| Literature DB >> 25856302 |
Lei Wang1, Yongwei Hao1, Haixia Li1, Yalin Zhao1, Dehui Meng1, Dong Li1, Jinjin Shi1, Hongling Zhang1, Zhenzhong Zhang1, Yun Zhang1.
Abstract
It is very challenging to treat brain cancer because of the blood-brain barrier (BBB) restricting therapeutic drug or gene to access the brain. In this research project, angiopep-2 (ANG) was used as a brain-targeted peptide for preparing multifunctional ANG-modified poly(lactic-co-glycolic acid) (PLGA) nanoparticles (NPs), which encapsulated both doxorubicin (DOX) and epidermal growth factor receptor (EGFR) siRNA, designated as ANG/PLGA/DOX/siRNA. This system could efficiently deliver DOX and siRNA into U87MG cells leading to significant cell inhibition, apoptosis and EGFR silencing in vitro. It demonstrated that this drug system was capable of penetrating the BBB in vivo, resulting in more drugs accumulation in the brain. The animal study using the brain orthotopic U87MG glioma xenograft model indicated that the ANG-targeted co-delivery of DOX and EGFR siRNA resulted in not only the prolongation of the life span of the glioma-bearing mice but also an obvious cell apoptosis in glioma tissue.Entities:
Keywords: Blood–brain barrier; DOX; brain delivery; drug delivery; siRNA
Mesh:
Substances:
Year: 2015 PMID: 25856302 DOI: 10.3109/1061186X.2015.1025077
Source DB: PubMed Journal: J Drug Target ISSN: 1026-7158 Impact factor: 5.121