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用于药物诱导的器官损伤产生的内源性过氧化氢的活体比率成像的荧光纳米探针。

Fluorescent nanoprobe for in-vivo ratiometric imaging of endogenous hydrogen peroxide resulted from drug-induced organ damages.

机构信息

College of Materials Science & Engineering, State Key Laboratory of Luminescent Materials & Devices, South China University of Technology, Guangzhou 510640, China.

College of Materials & Energy, South China Agricultural University, Guangzhou 510642, China.

出版信息

Biosens Bioelectron. 2017 Aug 15;94:278-285. doi: 10.1016/j.bios.2017.03.003. Epub 2017 Mar 6.

DOI:10.1016/j.bios.2017.03.003
PMID:28292734
Abstract

Drug-induced organ damages have been considered as a grave problem regarding public health; hence effective method for in vivo detection of drug-induced organ damages is of great significance. Herein we developed a ratiometric fluorescent nanoprobe (NPs-A), which was prepared by loading the probe molecules into phospholipid bilayer, for assaying hydrogen peroxide (HO, an organ damage biomarker) level in vivo. The photophysical behavior of the probe molecule depends on the electron-withdrawing ability of the group at the 6- position of anthracene ring, on which the recognition moiety for hydrogen peroxide (dicarbonyl coupled with nitrophenyl, referred to as nitrophenyl-dicarbonyl) was introduced. Upon the reaction of the probe with HO, nitrophenyl-dicarbonyl group transforms into carboxyl group, and due to the variation of the electron-withdrawing ability of the 6th substituent, the fluorescent properties of the probe molecule alters accordingly, thus ensuring the ratiometric detection for HO with high selectivity with the detection limit of 0.49μM. In addition, the nanoprobe (NPs-A) was applied for cell and in vivo imaging applications; and the results indicate that it can detect and track the level of HO in living cells and to monitor and spatially map endogenous HO levels in a drug-induced organ damage model of zebrafish.

摘要

药物引起的器官损伤被认为是一个严重的公共卫生问题;因此,用于体内检测药物引起的器官损伤的有效方法具有重要意义。在这里,我们开发了一种比率荧光纳米探针(NPs-A),它是通过将探针分子装载到磷脂双层中来制备的,用于检测体内的过氧化氢(HO,一种器官损伤生物标志物)水平。探针分子的光物理行为取决于蒽环 6 位取代基的吸电子能力,在该位置引入了对过氧化氢的识别部分(二羰基与硝基苯基偶联,称为硝基二羰基)。当探针与 HO 反应时,硝基二羰基基团转化为羧基基团,由于 6 位取代基的吸电子能力发生变化,探针分子的荧光性质相应改变,从而确保了对 HO 的高选择性比率检测,检测限为 0.49μM。此外,该纳米探针(NPs-A)还应用于细胞和体内成像应用;结果表明,它可以检测和跟踪活细胞中 HO 的水平,并在斑马鱼药物诱导的器官损伤模型中监测和空间映射内源性 HO 水平。