Center for Controlled Chemical Delivery, Department of Pharmaceutics and Pharmaceutical Chemistry, University of Utah, Salt Lake City, UT 84112, USA.
Macromol Biosci. 2010 Aug 11;10(8):898-905. doi: 10.1002/mabi.200900482.
Bioreducible cationic polymer poly(CBA-DAH) containing repeated disulfide linkages on the polymer backbone was synthesized through Michael-type polyadditions of CBA to DAH monomers. Poly(CBA-DAH) could spontaneously form nanoscale polyelectrolyte complexes through electrostatic interactions with siRNA in an aqueous phase. These nanoparticles were rapidly degraded under the reductive cytoplasmic environment with subsequently releasing the siRNA cargo into the cytoplasm where RNAi takes place, as a result of the breakdown of disulfide bonds in the polymers. The reductive degradation behavior of the poly(CBA-DAH)/siRNA polyplexes is more likely to increase RNAi activity with enhancing the cytoplasmic localization of siRNA molecules. Poly(CBA-DAH) may have great potential as a gene carrier especially for therapeutic applications of siRNAs owing to the reductive degradation characteristics.
具有重复二硫键的生物还原阳离子聚合物聚(CBA-DAH)通过 CBA 与 DAH 单体的迈克尔加成反应合成。聚(CBA-DAH)可以通过与水溶液中的 siRNA 之间的静电相互作用自发形成纳米级聚电解质复合物。这些纳米颗粒在还原性细胞质环境下迅速降解,随后将 siRNA 货物释放到细胞质中,从而发生 RNAi,这是由于聚合物中二硫键的断裂。聚(CBA-DAH)/siRNA 聚合物胶束的还原降解行为更有可能通过增强 siRNA 分子的细胞质定位来提高 RNAi 活性。聚(CBA-DAH)可能具有作为基因载体的巨大潜力,特别是对于 siRNA 的治疗应用,这归因于其还原降解特性。