Department of Pharmaceutics and Biopharmacy, Philipps-Universität, Marburg, Germany.
Pharm Res. 2010 Dec;27(12):2670-82. doi: 10.1007/s11095-010-0266-8. Epub 2010 Sep 17.
The objective of this study was to investigate how the degree of amine substitution of amine-modified poly(vinyl alcohol) (PVA) affects complexation of siRNA, protection of siRNA against degrading enzymes, intracellular uptake and gene silencing.
A series of DEAPA-PVA polymers with increasing amine density was synthesized by modifying the hydroxyl groups in the PVA backbone with diethylamino propylamine groups using CDI chemistry. These polymers were characterized with regard to their ability to complex and protect siRNA against RNase. Finally, their potential to mediate intracellular uptake and gene silencing in SKOV-luc cells was investigated.
A good correlation between amine density and siRNA complexation as well as protection of siRNA against RNase was found. Consisting solely of tertiary amines, this class of polymer was able to mediate efficient gene silencing when approximately 30% of the hydroxyl groups in the PVA backbone were modified with diethylamino propylamine groups. Polymers with a lower amine density (up to 23%) were inefficient in gene silencing, while increasing the amine density to 48% led to non-specific knockdown effects.
DEAPA-PVA polymers were shown to mediate efficient gene silencing and offer a promising platform for further structural modifications.
本研究旨在探讨胺基取代度对胺基改性聚乙烯醇(PVA)与 siRNA 复合物形成、保护 siRNA 免受降解酶影响、细胞内摄取和基因沉默的影响。
采用 CDI 化学方法,用二乙基氨基丙基胺基团修饰 PVA 主链上的羟基,合成一系列胺基密度逐渐增加的 DEAPA-PVA 聚合物。对这些聚合物与 siRNA 复合及保护 siRNA 免受 RNase 降解的能力进行了表征。最后,研究了它们在 SKOV-luc 细胞中介导细胞内摄取和基因沉默的潜力。
发现胺基密度与 siRNA 复合以及保护 siRNA 免受 RNase 降解之间存在良好的相关性。这类聚合物完全由叔胺组成,当 PVA 主链上约 30%的羟基被二乙基氨基丙基胺基团修饰时,能够介导有效的基因沉默。胺基密度较低(低至 23%)的聚合物在基因沉默方面效率较低,而增加胺基密度至 48%则会导致非特异性的基因敲低效应。
DEAPA-PVA 聚合物被证明能有效介导基因沉默,并为进一步的结构修饰提供了有前途的平台。