首页> 外文期刊>Pharmaceutical research >Disulfide-based poly(amido amine)s for siRNA delivery: effects of structure on siRNA complexation, cellular uptake, gene silencing and toxicity.
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Disulfide-based poly(amido amine)s for siRNA delivery: effects of structure on siRNA complexation, cellular uptake, gene silencing and toxicity.

机译:用于siRNA递送的基于二硫键的聚(酰胺胺):结构对siRNA络合,细胞摄取,基因沉默和毒性的影响。

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摘要

PURPOSE: RNA interference (RNAi) is a process by which small interfering RNAs (siRNA) induce sequence-specific gene silencing. Therefore, siRNA is an emerging promise as a novel therapeutic. In order to realize the high expectations for therapeutic applications, efficient delivery systems for siRNA are necessary. METHODS: In this study, a new series of biodegradable poly(amido amine)s with disulfide linkages in the backbone was synthesized out of N,N'-cystaminebisacrylamide (CBA), 4-amino-1-butanol (ABOL) and ethylene diamine (EDA). Effects of different percentages of butanolic side chains and protonatable fragments in the main chain on siRNA complexation, cellular uptake, gene silencing and toxicity were investigated. RESULTS: Incorporation of EDA in the polymer resulted in increased siRNA condensation. Efficient siRNA condensation was shown to be necessary for cellular uptake; however, excess of polymer decreased siRNA uptake for polymers with high amounts of EDA. Silencing efficiency did not correlate with uptake, since silencing increased with increasing w/w ratio for all polymers. More than 80% knockdown was found for polyplexes formed with polymers containing 25% or 50% EDA, which was combined with low cytotoxicity. CONCLUSIONS: Poly(amido amine)s with minor fractions of protonatable fragments in the main chain are promising carriers for delivery of siRNA.
机译:目的:RNA干扰(RNAi)是小干扰RNA(siRNA)诱导序列特异性基因沉默的过程。因此,siRNA作为一种新型治疗剂正在崭露头角。为了实现对治疗应用的高度期望,需要有效的siRNA递送系统。方法:在这项研究中,合成了一系列在主链上具有二硫键的可生物降解的聚(酰胺基胺),它们是由N,N'-胱胺双丙烯酰胺(CBA),4-氨基-1-丁醇(ABOL)和乙二胺合成的(EDA)。研究了不同百分比的丁醇侧链和主链中质子化片段对siRNA络合,细胞摄取,基因沉默和毒性的影响。结果:在聚合物中加入EDA导致siRNA缩合增加。研究表明有效的siRNA浓缩对于细胞摄取是必要的。但是,过量的聚合物会降低具有大量EDA的聚合物的siRNA吸收。沉默效率与摄取不相关,因为所有聚合物的沉默随着w / w比的增加而增加。对于由包含25%或50%EDA的聚合物形成的多链体,发现多态性超过80%,且细胞毒性低。结论:在主链中具有少量可质子化片段的聚(酰胺胺)是有希望的传递siRNA的载体。

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