Department of Materials Science & Engineering, University of Washington, Seattle, WA 98195, USA.
Biomaterials. 2010 Nov;31(31):8032-42. doi: 10.1016/j.biomaterials.2010.07.016. Epub 2010 Jul 31.
Ribonucleic acid interference (RNAi) is a powerful molecular tool that has potential to revolutionize the treatment of cancer. One major challenge of applying this technology for clinical application is the lack of site-specific carriers that can effectively deliver short interfering RNA (siRNA) to cancer cells. Here we report the development and assessment of a cancer-cell specific magnetic nanovector construct for efficient siRNA delivery and non-invasive monitoring through magnetic resonance imaging (MRI). The base of the nanovector construct is comprised of a superparamagnetic iron oxide nanoparticle core coated with polyethylene glycol (PEG)-grafted chitosan, and polyethylenimine (PEI). The construct was then further functionalized with siRNA and a tumor-targeting peptide, chlorotoxin (CTX), to improve tumor specificity and potency. Flow cytometry, quantitative RT-PCR, and fluorescence microscopy analyses confirmed receptor-mediated cellular internalization of nanovectors and enhanced gene knockdown through targeted siRNA delivery. The ability of this nanovector construct to generate specific contrast enhancement of glioblastoma cells was demonstrated through MR imaging. These findings suggest that this CTX enabled nanoparticle carrier may be well suited for delivery of RNAi therapeutics to brain cancer cells.
核糖核酸干扰(RNAi)是一种强大的分子工具,有可能彻底改变癌症的治疗方法。将这项技术应用于临床应用的主要挑战之一是缺乏能够将短干扰 RNA(siRNA)有效递送到癌细胞的特异性载体。在这里,我们报告了一种用于高效 siRNA 递送和通过磁共振成像(MRI)进行非侵入性监测的癌症细胞特异性磁性纳米载体构建体的开发和评估。纳米载体构建体的基础由超顺磁性氧化铁纳米颗粒核心组成,该核心涂覆有聚乙二醇(PEG)接枝壳聚糖和聚乙烯亚胺(PEI)。然后,通过氯毒素(CTX)进一步对构建体进行功能化,以提高肿瘤特异性和效力。流式细胞术、定量 RT-PCR 和荧光显微镜分析证实了纳米载体的受体介导的细胞内吞作用,并通过靶向 siRNA 递送增强了基因敲低。通过磁共振成像证明了这种纳米载体构建体能够特异性增强脑胶质瘤细胞的对比度增强。这些发现表明,这种 CTX 赋予的纳米颗粒载体可能非常适合将 RNAi 治疗剂递送到脑癌细胞。