Tumor-penetrating peptide modified and pH-sensitive polyplexes for tumor targeted siRNA delivery

被引:25
|
作者
Zhou, Guoyong [1 ]
Xu, Yongmin [1 ]
Chen, Meiwan [2 ]
Cheng, Du [1 ]
Shuai, Xintao [1 ,3 ]
机构
[1] Sun Yat Sen Univ, Sch Chem & Chem Engn, Minist Educ, PCFM Lab, Guangzhou 510275, Guangdong, Peoples R China
[2] Univ Macau, Inst Chinese Med Sci, State Key Lab Qual Res Chinese Med, Macau 999078, Peoples R China
[3] Sun Yat Sen Univ, Zhongshan Sch Med, BME Ctr, Guangzhou 510275, Guangdong, Peoples R China
基金
中国国家自然科学基金;
关键词
CANCER-THERAPY; IN-VIVO; POLYMERIC VECTOR; CELLULAR UPTAKE; CO-DELIVERY; NANOPARTICLES; DOXORUBICIN; REDUCTION; COPOLYMER; NANOCARRIER;
D O I
10.1039/c6py00427j
中图分类号
O63 [高分子化学(高聚物)];
学科分类号
070305 ; 080501 ; 081704 ;
摘要
A pH-sensitive ternary block copolymer comprising poly(ethylene glycol) methyl ether methacrylate (PEGMA), and pH-sensitive segments poly(2-(dimethylamino) ethylmethacrylate) (PDMA) and poly(2( diisopropyl amino) ethyl methacrylate) (PDPA) (mal-PEGMA-b-PDPA-b-PDMA, PMDM) was synthesized. The copolymer effectively complexed with siRNA at pH 5.0 to form a polyplex which showed decreased positive charge along with the increase of pH value due to deprotonation of the PDPA block. The nearly non-charged polyplex at pH 7.4 exhibited enhanced stability and inertness in serum-containing media, which is favorable for a prolonged circulation time and reduced cytotoxicity. The pH-sensitivity of PDMA and PDPA also enhanced the lysosomal escape of polyplexes after endocytosis. Moreover, modification of the tumor-penetrating peptide iRGD endowed the polyplexes with effective intratumoral delivery and high transfection efficiency. A study using the luciferase expression assay achieved highly effective target gene silencing both in vitro and in vivo, which revealed the potential of our iRGD-modified and pH-sensitive siRNA polyplex as a promising siRNA delivery system in cancer treatment.
引用
收藏
页码:3857 / 3863
页数:7
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