光动力疗法
光毒性
化学
光敏剂
前药
癌症研究
细胞毒性
肿瘤细胞
肿瘤微环境
放射治疗
肝细胞癌
药物输送
胶束
羧酸酯酶
生物安全
毒品携带者
吲哚青绿
恶性细胞
免疫疗法
转移
药理学
作者
Huihui Liu,Jie Guo,Wu Yin,Hehua Xiong,Ling Chen,Yiling Ruan,Kai Feng,Dan Su,Yi Liu,Xiaolian Sun
标识
DOI:10.1021/acs.jmedchem.5c02387
摘要
Zr-PHZ-BrCyE exhibited robust tumor inhibition and excellent biosafety in both subcutaneous and orthotopic H22 tumor models. This approach holds great promise for improving the therapeutic outcomes of CR-PDT in deep-seated tumors while ensuring good biosafety, paving the way for future potential clinical applications in the future.
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