于检测卡那霉素。通过用 polyA-DNA 链而不是硫代寡核苷酸 (SH-DNA) 链修饰 AuNPs,验证了核酸杂交速度和效率的提高。此外,还研究了 AuNPs@polyA-DNA 在 Apt-LFA 中的应用。仔细研究了实验因素,包括适体的浓度、SA-DNA 缀合物的浓度、孵育时间和温度。此外,通过在适体的末端延伸几个碱基来修饰卡那霉素适体,以调节杂交互补链,这被发现显著提高了 Apt-LFA 的性能。在最佳实验条件下,通过肉眼观察,Apt-LFA 可以在蜂蜜中检测到浓度为 250ng mL 的卡那霉素,LOD 为 15ng mL。通过便携式读取器,在蜂蜜中可以获得 50-1250ng mL 的线性范围,LOD 为 15ng mL。该 Apt-LFA 成功应用于蜂蜜中卡那霉素的检测,回收率为 95.1-105.2%。

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