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

Zhou J. DengDepartment of Chemical Engineering, Massachusetts Institute of Technology, Rm 76-553, Cambridge, Massachusetts 02139, United StatesStephen W. MortonDepartment of Chemical Engineering, Massachusetts Institute of Technology, Rm 76-553, Cambridge, Massachusetts 02139, United StatesElana Ben‐AkivaDepartment of Chemical Engineering, Massachusetts Institute of Technology, Rm 76-553, Cambridge, Massachusetts 02139, United StatesErik C. DreadenDepartment of Chemical Engineering, Massachusetts Institute of Technology, Rm 76-553, Cambridge, Massachusetts 02139, United StatesKevin E. ShopsowitzDepartment of Chemical Engineering, Massachusetts Institute of Technology, Rm 76-553, Cambridge, Massachusetts 02139, United StatesPaula T. HammondDepartment of Chemical Engineering, Massachusetts Institute of Technology, Rm 76-553, Cambridge, Massachusetts 02139, United States
2013en
ABI

Аннотация

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.

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