CAS Key Laboratory of Nanosystem and Hierarchical Fabrication, CAS Center for Excellence in Nanoscience, National Center for Nanoscience and Technology, No. 11 BeiYiTiao, ZhongGuanCun, Beijing 100190, China.
Nanoscale. 2017 Jun 14;9(23):7750-7754. doi: 10.1039/c7nr02222k.
We herein demonstrate that DNA origami can work as a multifunctional platform integrating a chemotherapeutic drug (doxorubicin), gold nanorods and a tumour-specific aptamer MUC-1, to realize the effective circumvention of drug resistance. Doxorubicin (DOX) was loaded efficiently onto DNA origami through base pair intercalation and surface-modified gold nanorods (AuNRs) were assembled onto the DNA origami through DNA hybridization. Due to the active targeting effect of the assembled aptamers, the multifunctional nanostructures achieved increased cellular internalization of DOX and AuNRs. Upon near-infrared (NIR) laser irradiation, the P-glycoprotein (multidrug resistance pump) expression of multidrug resistant MCF-7 (MCF-7/ADR) cells was down-regulated, achieving the synergistically chemotherapeutic (DOX) and photothermal (AuNRs) effects.
我们在此证明 DNA 折纸术可以作为一个多功能平台,整合化疗药物(阿霉素)、金纳米棒和肿瘤特异性适体 MUC-1,以实现有效的耐药性规避。阿霉素(DOX)通过碱基对嵌入高效加载到 DNA 折纸术上,表面修饰的金纳米棒(AuNRs)通过 DNA 杂交组装到 DNA 折纸术上。由于组装适体的主动靶向作用,多功能纳米结构实现了 DOX 和 AuNRs 的细胞内化增加。近红外(NIR)激光照射下,多药耐药 MCF-7(MCF-7/ADR)细胞的 P-糖蛋白(多药耐药泵)表达下调,协同化疗(DOX)和光热(AuNRs)效应。