Cell-Targeting Cationic Gene Delivery System Based on a Modular Design Rationale

被引:28
作者
Liu, Jia [1 ]
Xu, Luming [1 ]
Jin, Yang [2 ]
Qi, Chao [1 ]
Li, Qilin [1 ]
Zhang, Yunti [3 ,4 ]
Jiang, Xulin [3 ,4 ]
Wang, Guobin [5 ]
Wang, Zheng [1 ,5 ]
Wang, Lin [1 ,6 ]
机构
[1] Huazhong Univ Sci & Technol, Tongji Med Coll, Union Hosp, Res Ctr Tissue Engn & Regenerat Med, Wuhan 430022, Peoples R China
[2] Huazhong Univ Sci & Technol, Tongji Med Coll, Union Hosp, Dept Respirat, Wuhan 430022, Hubei, Peoples R China
[3] Wuhan Univ, Minist Educ, Key Lab Biomed Polymers, Wuhan 430072, Peoples R China
[4] Wuhan Univ, Dept Chem, Wuhan 430072, Peoples R China
[5] Huazhong Univ Sci & Technol, Tongji Med Coll, Union Hosp, Dept Surg Gastroenterol, Wuhan 430022, Hubei, Peoples R China
[6] Huazhong Univ Sci & Technol, Tongji Med Coll, Union Hosp, Dept Clin Lab, Wuhan 430022, Hubei, Peoples R China
基金
中国国家自然科学基金;
关键词
gene delivery; disulfide bond; poly(ethylene glycol); cyclodextrin; folate; host-guest interaction; TRANSFER RADICAL POLYMERIZATION; NUCLEIC-ACID DELIVERY; MOLECULAR-WEIGHT; CO-DELIVERY; SIRNA; VECTORS; CANCER; DRUG; DNA; NANOPARTICLES;
D O I
10.1021/acsami.6b04462
中图分类号
TB3 [工程材料学];
学科分类号
0805 ; 080502 ;
摘要
En route to target cells, a gene carrier faces multiple extra- and intracellular hurdles that would affect delivery efficacy. Although diverse strategies have been proposed to functionalize gene carriers for individually overcoming these barriers, it is challenging to generate a single multifunctional gene carrier capable of surmounting all these barriers. Aiming at this challenge, we have developed a supramolecular modular approach to fabricate a multifunctional cationic gene delivery system. It consists of two prefunctionalized modules: (1) a host module: a polymer (PCD-SS-PDMAEMA) composed of poly(beta-cyclodextrin) backbone and disulfide-linked PDMAEMA arms, expectedly acting to compact DNA and release DNA upon cleavage of disulfide linkers in reductive microenvironment; and (2) a guest module: adamantyl and folate terminated PEG (Ad-PEG-FA), expectedly functioning to reduce nonspecific interactions, improve biocompatibility, and provide folate-mediated cellular targeting specificity. Through the host-guest interaction between beta-cyclodextrin units of the "host" module and adamantyl groups of the "guest" module, the PCD-SS-PDMAEMA-1 (host) and Ad-PEG-FA (guest) self-assemble forming a supramolecular pseudocopolymer (PCD-SS-PDMAEMA-1/PEG-FA). Our comprehensive analyses demonstrate that the functions preassigned to the two-building modules are well realized. The gene carrier effectively compacts DNA into stable nanosized polyplexes resistant to enzymatic digestion, triggers DNA release in reducing environment, possesses significantly improved hemocompatibility, and specifically targets folate-receptor positive cells. Most importantly, endowed with these predesigned functions, the PCD-SS-PDMAEMA-1/PEG-FA supramolecular gene carrier exhibits excellent transfection efficacy for both pDNA and siRNA. Thus, this work represents a-proof-of-concept example showing the efficiency and convenience of an adaptable, modular approach for conferring multiple functions to-a single supramolecular gene carrier toward effective in vivo delivery of therapeutic nucleic acids.
