中国科学院机构知识库网格
Chinese Academy of Sciences Institutional Repositories Grid
Carboxymethyl dextran-stabilized polyethylenimine-poly(epsilon-caprolactone) nanoparticles-mediated modulation of microrna-34a expression via small-molecule modulator for hepatocellular carcinoma therapy

文献类型:期刊论文

作者Deng, Xiongwei1,2; Yin, Zhaoxia1; Zhou, Zhixiang1; Wang, Yihui1; Zhang, Fang1; Hu, Qin1; Yang, Yishu1; Lu, Jianqing2; Wu, Yan2; Sheng, Wang1
刊名Acs applied materials & interfaces
出版日期2016-07-13
卷号8期号:27页码:17068-17079
关键词Carboxymethyl dextran Polyethylenimine-poly(epsilon-caprolactone) Nanoparticles Microrna modulation Small-molecule modulator Hepatocellular carcinoma
ISSN号1944-8244
DOI10.1021/acsami.6b03122
通讯作者Wu, yan(wuy@nanoctr.cn) ; Sheng, wang(shengwang@bjut.edu.cn)
英文摘要Microrna-34a (mir-34a) modulation therapy has shown great promise to treat hepatocellular carcinoma (hcc). 2'-hydroxy-2,4,4',5,6'-pentamethoxychalcone, termed rubone, has been shown to specifically upregulate mir-34a expression in hcc cells and considered as novel anticancer agent. however, the extremely low aqueous solubility of rubone hampers its use in cancer treatment. in the present study, surface-stabilized nanoparticles-based delivery strategy was engaged to overcome this impediment. in our preparation, rubone was encapsulated in the micelles composed of polyethylenimine-poly(epsilon-caprolactone) (pei-pcl) through hydrophobic interactions, which were subsequently stabilized with anionic carboxymethyl dextran cmd via electronic interaction. we found that rubone-encapsulating nanoparticles are dispersed well in aqueous solution. the results further demonstrated that rubone could be efficiently delivered in hcc cells by nanoparticles and upregulate mir-34a expression, which in turn led to inhibition of proliferation, migration, and increased apoptosis of hcc cells. in vivo experiments showed that rubone can be preferentially delivered into tumor tissues by cmd-stabilized pei-pcl nanoparticles after intravenous administration and significantly inhibited tumor growth. furthermore, low cytotoxicity of the nanoparticles was observed in vitro and in vivo analyses, indicating a good compatibility of generated nanoparticles. the obtained results suggest that cmd-stabilized pei-pcl nanoparticles may serve as a novel approach for small-molecule-modulator mediated mir-34a restoration for hcc therapy.
WOS关键词NEGATIVE BREAST-CANCER ; DRUG-DELIVERY ; POLYMERIC NANOPARTICLES ; INTRACELLULAR DELIVERY ; IN-VIVO ; ACID ; PH ; NANOMATERIALS ; BINDING ; DESIGN
WOS研究方向Science & Technology - Other Topics ; Materials Science
WOS类目Nanoscience & Nanotechnology ; Materials Science, Multidisciplinary
语种英语
WOS记录号WOS:000379794100009
出版者AMER CHEMICAL SOC
URI标识http://www.irgrid.ac.cn/handle/1471x/2176598
专题高能物理研究所
通讯作者Wu, Yan; Sheng, Wang
作者单位1.Beijing Univ Technol, Coll Life Sci & Bioengn, 100 Pingleyuan, Beijing 100124, Peoples R China
2.Natl Ctr Nanosci & Technol, CAS Ctr Excellence Nanosci, CAS Key Lab Biomed Effects Nanomat & Nanosafety, 11 Beiyitiao, Beijing 100190, Peoples R China
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GB/T 7714
Deng, Xiongwei,Yin, Zhaoxia,Zhou, Zhixiang,et al. Carboxymethyl dextran-stabilized polyethylenimine-poly(epsilon-caprolactone) nanoparticles-mediated modulation of microrna-34a expression via small-molecule modulator for hepatocellular carcinoma therapy[J]. Acs applied materials & interfaces,2016,8(27):17068-17079.
APA Deng, Xiongwei.,Yin, Zhaoxia.,Zhou, Zhixiang.,Wang, Yihui.,Zhang, Fang.,...&Zeng, Yi.(2016).Carboxymethyl dextran-stabilized polyethylenimine-poly(epsilon-caprolactone) nanoparticles-mediated modulation of microrna-34a expression via small-molecule modulator for hepatocellular carcinoma therapy.Acs applied materials & interfaces,8(27),17068-17079.
MLA Deng, Xiongwei,et al."Carboxymethyl dextran-stabilized polyethylenimine-poly(epsilon-caprolactone) nanoparticles-mediated modulation of microrna-34a expression via small-molecule modulator for hepatocellular carcinoma therapy".Acs applied materials & interfaces 8.27(2016):17068-17079.

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