| Literature DB >> 26890862 |
Yu Mi1, Chaofeng Mu1, Joy Wolfram1, Zaian Deng1, Tony Ye Hu1, Xuewu Liu1, Elvin Blanco1, Haifa Shen1,2, Mauro Ferrari1,3.
Abstract
The successful treatment of malignant disease generally requires the use of multiple therapeutic agents that are coordinated in a spatiotemporal manner to enable synergy. Here, a porous silicon-based micro/nano composite (MNC) that is capable of simultaneously delivering chemotherapeutic agents and small interfering RNA (siRNA) to the lungs following intravenous injection is designed. The pores of the silicon microparticles are loaded with B-Raf proto-oncogene serine/threonine kinase (BRAF) siRNA-containing liposomes, while the surface is conjugated with docetaxel-encapsulated polymeric nanoparticles. The synergistic antitumor effect of the MNC is demonstrated in vitro in melanoma cells and in vivo using a mouse model for melanoma lung metastasis. The MNC displays superior therapeutic efficacy and increased accumulation in metastatic melanoma lesions in the lungs in comparison to combination therapy with liposomes and polymers. The results indicate that the MNC can be used as an effective delivery vehicle for simultaneous enrichment of multiple therapeutic agents in the lungs.Entities:
Keywords: biomaterials; drug delivery; melanoma lung metastasis; polymeric materials; siRNA delivery; silicon microdisks
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Year: 2016 PMID: 26890862 PMCID: PMC4837059 DOI: 10.1002/adhm.201500910
Source DB: PubMed Journal: Adv Healthc Mater ISSN: 2192-2640 Impact factor: 9.933