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Ultrasmall near-infrared gold nanoclusters for tumor fluorescence imaging in vivo

机译:在体内用于肿瘤荧光成像的超泡近红外金纳米簇

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摘要

In this paper, we explore the possibility of using ultrasmall near-infrared (NIR) gold nanoclusters (AuNCs) as novel contrast imaging agents for tumor fluorescence imaging in vivo. The fluorescence imaging signal of the tail vein administrated AuNCs in living organisms can spectrally be well distinguished from the background with maximum emission wavelength at about 710 nm, and the high photostability of AuNCs promises continuous imaging in vivo. The uptake of AuNCs by the reticuloendothelial system is relatively low in comparison with other nanoparticle-based contrast imaging agents due to their ultrasmall hydrodynamic size (~2.7 nm). Through the body weight change analysis, the results show that the body weight of the mice administrated with AuNCs has not been changed obviously in comparison with that of the control mice injected with PBS. Furthermore, using MDA-MB-45 and Hela tumor xenograft models, in vivo and ex vivo imaging studies show that the ultrasmall NIR AuNCs are able to be highly accumulated in the tumor areas, thanks to the enhanced permeability and retention (EPR) effects. And the tumor-to-background ratio is about 15 for 6 h postinjection. The results indicate that the ultrasmall NIR AuNCs appear as very promising contrast imaging agents for in vivo fluorescence tumor imaging.
机译:在本文中,我们探讨了使用超大近红外(NIR)金纳米簇(AUNC)作为体内肿瘤荧光成像的新型对比度成像剂的可能性。尾静脉在生物体中管理AUNC的荧光成像信号可以很好地与背景区分开,最大发射波长在约710 nm处,AUNCS的高光稳定性有望在体内连续成像。与其他基于纳米颗粒的对比成像剂相比,网状内皮系统对AUNCS的吸收相对较低,这是由于其超肌水体动力学大小(〜2.7 nm)。通过体重变化分析,结果表明,与注入PBS的对照小鼠相比,用AUNCS施用的小鼠的体重显然没有变化。此外,使用MDA-MB-45和HELA肿瘤异种移植模型,体内和体内成像研究表明,由于渗透率和保留效应增强(EPR)效应,超肌NIR AUNCS能够在肿瘤区域高度积累。注射后6小时,肿瘤与背景的比率约为15。结果表明,超大NIR AUNCs似乎是体内荧光肿瘤成像的非常有希望的对比度成像剂。

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