期刊文献+

新型纳米材料HPC-g-PDMAEMA作为基因载体的研究

Evaluation of the Novel Nanoparticles HPC-g-PDMAEMA as Gene Delivery System
原文传递
导出
摘要 目的研究新型纳米载体HPC-g-PDMAEMA(HPD)对于不同肿瘤细胞系的转染能力,评价其在基因治疗及研究中的作用,并且初步探索HPD对于siRNA的运载能力。方法 HPD和脂质体2000(Lipo 2K)运载绿色荧光蛋白(GFP)质粒,分别转染MCF7、973、JF305 3种肿瘤细胞系,采用流式细胞仪检测其转染效率;HPD和Lipo 2K运载针对GADPH的siRNA,转染MCF7,利用RT-PCR检测其RNA转染效率。结果对于MCF7细胞,HPD的DNA转染效率高于Lipo 2K;对于973细胞,二者转染效率相近;对于JF305细胞,HPD转染效率低于Lipo 2K。在MCF7细胞中,利用HPD进行RNA转染,效率低于Lipo 2K。结论对于不同的肿瘤细胞系,可以采用不同的基因载体进行转染,从而提高转染效率。 OBJECTIVE To study the DNA transfection efficiencies of the novel cationic polymers HPC-g-PDMAEMA(HPD) for tumor cells.To evaluate the capacity of HPD as siRNA carrier for gene therapy.METHOD DNA transfection assays were performed using HPD/pEGFP-C1 complexes in MCF7,973,JF305 cells and the cellular uptake was determined by flow cytometry.RNA transfection assays were performed using HPD/GADPH siRNA complexes in MCF7 cell and mRNA expression was analyzed by RT-PCR.RESULTS The gene transfection efficiency of HPD/pEGFP-C1 complexes is higher in MCF7,similar in 973 and lower in JF305 than those of Lipo 2K,however,the transfection efficiency of HPD/RNA complexes is lower than that of Lipo 2K.CONCLUSION Gene delivery systems can be used distinctively in different tumor cell lines for efficient tumor-specific gene therapy.
出处 《中国药学杂志》 CAS CSCD 北大核心 2010年第14期1080-1084,共5页 Chinese Pharmaceutical Journal
关键词 HPC-g-PDMAEMA 脂质体2000 绿色荧光蛋白质粒 GADPH SIRNA HPC-g-PDMAEMA lipofectamine 2000 pEGFP-C1 GADPH siRNA
  • 相关文献

参考文献15

  • 1WAGNER E, KLOECKER J. Gene delivery using polymer therapeutics [ J ]. Adv Polym Sci, 2006,192 ( 2 ) : 135-173.
  • 2MINTZER M A, SIMANEK E E. Nonviral vectors for gene delivery[J]. Chem Rev, 2009,109(2) :259-302.
  • 3SCHWENDENER R A. Liposomes in biology and medicine[ J ]. Adv Exp Med Biol, 2007, 620(2) :117-128.
  • 4FELGNER P L, TSAI Y J, SUKHU L, et al. Improved cationic lipid formulations for in vivo genc therapy [ J ]. Ann NY Acad Sci, 1995, 27,772(2) :126-139.
  • 5ELIYAHU H, BARENHOLZ Y, DOMB A J. Polymers for DNA delivery [ J]. Molecules, 2005,10( 1 ) :34-64.
  • 6DE SMEDT S C, DEMEESTERM J, HENNINK W E. Cationic polymer based gene delivery systems [ J ]. Pharm Res, 2000,17 (2) :113-126.
  • 7YANG C, LI H, GOH S H, et al. Cationic star polymers consisting of R-cyclodextrin core and oligoethylenimine arms as nonviral gene delivery vectors [ J ]. Biomaterials, 2007,28 ( 21 ) : 3245- 3254.
  • 8OSTMARK E, HARRISSON S, WOOLEY K L, et al. Comb polymers prepared by ATRP from hydroxypropyl cellulose [ J ]. Biomacromolecules, 2007,8 (4) : 1138- 1148.
  • 9MARSANO E, BLANCHI E, SCIUTFO L. Microporous thermally sensitive hydrogels based on hydroxypropyl cellulose crosslinked with poly-ethyleneglicol diglycidyl ether[ J]. Polymer, 2003,44(22) :6835-6841.
  • 10XU F J, PING Y, MA J, et al. Comb-shaped copolymers composed of hydroxyproyl cellulose backbones and cationic poly( (2- dimethyl amino)ethyl methacrylate) side chains for gene delivery [ J ]. Bioconjugate Chem, 2009,20 ( 8 ) : 1449-1458.

相关作者

内容加载中请稍等...

相关机构

内容加载中请稍等...

相关主题

内容加载中请稍等...

浏览历史

内容加载中请稍等...
;
使用帮助 返回顶部