引用
收藏
页码:14200 / 14210
页数:11
相关论文
共 70 条
  • [1] Physicochemical and biological characterization of targeted, nucleic acid-containing nanoparticles
    Bartlett, Derek W.
    Davis, Mark E.
    [J]. BIOCONJUGATE CHEMISTRY, 2007, 18 (02) : 456 - 468
  • [2] Temperature-controlled properties of DNA complexes with poly(ethylenimine)-graft-poly(N-isopropylacrylamide)
    Bisht, HS
    Manickam, DS
    You, YZ
    Oupicky, D
    [J]. BIOMACROMOLECULES, 2006, 7 (04) : 1169 - 1178
  • [3] Supramolecular Coordination: Self-Assembly of Finite Two- and Three-Dimensional Ensembles
    Chakrabarty, Rajesh
    Mukherjee, Partha Sarathi
    Stang, Peter J.
    [J]. CHEMICAL REVIEWS, 2011, 111 (11) : 6810 - 6918
  • [4] Cyclodextrin-based inclusion complexation bridging supramolecular chemistry and macromolecular self-assembly
    Chen, Guosong
    Jiang, Ming
    [J]. CHEMICAL SOCIETY REVIEWS, 2011, 40 (05) : 2254 - 2266
  • [5] A surface charge-switchable and folate modified system for co-delivery of proapoptosis peptide and p53 plasmid in cancer therapy
    Chen, Si
    Rong, Lei
    Lei, Qi
    Cao, Peng-Xi
    Qin, Si-Yong
    Zheng, Di-Wei
    Jia, Hui-Zhen
    Zhu, Jing-Yi
    Cheng, Si-Xue
    Zhuo, Ren-Xi
    Zhang, Xian-Zheng
    [J]. BIOMATERIALS, 2016, 77 : 149 - 163
  • [6] Enzymatic PEGylated Poly(lactone-co-β-amino ester) Nanoparticles as Biodegradable, Biocompatible and Stable Vectors for Gene Delivery
    Chen, Ya
    Li, Yingqin
    Gao, Jinbiao
    Cao, Zhong
    Jiang, Qing
    Liu, Jie
    Jiang, Zhaozhong
    [J]. ACS APPLIED MATERIALS & INTERFACES, 2016, 8 (01) : 490 - 501
  • [7] Progresses towards safe and efficient gene therapy vectors
    Chira, Sergiu
    Jackson, Carlo S.
    Oprea, Iulian
    Ozturk, Ferhat
    Pepper, Michael S.
    Diaconu, Iulia
    Braicu, Cornelia
    Raduly, Lajos-Zsolt
    Calin, George A.
    Berindan-Neagoe, Ioana
    [J]. ONCOTARGET, 2015, 6 (31) : 30675 - 30703
  • [8] Agmatine-Containing Bioreducible Polymer for Gene Delivery Systems and Its Dual Degradation Behavior
    Choi, Ji-yeong
    Ryu, Kitae
    Lee, Gyeong Jin
    Kim, Kyunghwan
    Kim, Tae-il
    [J]. BIOMACROMOLECULES, 2015, 16 (09) : 2715 - 2725
  • [9] Advances in fabricating double-emulsion droplets and their biomedical applications
    Chong, DaoTong
    Liu, XinShi
    Ma, HuaJie
    Huang, GuoYou
    Han, Yu Long
    Cui, XingYe
    Yan, JunJie
    Xu, Feng
    [J]. MICROFLUIDICS AND NANOFLUIDICS, 2015, 19 (05) : 1071 - 1090
  • [10] Delivery of DNA and siRNA by novel gemini-like amphiphilic peptides
    Damen, Mark
    Aarbiou, Jamil
    van Dongen, Stijn F. M.
    Buijs-Offerman, Ruvalic M.
    Spijkers, Patricia P.
    van den Heuvel, Maaike
    Kvashnina, Kristina
    Nolte, Roeland J. M.
    Scholte, Bob J.
    Feiters, Martin C.
    [J]. JOURNAL OF CONTROLLED RELEASE, 2010, 145 (01) : 33 - 39