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利用缺氧依赖性菁光笼用于体内精准药物释放。

Harnessing Hypoxia-Dependent Cyanine Photocages for In Vivo Precision Drug Release.

机构信息

Key Laboratory for Advanced Materials and Institute of Fine Chemicals, Feringa Nobel Prize Scientist Joint Research Center, Frontiers Science Center for Materiobiology and Dynamic Chemistry, School of Chemistry and Molecular Engineering, East China University of Science & Technology, Shanghai, 200237, China.

State Key Laboratory of Bioreactor Engineering, East China University of Science and Technology, Shanghai, 200237, P. R. China.

出版信息

Angew Chem Int Ed Engl. 2021 Apr 19;60(17):9553-9561. doi: 10.1002/anie.202017349. Epub 2021 Mar 17.

Abstract

Photocaging holds promise for the precise manipulation of biological events in space and time. However, current near-infrared (NIR) photocages are oxygen-dependent for their photolysis and lack of timely feedback regulation, which has proven to be the major bottleneck for targeted therapy. Herein, we present a hypoxia-dependent photo-activation mechanism of dialkylamine-substituted cyanine (Cy-NH) accompanied by emissive fragments generation, which was validated with retrosynthesis and spectral analysis. For the first time, we have realized the orthogonal manipulation of this hypoxia-dependent photocaging and dual-modal optical signals in living cells and tumor-bearing mice, making a breakthrough in the direct spatiotemporal control and in vivo feedback regulation. This unique photoactivation mechanism overcomes the limitation of hypoxia, which allows site-specific remote control for targeted therapy, and expands the photo-trigger toolbox for on-demand drug release, especially in a physiological context with dual-mode optical imaging under hypoxia.

摘要

光笼控技术有望实现对生物事件在时空上的精确操控。然而,目前的近红外(NIR)光笼在光解时依赖于氧气,且缺乏及时的反馈调节,这已被证明是靶向治疗的主要瓶颈。在此,我们提出了一种伴随发射片段产生的二烷基胺取代菁(Cy-NH)的缺氧依赖性光激活机制,该机制通过反合成和光谱分析得到了验证。我们首次在活细胞和荷瘤小鼠中实现了这种缺氧依赖性光笼的正交操控和双模态光学信号,在直接时空控制和体内反馈调节方面取得了突破。这种独特的光激活机制克服了缺氧的限制,允许对靶向治疗进行特定部位的远程控制,并扩展了光触发工具包,以按需释放药物,特别是在具有缺氧下双模态光学成像的生理环境中。

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