Rational design of biodegradable cationic polycarbonates for gene delivery

被引:65
作者
Ong, Zhan Yuin [1 ,2 ]
Fukushima, Kazuki [3 ]
Coady, Daniel J. [3 ]
Yang, Yi-Yan [1 ]
Ee, Pui Lai Rachel [2 ]
Hedrick, James L. [3 ]
机构
[1] Inst Bioengn & Nanotechnol, Singapore 138669, Singapore
[2] Natl Univ Singapore, Dept Pharm, Singapore 117543, Singapore
[3] IBM Almaden Res Ctr, San Jose, CA 95120 USA
关键词
Cationic polymer; Polycarbonate; Organocatalysis; Ring-opening polymerization; Gene transfection; RING-OPENING POLYMERIZATION; DNA DELIVERY; BLOCK-COPOLYMERS; TRANSFECTION EFFICIENCY; TRIMETHYLENE CARBONATE; L-LACTIDE; IN-VITRO; POLYMERS; VECTORS; POLYETHYLENIMINE;
D O I
10.1016/j.jconrel.2011.01.020
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Polycarbonates provide an attractive option for use as gene delivery vectors owing to their biocompatibility and ease of incorporating functional moieties. In this study, we described an approach to synthesize cationic polymers with well-defined molecular weights and narrow polydispersities by an organocatalytic ring-opening polymerization of functional cyclic carbonates containing alkyl halide side chains, followed by a subsequent functionalization step with bis-tertiary amines designed to facilitate gene binding and endosomal escape. The cationic polycarbonate effectively condensed DNA at low N/P ratios, generating nanoparticles (83 to 124 nm in diameter) with positive zeta potentials (similar to 27 mV). In addition, reporter gene expression efficiencies in HepG2. HEK293, MCF-7 and 4T1 cell lines were high even in the presence of serum. Importantly, the polycarbonate delivery agent demonstrated minimal cytotoxicity at the optimal N/P ratios determined to confer high gene expression efficiencies. Therefore, this biodegradable polymer is presented as a promising non-viral vector for gene delivery. (C) 2011 Elsevier B.V. All rights reserved.
引用
收藏
页码:120 / 126
页数:7
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