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一种基于信号放大技术的灵敏上转换纳米探针,用于药物性肝损伤的实时原位监测。

A sensitive upconverting nanoprobe based on signal amplification technology for real-time in situ monitoring of drug-induced liver injury.

作者信息

Meng Lingchang, Zheng Xian, Zheng Zuguo, Zhao Zhen, Wang Lai, Zhou Ping, Xin Gui-Zhong, Li Ping, Li Hui-Jun

机构信息

State Key Laboratory of Natural Medicines, China Pharmaceutical University, No. 24 Tongjia Lane, Nanjing 210009, China.

出版信息

Nanoscale. 2020 Jul 23;12(28):15325-15335. doi: 10.1039/d0nr01493a.

Abstract

Drug-induced liver injury (DILI) is increasingly recognized as one of the most challenging global health problems. Conventional in vitro detection methods not only lack specificity and sensitivity but also cannot achieve real-time, straightforward visualization of hepatotoxicity in vivo. Liver-specific miR122 has been observed to be a superior and sensitive biomarker for DILI diagnosis. Herein, a sensitive upconverting nanoprobe synthesized with upconversion nanoparticles (UCNPs) and gold nanorods (GNR) was designed to diagnose hepatotoxicity in vivo. After injection, the nanoprobes accumulated in the liver and were activated by miR122, and the signal amplification technology fully yielded luminescent amplification; hence, the detection sensitivity was improved. Because of the high tissue penetration capability of near-infrared light, this nanoprobe can achieve real-time in situ detection, thereby providing a novel technology for precise biological and medical analysis.

摘要

药物性肝损伤(DILI)日益被认为是全球最具挑战性的健康问题之一。传统的体外检测方法不仅缺乏特异性和敏感性,而且无法在体内实现对肝毒性的实时、直观可视化。肝脏特异性miR122已被观察到是DILI诊断的一种优越且敏感的生物标志物。在此,设计了一种由上转换纳米颗粒(UCNPs)和金纳米棒(GNR)合成的灵敏上转换纳米探针,用于体内肝毒性诊断。注射后,纳米探针在肝脏中积累并被miR122激活,信号放大技术充分实现了发光放大;因此,检测灵敏度得到提高。由于近红外光具有高组织穿透能力,这种纳米探针可以实现实时原位检测,从而为精确的生物和医学分析提供了一种新技术。

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