Layer-by-Layer Nanoparticles for Systemic Codelivery of an Anticancer Drug and siRNA for Potential Triple-Negative Breast Cancer Treatment

被引:456
作者
Deng, Zhou J. [1 ,2 ]
Morton, Stephen W. [1 ,2 ]
Ben-Akiva, Elana [1 ,2 ]
Dreaden, Erik C. [1 ,2 ]
Shopsowitz, Kevin E. [1 ,2 ]
Hammond, Paula T. [1 ,2 ]
机构
[1] MIT, Koch Inst Integrat Canc Res, Cambridge, MA 02139 USA
[2] MIT, Dept Chem Engn, Cambridge, MA 02139 USA
基金
加拿大自然科学与工程研究理事会;
关键词
layer-by-layer nanoparticles; siRNA delivery; doxorubicin; triple-negative breast cancer; combination therapy; SMALL INTERFERING RNA; GOLD NANOPARTICLES; INTRACELLULAR TRAFFICKING; DELIVERY; RECEPTOR; RESISTANCE; LIPOSOMES; MECHANISM; SURVIVAL; COMPLEX;
D O I
10.1021/nn4047925
中图分类号
O6 [化学];
学科分类号
070301 [无机化学];
摘要
A single nanoparticle platform has been developed through the modular and controlled layer-by-layer process to codeliver siRNA that knocks down a drug-resistance pathway in tumor cells and a chemotherapy drug to challenge a highly aggressive form of triple-negative breast cancer. Layer-by-layer films were formed on nanoparticles by alternately depositing siRNA and poly-L-arginine; a single bilayer on the nanoparticle surface could effectively load up to 3500 siRNA molecules, and the resulting LbL nanoparticles exhibit an extended serum half-life of 28 h. In animal models, one dose via intravenous administration significantly reduced the target gene expression in the tumors by almost 80%. By generating the siRNA-loaded film atop a doxorubicin-loaded liposome, we identified an effective combination therapy with siRNA targeting multidrug resistance protein 1, which significantly enhanced doxorubicin efficacy by 4 fold in vitro and led to up to an 8-fold decrease in tumor volume compared to the control treatments with no observed toxicity. The results indicate that the use of layer-by-layer films to modify a simple liposomal doxorubicin delivery construct with a synergistic siRNA can lead to significant tumor reduction in the cancers that are otherwise nonresponsive to treatment with Doxil or other common chemotherapy drugs. This approach provides a potential strategy to treat aggressive and resistant cancers, and a modular platform for a broad range of controlled multidrug therapies customizable to the cancer type in a singular nanoparticle delivery system.
引用
收藏
页码:9571 / 9584
页数:14
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