Lee Seung Koo, Tung Ching-Hsuan
Department of Translational Imaging, The Methodist Hospital Research Institute, Weill Cornell Medical College, Houston, TX 77030 (USA).
Adv Funct Mater. 2013 Jul 26;23(28):3488-3493. doi: 10.1002/adfm.201202777.
Persistent gene silencing is crucially required for the successful therapeutics of short interfering RNA (siRNA). Here, we describe a nanoparticle based delivery system which assembled by layering siRNAs between protease degradable polypeptides to extend the therapeutic window. These tightly packed nanoparticles are efficiently taken up by cells by endocytosis, and the fabricated siRNAs are gradually released following intracellular degradation of the polypeptide layers. During cell division, the particles are distributed to the daughter cells. Due to the slow degradation through the multiple layers, the particles continuously release siRNA in all cells. Using this controlled release construct, the gene silencing effect of siRNA is consistent for an ultra-long period of time (>3 weeks) with only a single treatment.
持续的基因沉默对于短干扰RNA(siRNA)的成功治疗至关重要。在此,我们描述了一种基于纳米颗粒的递送系统,该系统通过在蛋白酶可降解多肽之间分层siRNA来组装,以延长治疗窗口。这些紧密堆积的纳米颗粒通过内吞作用被细胞有效摄取,并且在多肽层细胞内降解后,制备的siRNA会逐渐释放。在细胞分裂期间,颗粒会分布到子细胞中。由于多层的缓慢降解,颗粒在所有细胞中持续释放siRNA。使用这种控释构建体,仅单次治疗,siRNA的基因沉默效果就能在超长时间(>3周)内保持一致。
Adv Funct Mater. 2013-7-26
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