有吸引力的药物递送方法:siRNA靶向的生物基载体

Zulal Yalinca, S. Tüzmen
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引用次数: 1

摘要

基因的功能特征可以通过基因表达的破坏来确定。这为设计新的治疗策略提供了强有力的方法。RNA干扰(RNAi)是一种有助于研究基因转录后调控的自然现象。这种机制可以通过在细胞中引入双链RNA(dsRNA)来刺激。合成的短/小干扰RNA(siRNA)可用于通过转染哺乳动物细胞来触发所需基因的下调。最近,利用生物基聚合物已经成为一种有吸引力的药物输送方法,用于医疗应用。这篇综述文章描述了利用生物基聚合物载体靶向siRNA作为生物疗法的优势。在此,我们报道了生物基siRNA的最新发展、安全性和通过聚合物载体的递送。此外,与临床应用进展有关的癌症遗传和代谢疾病,包括肥胖和糖尿病也得到了强调。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
ATTRACTIVE APPROACHES in DRUG DELIVERY: BIO-BASED CARRIERS for siRNA TARGETING
Functional characterization of genes can be determined by disruption of gene expression. This provides powerful approach in designing novel treatment strategies. RNA interference (RNAi) is a natural phenomenon that can aid in the study of post-transcriptional regulation of genes. This mechanism can be stimulated via introduction of double stranded RNA (dsRNA) in a cell. Synthetic short/small interfering RNAs (siRNA) can be utilized to trigger down-regulation of desired genes via transfecting into mammalian cells. Recently, utilization of bio-based polymers has been an attractive approach in drug delivery for medical applications. This review article describes the advantages of exploiting bio-based polymeric carriers for siRNA targeting, as bio-therapeutics. Here, we report the current developments, safety and delivery of bio-based siRNAs via polymeric carriers. Additionally, cancer genetics and metabolic disorders including obesity and diabetes pertaining to the progress in clinical applications have been highlighted.
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