光动力疗法
光毒性
钌
双光子激发显微术
化学
赫拉
光化学
溶酶体
选择性
组合化学
生物物理学
纳米技术
材料科学
荧光
生物化学
生物
有机化学
光学
催化作用
体外
酶
物理
作者
Huaiyi Huang,Bole Yu,Pingyu Zhang,Juanjuan Huang,Yu Chen,Gilles Gasser,Liang‐Nian Ji,Hui Chao
标识
DOI:10.1002/anie.201507800
摘要
Abstract Photodynamic therapy (PDT) is a noninvasive medical technique that has received increasing attention over the last years and been applied for the treatment of certain types of cancer. However, the currently clinically used PDT agents have several limitations, such as low water solubility, poor photostability, and limited selectivity towards cancer cells, aside from having very low two‐photon cross‐sections around 800 nm, which limits their potential use in TP‐PDT. To tackle these drawbacks, three highly positively charged ruthenium(II) polypyridyl complexes were synthesized. These complexes selectively localize in the lysosomes, an ideal localization for PDT purposes. One of these complexes showed an impressive phototoxicity index upon irradiation at 800 nm in 3D HeLa multicellular tumor spheroids and thus holds great promise for applications in two‐photon photodynamic therapy.
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