光动力疗法
材料科学
癌细胞
体内
生物物理学
细胞
细胞内
癌症研究
癌症
化学
生物化学
生物
遗传学
生物技术
有机化学
作者
Hong Bo Cheng,Jingyi Zhu,Shiying Li,Jin‐Yue Zeng,Qi Lei,Kewei Chen,Chi Zhang,Xian‐Zheng Zhang
标识
DOI:10.1002/adfm.201603212
摘要
Conventional oxygen‐dependent photodynamic therapy (PDT) has faced severe challenges because of the non‐specificity of most available photosensitizers (PSs) and the hypoxic nature of tumor tissues. Here, an O 2 self‐sufficient cell‐like biomimetic nanoplatform (CAT‐PS‐ZIF@Mem) consisting of the cancer cell membrane (Mem) and a cytoskeleton‐like porous zeolitic imidazolate framework (ZIF‐8) with the embedded catalase (CAT) protein molecules and Al(III) phthalocyanine chloride tetrasulfonic acid (AlPcS 4 , defined as PS) is developed. Because of the immunological response and homologous targeting abilities of the cancer cell membrane, CAT‐PS‐ZIF@Mem is selectively accumulated at the tumor site and taken up effectively by tumor cells after intravenous injection. After the intracellular H 2 O 2 penetration into the framework, it is catalyzed by CAT to produce O 2 at the hypoxic tumor site, facilitating the generation of toxic 1 O 2 for highly effective PDT in vivo under near‐infrared irradiation. By integrating the immune escape, cell homologous recognition, and O 2 self‐sufficiency, this cell‐like biomimetic nanoplatform demonstrates highly specific and efficient PDT against hypoxic tumor cells with much reduced side‐effect on normal tissues.
科研通智能强力驱动
Strongly Powered by AbleSci AI