Zhang Ling, Nguyen T L Uyen, Bernard Julien, Davis Thomas P, Barner-Kowollik Christopher, Stenzel Martina H
Centre for Advanced Macromolecular Design (CAMD), School of Chemical Sciences and Engineering, The University of New South Wales, Sydney, NSW 2052, Australia.
Biomacromolecules. 2007 Sep;8(9):2890-901. doi: 10.1021/bm070370g. Epub 2007 Aug 11.
Block copolymers poly(2-(dimethylamino) ethyl methacrylate)-b-poly(polyethylene glycol methacrylate) (PDMAEMA-b-P(PEGMA)) were prepared via reversible addition fragmentation chain transfer polymerization (RAFT). The polymerization was found to proceed with the expected living behavior resulting in block copolymers with varying block sizes of low polydispersity (PDI <1.3). The resulting block copolymer was self-assembled in an aqueous environment, leading to the formation of pH-responsive micelles. Further stabilization of the micellar system was performed in water using ethylene glycol dimethacrylate and the RAFT process to cross-link the shell. The cross-linked micelle was found to have properties significantly different from those of the uncross-linked block copolymer micelle. While a distinct critical micelle concentration (CMC) was observed using block copolymers, the CMC was absent in the cross-linked system. In addition, a better stability against disintegration was observed when altering the ionic strength such as the absence of changes of the hydrodynamic diameter with increasing NaCl concentration. Both cross-linked and uncross-linked micelles displayed good binding ability for genes. However, the cross-linked system exhibited a slightly superior tendency to bind oligonucleotides. Cytotoxicity tests confirmed a significant improvement of the biocompatibility of the synthesized cross-linked micelle compared to that of the highly toxic PDMAEMA. The cross-linked micelles were taken up by cells without causing any signs of cell damage, while the PDMAEMA homopolymer clearly led to cell death.
通过可逆加成-断裂链转移聚合(RAFT)制备了嵌段共聚物聚(甲基丙烯酸2-(二甲氨基)乙酯)-b-聚(甲基丙烯酸聚乙二醇酯)(PDMAEMA-b-P(PEGMA))。发现该聚合反应以预期的活性行为进行,得到具有不同嵌段尺寸且多分散性低(PDI<1.3)的嵌段共聚物。所得嵌段共聚物在水性环境中自组装,导致形成pH响应性胶束。使用乙二醇二甲基丙烯酸酯和RAFT工艺在水中对胶束体系进行进一步稳定化处理,以使壳交联。发现交联胶束具有与未交联的嵌段共聚物胶束显著不同的性质。使用嵌段共聚物时观察到明显的临界胶束浓度(CMC),而在交联体系中不存在CMC。此外,当改变离子强度时,例如随着NaCl浓度增加流体动力学直径没有变化,观察到对崩解具有更好的稳定性。交联和未交联的胶束对基因均显示出良好的结合能力。然而,交联体系显示出结合寡核苷酸的趋势略优。细胞毒性测试证实,与剧毒的PDMAEMA相比,合成的交联胶束的生物相容性有显著改善。交联胶束被细胞摄取而不会引起任何细胞损伤迹象,而PDMAEMA均聚物明显导致细胞死亡。