Clustering Small Dendrimers into Nanoaggregates for Efficient DNA and siRNA Delivery with Minimal Toxicity

被引:48
作者
Liu, Chongyi [1 ]
Shao, Naimin [1 ]
Wang, Yitong [1 ]
Cheng, Yiyun [1 ]
机构
[1] E China Normal Univ, Sch Life Sci, Shanghai Key Lab Regulatory Biol, Shanghai 200241, Peoples R China
基金
中国国家自然科学基金;
关键词
PHENYLBORONIC-ACID; GENE DELIVERY; AMPHIPHILIC DENDRIMER; POLYMERIC MICELLES; NANOPARTICLES; DESIGN; TUMORS; PROBE;
D O I
10.1002/adhm.201500679
中图分类号
R318 [生物医学工程];
学科分类号
0831 ;
摘要
Cationic dendrimers are widely used as nonviral gene vectors, however, current gene materials based on dendrimers are either little effective or too toxic on the transfected cells. Here, a facile strategy is presented to prepare high efficient dendrimers with low transfection toxicity. Small dendrimers with 2 nm are clustered into nanoaggregates (approximate to 100 nm) via phenylboronic acid modification and the self-assembled materials enable efficient DNA and siRNA delivery on several cell lines. The clustered nanostructures can disassemble into small dendrimers in acidic conditions thus exerting significantly less toxicity on the transfected cells. Further structure-function relationship studies reveal that both the phenyl group and boronic acid group play essential roles in the self-assembly and gene delivery processes. The transfection efficacy of phenylboronic acid-modified dendrimers can be down-regulated by blocking the boronic acid groups on dendrimers with diols or degrading the groups with hydrogen peroxide. This study provides a facile strategy in the development of efficient and biocompatible gene vectors based on low molecular weight polymers and clearly demonstrates the structure-function relationship of phenylboronic acid-modified polymers in gene delivery.
引用
收藏
页码:584 / 592
页数:9
相关论文
共 46 条
[1]   Dendrimers Designed for Functions: From Physical, Photophysical, and Supramolecular Properties to Applications in Sensing, Catalysis, Molecular Electronics, Photonics, and Nanomedicine [J].
Astruc, Didier ;
Boisselier, Elodie ;
Ornelas, Catia .
CHEMICAL REVIEWS, 2010, 110 (04) :1857-1959
[2]   Breaking up the correlation between efficacy and toxicity for nonviral gene delivery [J].
Breunig, Miriam ;
Lungwitz, Uta ;
Liebl, Renate ;
Goepferich, Achim .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2007, 104 (36) :14454-14459
[3]   Labile Catalytic Packaging of DNA/siRNA: Control of Gold Nanoparticles "out" of DNA/siRNA Complexes [J].
Chen, Alex M. ;
Taratula, Oleh ;
Wei, Dongguang ;
Yen, Hsin-I ;
Thomas, Thresia ;
Thomas, T. J. ;
Minko, Tamara ;
He, Huixin .
ACS NANO, 2010, 4 (07) :3679-3688
[4]   Phenylboronic-Acid-Modified Amphiphilic Polyether as a Neutral Gene Vector [J].
Chen, Fujie ;
Zhang, Zhenguo ;
Cai, Mengmeng ;
Zhang, Xiaojin ;
Zhong, Zhenlin ;
Zhuo, Renxi .
MACROMOLECULAR BIOSCIENCE, 2012, 12 (07) :962-969
[5]   Phenylboronic Acid-Installed Polymeric Micelles for Targeting Sialylated Epitopes in Solid Tumors [J].
Deshayes, Stephanie ;
Cabral, Horacio ;
Ishii, Takehiko ;
Miura, Yutaka ;
Kobayashi, Shutaro ;
Yamashita, Takashi ;
Matsumoto, Akira ;
Miyahara, Yuji ;
Nishiyama, Nobuhiro ;
Kataoka, Kazunori .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 2013, 135 (41) :15501-15507
[6]   Dendrimers in gene delivery [J].
Dufès, C ;
Uchegbu, IF ;
Schätzlein, AG .
ADVANCED DRUG DELIVERY REVIEWS, 2005, 57 (15) :2177-2202
[7]  
Gillet Jean-Pierre, 2009, V542, P5, DOI 10.1007/978-1-59745-561-9_1
[8]   Boronic acid-containing hydrogels: synthesis and their applications [J].
Guan, Ying ;
Zhang, Yongjun .
CHEMICAL SOCIETY REVIEWS, 2013, 42 (20) :8106-8121
[9]   Polymers modified with double-tailed fluorous compounds for efficient DNA and siRNA delivery [J].
He, Bingwei ;
Wang, Yitong ;
Shao, Naimin ;
Chang, Hong ;
Cheng, Yiyun .
ACTA BIOMATERIALIA, 2015, 22 :111-119
[10]   Dilution-Stable PAMAM G1-Grafted Polyrotaxane Supermolecules Deliver Gene into Cells through a Caveolae-Dependent Pathway [J].
Huang, Huan ;
Cao, Duanwen ;
Qin, Linghao ;
Tian, Shouqin ;
Liang, Yang ;
Pan, Shirong ;
Feng, Min .
MOLECULAR PHARMACEUTICS, 2014, 11 (07) :2323-2333