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基于金属的光激活化疗(PACT)化合物的细胞毒性。

Cytotoxicity of Metal-Based Photoactivated Chemotherapy (PACT) Compounds.

机构信息

Leiden Institute of Chemistry, Leiden University, Leiden, The Netherlands.

出版信息

Methods Mol Biol. 2022;2451:245-258. doi: 10.1007/978-1-0716-2099-1_17.

Abstract

Metal-based compounds have been used to treat cancer for decades, with cisplatin being the most common and widely used. Photodynamic therapy (PDT) is another clinical modality used to fight cancer, which uses a photosensitizer (PS) that localizes in cancer tissues. This PS is activated by the illumination of the tumor with visible light. Photoactivated chemotherapy (PACT) is a new concept that brings these two ideas together. Like PDT , PACT aims at sparing healthy tissues while maintaining toxicity against cancerous cells. Unlike PDT , which often stops working when the concentration of dioxygen in illuminated tissues is too low, light activation of PACT compounds remains efficient in hypoxic cancer cells. This chapter addresses the methodology to experimentally measure the phototoxicity of PACT compounds in cancer cell lines, under both normoxic and hypoxic conditions.

摘要

金属基化合物已被用于治疗癌症数十年,顺铂是最常见和广泛使用的一种。光动力疗法(PDT)是另一种用于治疗癌症的临床方法,它使用一种定位于癌症组织中的光敏剂(PS)。这种 PS 通过可见光照射肿瘤而被激活。光激活化疗(PACT)是一个新概念,它将这两种理念结合在一起。与 PDT 一样,PACT 的目的是在保留对癌细胞毒性的同时,避免健康组织受到伤害。与 PDT 不同,当被照射组织中的二氧化氮浓度过低时,PDT 往往会失效,而 PACT 化合物的光激活在缺氧的癌细胞中仍然有效。本章介绍了在常氧和缺氧条件下,在癌细胞系中实验测量 PACT 化合物光毒性的方法。

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