siRNA-functionalized lanthanide nanoparticle enables efficient endosomal escape and cancer treatment
Chanchan Yu, Kun Li, Lin Xu, Bo Li, Chunhui Li, Shuai Guo, Ziyue Li, Yuquan Zhang, Abid Hussain, Hong Tan, Mengyu Zhang, Yongxiang Zhao, Yuanyu Huang, Xing‐Jie Liang
Abstract
Attaching DNA/RNA to nanomaterials is the basis for nucleic acid-based assembly and drug delivery. Herein, we report that small interfering RNA (siRNA) effectively coordinates with ligand-free lanthanide nanoparticles (NaGdF 4 NPs), and forms siRNA/NaGdF 4 spherical nucleic acids (SNA). The coordination is primarily attributed to the interaction between Gd and phosphate backbone of the siRNA. Surprisingly, an efficient encapsulation and rapid endosomal escape of siRNA from the endosome/lysosome were achieved, due to its flexible ability to bound to phospholipid head of endosomal membrane, thereby disrupting the membrane structure. Resorting to the dual properties of NaGdF 4 NPs, siRNA loading, and endosomal escape, siRNA targeting programmed cell death-ligand 1 (siPD-L1)/NaGdF 4 SNA triggers significant gene silencing in vitro and in vivo , and effectively represses the tumor growth in both CT26 tumor model and 4T1 orthotopic murine model.