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水溶性双(亚苄基)环烷酮类光敏剂敏化的异种移植瘤的有效双光子激发光动力疗法。

Effective Two-Photon Excited Photodynamic Therapy of Xenograft Tumors Sensitized by Water-Soluble Bis(arylidene)cycloalkanone Photosensitizers.

机构信息

Technical Institute of Physics and Chemistry, Chinese Academy of Sciences , 29 Zhongguancun East Road, Beijing 100190, P. R. China.

Institute of Process Engineering, National Key Laboratory of Biochemical Engineering, Chinese Academy of Sciences , Beijing 100190, P. R. China.

出版信息

J Med Chem. 2015 Oct 22;58(20):7949-58. doi: 10.1021/acs.jmedchem.5b00731. Epub 2015 Oct 1.

Abstract

A series of bis(arylidene)cycloalkanone photosensitizers modified by polyethylene glycol (PEG) have been studied for two-photon excited photodynamic therapy (2PE-PDT). As compared with their prototype compounds, these PEGylated photosensitizers show enhanced water solubilities while their photophysical and photochemical properties, including linear absorption, two-photon absorption, fluorescence, and singlet oxygen quantum yield, remain unaltered. In vitro behaviors (cellular uptake, subcellular localization, photocytotoxicity in both PDT and 2PE-PDT) of these photosensitizers reveal that an optimized lipid-water partition coefficient can be obtained by adjusting the length and position of the PEG chains. Among them, the photosensitizer modified asymmetrically by two tetraethylene glycol chains presents the best performance as a 2PE-PDT candidate. Selective blood-vessel closure and obvious therapeutic effect in inhibiting the growth of tumors are confirmed by in vivo 2PE-PDT after intravenous injection of this photosensitiezer. The survival periods of treated tumor-bearing mice are significantly prolonged. This study demonstrates the feasibility of using a simple molecule to construct a potential candidate for 2PE-PDT.

摘要

一系列通过聚乙二醇(PEG)修饰的双(亚苄基)环烷酮光引发剂已被研究用于双光子激发光动力疗法(2PE-PDT)。与原型化合物相比,这些聚乙二醇化的光引发剂具有更高的水溶性,同时其光物理和光化学性质,包括线性吸收、双光子吸收、荧光和单线态氧量子产率,保持不变。这些光引发剂的体外行为(细胞摄取、亚细胞定位、PDT 和 2PE-PDT 中的光细胞毒性)表明,可以通过调整 PEG 链的长度和位置来获得优化的油水分配系数。其中,通过两条四乙二醇链不对称修饰的光引发剂作为 2PE-PDT 的候选物表现出最佳性能。通过静脉注射该光引发剂后进行体内 2PE-PDT,证实了选择性血管闭合和抑制肿瘤生长的明显治疗效果。治疗的荷瘤小鼠的存活期明显延长。这项研究证明了使用简单分子构建潜在 2PE-PDT 候选物的可行性。

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