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用于双光子激发光动力疗法和深部组织成像的可靶向溶酶体的聚噻吩纳米颗粒

Lysosome-targetable polythiophene nanoparticles for two-photon excitation photodynamic therapy and deep tissue imaging.

作者信息

Zhao Shaojing, Niu Guangle, Wu Feng, Yan Li, Zhang Hongyan, Zhao Junfang, Zeng Lintao, Lan Minhuan

机构信息

Tianjin Key Laboratory of Organic Solar Cells and Photochemical Conversion, School of Chemistry & Chemical Engineering, Tianjin University of Technology, Tianjin, China.

出版信息

J Mater Chem B. 2017 May 28;5(20):3651-3657. doi: 10.1039/c7tb00371d. Epub 2017 May 10.

Abstract

Two-photon excitation (TPE) photodynamic therapy (PDT) has attracted great interest due to its distinctive properties, e.g., good penetration ability of biological tissues and less damage to healthy tissues. However, the conventional photosensitizers (PSs) for PDT have poor subcellular location capability and low two-photon absorption (TPA) cross section in the phototherapeutic window. Herein, we report a fascinating multi-functional TPE PS, polythiophene nanoparticles (PT NPs), for simultaneous lysosome-targetable fluorescence imaging and PDT. PT NPs show bright yellow fluorescence, good water solubility as well as excellent photo- and pH-stability. Moreover, PT NPs exhibit high singlet oxygen generation quantum yield (∼42%) and large TPA cross section (∼3420 GM). A fluorescence imaging penetration depth of 1800 μm could be reached in the tissue phantom under the TPE mode. Due to these outstanding merits and their unique clathrin- and caveola-independent intracellular uptake pathway, PT NPs have great potential for application in TPE fluorescence imaging and photodynamic therapy.

摘要

双光子激发(TPE)光动力疗法(PDT)因其独特的性质,如生物组织穿透能力强和对健康组织损伤小等,而备受关注。然而,用于PDT的传统光敏剂(PSs)在光治疗窗口内的亚细胞定位能力差且双光子吸收(TPA)截面低。在此,我们报道了一种引人注目的多功能TPE PS,聚噻吩纳米颗粒(PT NPs),用于同时进行溶酶体靶向荧光成像和PDT。PT NPs呈现亮黄色荧光,具有良好的水溶性以及出色的光稳定性和pH稳定性。此外,PT NPs表现出高单线态氧生成量子产率(约42%)和大TPA截面(约3420 GM)。在TPE模式下,在组织模型中荧光成像穿透深度可达1800μm。由于这些突出优点及其独特的不依赖网格蛋白和小窝的细胞内摄取途径,PT NPs在TPE荧光成像和光动力疗法中具有巨大的应用潜力。

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