黑色素瘤
体内
癌症研究
体外
多西紫杉醇
脂质体
转移
小干扰RNA
癌基因
材料科学
肺
医学
癌症
化学
细胞培养
纳米技术
生物
转染
内科学
细胞周期
生物技术
生物化学
遗传学
作者
Yu Mi,Chaofeng Mu,Joy Wolfram,Zaian Deng,Ye Hu,Xuewu Liu,Elvin Blanco,Haifa Shen,Mauro Ferrari
标识
DOI:10.1002/adhm.201500910
摘要
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.
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