Lipid Nanoparticles Composed of Quaternary Amine-Tertiary Amine Cationic Lipid Combination (QTsome) for Therapeutic Delivery of AntimiR-21 for Lung Cancer

被引:59
作者
Yung, Bryant C. [1 ]
Li, Jilong [1 ]
Zhang, Mengzi [2 ]
Cheng, Xinwei [3 ]
Li, Hong [1 ]
Yung, Elaine M. [1 ]
Kang, Chen [4 ]
Cosby, Lauren E. [3 ]
Liu, Yang [1 ]
Teng, Lesheng [5 ]
Lee, Robert J. [1 ,2 ,3 ,5 ]
机构
[1] Ohio State Univ, Coll Pharm, Div Pharmaceut, 500 W 12th Ave, Columbus, OH 43210 USA
[2] Ohio State Univ, Mol Cellular & Dev Biol Program, Columbus, OH 43210 USA
[3] Ohio State Univ, Coll Engn, Dept Biomed Engn, Columbus, OH 43210 USA
[4] Ohio State Univ, Coll Pharm, Div Pharmacol, Columbus, OH 43210 USA
[5] Jilin Univ, Coll Life Sci, Changchun 130023, Peoples R China
关键词
nanoparticles; microRNA; cancer; drug delivery; RNA interference; noncoding RNA; gene regulation; PROGNOSTIC VALUE; DRUG-RESISTANCE; EXPRESSION; MIR-21; STABILITY; PCR;
D O I
10.1021/acs.molpharmaceut.5b00878
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
microRNA-21 (miR-21) is an oncomiR that is frequently upregulated in human cancers. AntimiR-21 (AM-21) is an oligonucleotide complementary to miR-21 that is designed to inhibit its gene silencing activities. To facilitate efficient delivery of AM-21, a novel lipid nanoparticle formulation called QTsome, based on a combination of quaternary amine and tertiary amine cationic lipids, with a distinctive pH-responsive profile, was developed. QTsome/AM-21 comprising DODMA/DOTAP/DOPC/CHOL/mPEG-DPPE and AM-21 oligonucleotide exhibited a mean particle diameter of below 150 nm, moderate zeta potential (+13.2 excellent colloidal stability, and high drug loading efficiency (above 80%). In vitro study showed QTsome/AM21 induced upregulation of miR-21 targets, including PTEN and DDAH1, in A549 cells while increasing their sensitivity toward paclitaxel (PTX). Finally, tumor regression, prolonged survival, and miR-21 target upregulation were demonstrated in an A549 xenograft mouse model. These data suggest that QTsome/AM-21 warrants further evaluation as an anticancer agent.
引用
收藏
页码:653 / 662
页数:10
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