Modular Construction of Multifunctional Bioresponsive Cell-Targeted Nanoparticles for Gene Delivery

被引:43
|
作者
Saeed, Aram O.
Magnusson, Johannes P.
Moradi, Emilia
Soliman, Mahmoud [4 ]
Wang, Wenxin [3 ]
Stolnik, Snow
Thurecht, Kristofer J. [5 ]
Howdle, Steven M. [1 ,2 ]
Alexander, Cameron [1 ]
机构
[1] Univ Nottingham, Sch Pharm, Nottingham NG7 2RD, England
[2] Univ Nottingham, Sch Chem, Nottingham NG7 2RD, England
[3] Natl Univ Ireland, Network Excellence Funct Biomat, Galway, Ireland
[4] Ain Shams Univ, Fac Pharm, Dept Pharmaceut, Cairo, Egypt
[5] Univ Queensland, AIBN, Brisbane, Qld 4072, Australia
基金
英国工程与自然科学研究理事会;
关键词
TRANSFER RADICAL POLYMERIZATION; POLY(D; L-LACTIC-CO-GLYCOLIC ACID) MICROSPHERES; POLYION COMPLEX MICELLES; PLASMID DNA DELIVERY; DRUG-DELIVERY; BLOCK-COPOLYMERS; CLICK CHEMISTRY; IN-VIVO; BIOLOGICAL CHARACTERIZATION; POLY(ETHYLENE GLYCOL);
D O I
10.1021/bc100149g
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Multifunctional and modular block copolymers prepared from biocompatible monomers and linked by a bioreducible disulfide linkage have been prepared using a combination of ring-opening and atom-transfer radical polymerizations (ATRP). The presence of terminal functionality via ATRP allowed cell-targeting folic acid groups to be attached in a controllable manner, while the block copolymer architecture enabled well-defined nanoparticles to be prepared by a water-oil-water double emulsion procedure to encapsulate DNA with high efficiency. Gene delivery assays in a Calu-3 cell line indicated specific folate-receptor-mediated uptake of the nanoparticles, and triggered release of the DNA payload via cleavage of the disulfide link resulted in enhanced transgene expression compared to nonbioreducible analogues. These materials offer a promising and generic means to deliver a wide variety of therapeutic payloads to cells in a selective and tunable way.
引用
收藏
页码:156 / 168
页数:13
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