纳米颗粒
细胞凋亡
细胞毒性
癌细胞
药物输送
材料科学
转染
MTT法
基因沉默
活力测定
光热治疗
盐酸阿霉素
作者
Xiaojun Zhou,Liang Chen,Wei Nie,Weizhong Wang,Qin Ming,Xiumei Mo,Hongsheng Wang,Chuanglong He
标识
DOI:10.1021/acs.jpcc.6b06759
摘要
The combination of chemotherapy and gene therapy could induce the enhanced therapeutic efficacy in the cancer therapy. To achieve this goal, a new mesoporous silica nanoparticles (MSNs)-based codelivery system was developed for targeted simultaneous delivery of doxorubicin (DOX) and Bcl-2 small interfering RNA (siRNA) into breast cancer cells. The multifunctional MSNs (MSNs-PPPFA) were prepared by modification of polyethylenimine–polylysine copolymers (PEI-PLL) via the disulfide bonds, to which a targeting ligand folate-linked poly(ethylene glycol) (FA-PEG) was conjugated. The multifunctional MSNs-PPPFA nanocarrier has the ability to encapsulate DOX into the mesoporous channels of MSNs, while simultaneously carrying siRNA via electrostatic interaction between cationic MSNs-PPPFA and anionic siRNA. The resulting MSNs-PPPFA nanoparticles were characterized with various techniques. The drug release results reveal that DOX released from DOX-loaded MSNs-PPPFA are both pH- and redox-responsive, and the results ...
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