Suppr超能文献

隐形肟醚脂质体促进功能性 DsiRNA 在荷人肺癌 A549 肿瘤异种移植鼠中的传递。

Stealth oxime ether lipid vesicles promote delivery of functional DsiRNA in human lung cancer A549 tumor bearing mouse xenografts.

机构信息

RNA Structure and Design Section, RNA Biology Laboratory, NCI-NIH, Frederick, MD, United States of America.

RNA Structure and Design Section, RNA Biology Laboratory, NCI-NIH, Frederick, MD, United States of America; Department of Chemistry, University of Louisville, Louisville, KY, United States of America.

出版信息

Nanomedicine. 2022 Aug;44:102572. doi: 10.1016/j.nano.2022.102572. Epub 2022 Jun 4.

Abstract

We previously reported that hydroxylated oxime ether lipids (OELs) efficiently deliver functional Dicer substrate siRNAs (DsiRNAs) in cells. Here, we explored in vivo utility of these OELs, using OEL4 as a prototype and report that surface modification of the OEL4 formulations was essential for their in vivo applications. These surface-modified OEL4 formulations were developed by inclusion of various PEGylated lipids. The vesicle stability and gene knock-down were dependent on the PEG chain length. OEL4 containing DSPE-PEG350 and DSPE-PEG1000 (surprisingly not DSPE2000) promoted gene silencing in cells. In vivo studies demonstrated that OEL4 vesicles formulated using 3 mol% DSPE-PEG350 accumulate in human lung cancer (A549-luc2) xenografts in mice and exhibit a significant increase in tumor to liver ratios. These vesicles also showed a statistically significant reduction of luciferase signal in tumors compared to untreated mice. Taken together, the scalable OEL4:DSPE-PEG350 formulation serves as a novel candidate for delivery of RNAi therapeutics.

摘要

我们之前曾报道,羟基肟醚脂质(OEL)能够有效地将功能性 Dicer 底物 siRNA(DsiRNA)递送到细胞中。在这里,我们探索了这些 OEL 在体内的应用,选用 OEL4 作为原型,并报告说 OEL4 制剂的表面修饰对于其体内应用是必不可少的。通过包含各种聚乙二醇化脂质来开发这些经表面修饰的 OEL4 制剂。囊泡稳定性和基因敲低取决于 PEG 链长。含有 DSPE-PEG350 和 DSPE-PEG1000(令人惊讶的是不含 DSPE2000)的 OEL4 能够促进细胞中的基因沉默。体内研究表明,在小鼠的人肺癌(A549-luc2)异种移植瘤中,使用 3mol% DSPE-PEG350 制备的 OEL4 囊泡积聚,并显著增加肿瘤与肝脏的比值。与未治疗的小鼠相比,这些囊泡还使肿瘤中的荧光素酶信号显著降低。综上所述,可规模化的 OEL4:DSPE-PEG350 制剂是一种新型 RNAi 治疗药物递送候选物。

相似文献

本文引用的文献

1
Non-cationic Material Design for Nucleic Acid Delivery.用于核酸递送的非阳离子材料设计
Adv Ther (Weinh). 2020 Mar;3(3). doi: 10.1002/adtp.201900206. Epub 2020 Feb 13.
6
Nanoparticle-siRNA: A potential strategy for rheumatoid arthritis therapy?纳米颗粒-siRNA:类风湿关节炎治疗的潜在策略?
J Control Release. 2020 Sep 10;325:380-393. doi: 10.1016/j.jconrel.2020.07.006. Epub 2020 Jul 10.

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验