Dual-Responsive Mesoporous Silica Nanoparticles Mediated Codelivery of Doxorubicin and Bcl-2 SiRNA for Targeted Treatment of Breast Cancer

Dual-Responsive Mesoporous Silica Nanoparticles Mediated Codelivery of Doxorubicin and Bcl-2 SiRNA for Targeted Treatment of Breast Cancer
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双响应介孔二氧化硅纳米颗粒介导的多柔比星和 Bcl-2 SiRNA 共递送用于乳腺癌的靶向治疗

DOI:
10.1021/acs.jpcc.6b06759
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发表时间:
2016-09
影响因子:
3.7
通讯作者:
He, Chuanglong
He, Chuanglong
中科院分区:
化学3区
文献类型:
--
作者:
Qin, Ming;Mo, Xiumei;Wang, Hongsheng;He, Chuanglong

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化疗与基因治疗的联合应用可提高肿瘤的治疗效果。为了实现这一目标,开发了一种新的基于介孔二氧化硅纳米颗粒(MSNs)的共递送系统,用于靶向同时递送多柔比星(DOX)和Bcl-2小干扰RNA(siRNA)进入乳腺癌细胞。通过二硫键修饰聚乙烯亚胺-聚赖氨酸共聚物(PEI-PLL),并与叶酸连接的聚乙二醇(FA-PEG)偶联,制备了多功能MSNs(MSNs-PPPFA)。多功能MSNs-PPPFA纳米载体具有将DOX包封到MSNs的介孔通道中的能力,同时通过阳离子MSNs-PPPFA和阴离子siRNA之间的静电相互作用携带siRNA。所得的MSNs-PPPFA纳米颗粒用各种技术表征。药物释放结果表明,DOX从DOX-MSNs-PPPFA释放的pH和氧化还原都响应,和结果。
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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