| Literature DB >> 26444082 |
Xiaoying Zhuang1, Yun Teng1, Abhilash Samykutty1, Jingyao Mu1, Zhongbin Deng1, Lifeng Zhang1, Pengxiao Cao1, Yuan Rong1, Jun Yan1, Donald Miller1, Huang-Ge Zhang1,2.
Abstract
The lack of access to the brain is a major obstacle for central nervous system drug development. In this study, we demonstrate the capability of a grapefruit-derived nanovector (GNV) to carry miR17 for therapeutic treatment of mouse brain tumor. We show that GNVs coated with folic acid (FA-GNVs) are enhanced for targeting the GNVs to a folate receptor-positive GL-26 brain tumor. Additionally, FA-GNV-coated polyethylenimine (FA-pGNVs) not only enhance the capacity to carry RNA, but the toxicity of the polyethylenimine is eliminated by the GNVs. Intranasal administration of miR17 carried by FA-pGNVs led to rapid delivery of miR17 to the brain that was selectively taken up by GL-26 tumor cells. Mice treated intranasally with FA-pGNV/miR17 had delayed brain tumor growth. Our results demonstrate that this strategy may provide a noninvasive therapeutic approach for treating brain-related disease through intranasal delivery.Entities:
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Year: 2015 PMID: 26444082 PMCID: PMC4754550 DOI: 10.1038/mt.2015.188
Source DB: PubMed Journal: Mol Ther ISSN: 1525-0016 Impact factor: 11.454