Targeted Gene Delivery to MCF-7 Cells Using Peptide-Conjugated Polyethylenimine

被引:17
|
作者
Mokhtarzadeh, Ahad [1 ,2 ]
Parhiz, Hamideh [1 ,2 ]
Hashemi, Maryam [3 ]
Ayatollahi, Sara [1 ,2 ]
Abnous, Khalil [1 ]
Ramezani, Mohammad [1 ,2 ]
机构
[1] Mashhad Univ Med Sci, Sch Pharm, Pharmaceut Res Ctr, Mashhad, Iran
[2] Mashhad Univ Med Sci, Sch Pharm, Dept Pharmaceut Biotechnol, Mashhad, Iran
[3] Mashhad Univ Med Sci, Sch Pharm, Nanotechnol Res Ctr, Mashhad, Iran
来源
AAPS PHARMSCITECH | 2015年 / 16卷 / 05期
关键词
breast cancer; gene therapy; phage-derived peptide; polyethylenimine; TRANSFECTION EFFICIENCY; PHAGE; DNA; EXPRESSION; VECTORS; THERAPY; DISPLAY; SIRNA;
D O I
10.1208/s12249-014-0208-6
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Specific and effective delivery of drugs and genes to cancer cells are the major issues in successful cancer treatment. Recently, targeted cancer gene therapy has been emerged as a main technology for the treatment of different types of cancers. Among various synthetic carriers, polyethylenimine is one of the most well-known polymers for gene delivery. In this study, we conjugated phage-derived peptide (DMPGTVLP) to polyethylenimine (10 kDa) via disulfide bonds for targeted gene delivery into breast adenocarcinoma cells (MCF-7). As negative-control cells, we used non-related hepatocellular carcinoma cells (HepG2). Peptide-conjugated polyplex exhibited low cytotoxicity and significantly increased the transfection efficiency in comparison with unmodified polyethylenimine. Therefore, the peptide-modified vector can be used as a good targeting agent for gene or drug delivery into breast adenocarcinoma cells.
引用
收藏
页码:1025 / 1032
页数:8
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