光动力疗法
材料科学
持续发光
生物发光成像
激发态
发光
体内
生物物理学
光电子学
化学
荧光素酶
生物
生物化学
热释光
基因
物理
生物技术
有机化学
核物理学
转染
作者
Tianhang Shi,Wenjing Sun,Ruixue Qin,Dong‐Sheng Li,Yushuo Feng,Lei Chen,Gang Liu,Xiaoyuan Chen,Hongmin Chen
标识
DOI:10.1002/adfm.202001166
摘要
Abstract Persistent luminescence imaging is accompanied by continuous illumination after the removal of excitation light, which can successfully prevent the generation of autofluorescence. In this study, a mesoporous silica template method is used to prepare uniform and monodisperse porous nanophosphors that can generate X‐ray‐excited persistent luminescence (XEPL). By loading photosensitizers, XEPL effectively excites the photosensitizers to produce reactive oxygen species for killing cancer cells. Imaging of orthotopic hepatic tumors in vivo shows that nanophosphors accumulate in the liver tumors through a passive targeting mechanism, as confirmed by the co‐imaging of bioluminescence and X‐ray‐excited luminescence. Under image‐guidance, X‐ray‐induced photodynamic therapy effectively inhibits the growth of orthotopic hepatic tumors with negligible side effects. Overall, X‐ray‐induced persistent luminescence promotes ultrasensitive imaging and effective inhibition of orthotopic hepatic tumors.
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