Co-delivery of siRNA and therapeutic agents using nanocarriers to overcome cancer resistance

被引:290
作者
Creixell, Mar [1 ]
Peppas, Nicholas A. [1 ,2 ,3 ]
机构
[1] Univ Texas Austin, Dept Chem Engn, Austin, TX 78712 USA
[2] Univ Texas Austin, Dept Biomed Engn, Austin, TX 78712 USA
[3] Univ Texas Austin, Coll Pharm, Austin, TX 78712 USA
基金
美国国家科学基金会; 美国国家卫生研究院;
关键词
Co-delivery; siRNA; Cancer therapy; Multi drug resistance; (MDR); Nanoparticles; Doxorubicin; SMALL-INTERFERING RNA; MESOPOROUS SILICA NANOPARTICLES; MULTIDRUG-RESISTANCE; P-GLYCOPROTEIN; DRUG-DELIVERY; LIPID NANOPARTICLES; ANTICANCER DRUG; POLYMER NANOPARTICLES; EFFICIENT DELIVERY; TUMOR-GROWTH;
D O I
10.1016/j.nantod.2012.06.013
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
There are two main mechanisms by which cells become multidrug resistant (MDR): by increasing drug efflux pumps on the cell membrane and by increasing anti-apoptotic pathways. The use of nanotechnology to develop nanodelivery systems has allowed researchers to overcome limitations of antineoplastic drugs by increasing the solubility of the drug and decreasing the toxicity to healthy tissues. By encapsulating drugs into nanoparticles that bypass the efflux pumps, drug efflux is reduced, hence increasing the intracellular concentration of the drug. siRNA has the ability to disrupt cellular pathways by knocking down genes, opening the door to down regulating anti-apoptotic pathways. The use of nanocarriers to deliver siRNA, prevents both renal clearance and RNase degradation by protecting siRNA chains, increasing their half life in blood. It has been suggested that codelivering drugs and siRNA together in the same delivery system would be more effective in overcoming resistance of cancer cells than co-treatment of cancer cells with delivery systems carrying either siRNA or drugs. In this study we discuss the progress of nanoscale co-delivery systems in overcoming multidrug cancer resistance. (c) 2012 Elsevier Ltd. All rights reserved.
引用
收藏
页码:367 / 379
页数:13
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