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基于DNA酶催化和金纳米棒蚀刻的用于赭曲霉毒素A检测的高效多色视觉生物传感器。

Effective multicolor visual biosensor for ochratoxin A detection enabled by DNAzyme catalysis and gold nanorod etching.

作者信息

Guo Zhiqiang, Zhang Mingshuo, Zhang Haiping, Ren Xinru, Xiao Yijing, Sun Weiqing, Wang Yu, Liu Su, Huang Jiadong

机构信息

Key Laboratory of Chemical Sensing & Analysis in Universities of Shandong, School of Chemistry and Chemical Engineering, University of Jinan, Jinan, 250022, People's Republic of China.

School of Water Conservancy and Environment, University of Jinan, Jinan, 250022, People's Republic of China.

出版信息

Mikrochim Acta. 2024 Dec 26;192(1):33. doi: 10.1007/s00604-024-06883-3.

Abstract

A novel detection technique is introduced that offers sensitive and reliable ochratoxin A (OTA) detection. The method leverages the etching of gold nanorods (AuNRs) stabilized by hexadecyl trimethyl ammonium bromide (CTAB) using the oxidized form of 3,3',5,5'-tetramethyl benzidine sulfate (TMB), creating a susceptible multicolor visual detection system for OTA. The visual detection is enabled by Mg-assisted DNAzyme catalysis combined with the catalytic hairpin assembly (CHA) signal amplification strategy. The presence of OTA triggers CHA and signaling responses along with the formation of G-quadruplex-hemin DNAzyme, which promotes the oxidation of TMB with HO, leading to the etching of AuNRs and a reduction in their aspect ratio. AuNRs experienced a blue shift in the longitudinal localized surface plasmon resonance peak, resulting in a color change. The technique has been shown to detect OTA with a low detection limit of 0.309 pg/mL, demonstrating high sensitivity and specificity. The detection technique offers versatility by enabling the detection of other pollutants through a simple replacement of the aptamer, expanding the range of detection platforms available for pollutant determinations.

摘要

介绍了一种新型检测技术,该技术可实现对赭曲霉毒素A(OTA)的灵敏且可靠的检测。该方法利用3,3',5,5'-四甲基联苯胺硫酸盐(TMB)的氧化形式蚀刻由十六烷基三甲基溴化铵(CTAB)稳定的金纳米棒(AuNRs),从而创建了一种用于OTA的灵敏多色视觉检测系统。视觉检测通过镁辅助的DNAzyme催化与催化发夹组装(CHA)信号放大策略相结合来实现。OTA的存在会触发CHA和信号响应,同时形成G-四链体-血红素DNAzyme,其促进TMB与HO的氧化反应,导致AuNRs被蚀刻并使其纵横比降低。AuNRs的纵向局部表面等离子体共振峰发生蓝移,从而导致颜色变化。该技术已被证明能够以0.309 pg/mL的低检测限检测OTA,具有高灵敏度和特异性。该检测技术具有通用性,通过简单更换适配体即可检测其他污染物,从而扩大了可用于污染物测定的检测平台范围。

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