纳米凝胶
纳米载体
光敏剂
脱镁叶绿酸A
化学
连接器
免疫原性细胞死亡
癌症研究
小干扰RNA
核酸
光动力疗法
程序性细胞死亡
核糖核酸
生物
生物化学
药物输送
细胞凋亡
操作系统
有机化学
基因
计算机科学
作者
Yuanyuan Guo,Qiushuang Zhang,Qiwen Zhu,Jing Gao,Xinyuan Zhu,Haijun Yu,Yuehua Li,Chuan Zhang
出处
期刊:Science Advances
[American Association for the Advancement of Science (AAAS)]
日期:2022-04-22
卷期号:8 (16)
被引量:63
标识
DOI:10.1126/sciadv.abn2941
摘要
Packaging multiple drugs into a nanocarrier with rational design to achieve synergistic cancer therapy remains a challenge due to the intrinsically varied pharmacodynamics of therapeutic agents. Especially difficult is combining small-molecule drugs and macromolecular biologics. Here, we successfully graft pheophorbide A (PPA) photosensitizers on DNA backbone at predesigned phosphorothioate modification sites. The synthesized four PPA-grafted DNAs are assembled into a tetrahedron framework, which further associates with a programmed death ligand-1 (PD-L1) small interfering RNA (siRNA) linker through supramolecular self-assembly to form an siRNA and PPA copackaged nanogel. With dual therapeutic agents inside, the nanogel can photodynamically kill tumor cells and induce remarkable immunogenic cell death. Also, it simultaneously silences the PD-L1 expression of the tumor cells, which substantially promotes the antitumor immune response and leads to an enhanced antitumor efficacy in a synergistic fashion.
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