光热治疗
胶质母细胞瘤
血脑屏障
材料科学
光动力疗法
脑瘤
胶质瘤
分子成像
分子探针
生物医学工程
医学
癌症研究
体内
生物物理学
磁共振成像
纳米技术
病理
生物
内科学
放射科
中枢神经系统
生物化学
化学
DNA
有机化学
生物技术
作者
Bo Li,Hong Xiao,Mingyue Cai,Mingqiang Li,Xiaolin Xu,Shiyin Wang,Si Huang,Yong Wang,Du Cheng,Pengfei Pang,Hong Shan,Xintao Shuai
标识
DOI:10.1002/adfm.201909117
摘要
Abstract Currently, treatment of intracranial diseases still remains a great challenge because the blood–brain barrier (BBB) blocks access of most drugs to the central nervous system. Herein, a theranostic small molecular probe, iRGD‐ICG‐Lys‐DTPA@Gd (iRGD‐ILD), capable of crossing BBB is developed. Owing to the small molecular size and α v β 3 integrin receptor–mediated transcytosis, this tailor‐made molecular probe integrating the fluorescence and magnetic resonance imaging functions effectively passes through BBB to target tumor cells even in the early stage of glioblastoma multiforme (GBM), thereby allowing a bimodal imaging–guided therapy of GBM. The reactive oxygen species and heat generated by the ICG moiety under the 808 nm laser irradiation exert photodynamic/photothermal therapeutic effects, which results in significantly inhibited tumor growth and prolonged median survival of C6‐Luc glioma‐bearing mice. Notably, the integration of FDA‐approved clinically available agents, e.g., ICG, DTPA and Gd, into a molecular probe may ensure desirable biocompatibility and biosafety for in vivo applications. Overall, the results highlight the potential of a water‐soluble small molecule as a novel theranostic probe for highly effective GBM treatment.
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