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Cell-Penetrating Magnetic Nanoparticles for Highly Efficient Delivery and Intracellular Imaging of siRNA

机译:穿透细胞的磁性纳米粒子用于siRNA的高效递送和细胞内成像

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摘要

RNA interference is one of the most promising technologies for cancer therapeutics, while the development of a safe and effective small interfering RNA (siRNA) delivery system is still challenging. Here, amphipol polymer and protamine peptide were employed to modify magnetic nanoparticles to form cell-penetrating magnetic nanoparticles (CPMNs). The unique CPMN could efficiently deliver the eGFP siRNA intracellularly and silence the eGFP expression in Cancer cells, which was verified by fluorescent imaging of cancer cells. Compared with lipofectamine and polyethyleneimine (PEI), CPMNs showed superior silencing efficiency and biocompatibility with minimum siRNA concentration as 5 nm in serum-containing medhim. CPMN was proved to be an efficient siRNA delivery system, which will have great potential in applications as a universal transmembrane carrier for intracellular gene delivery and simultaneous MRI imaging.
机译:RNA干扰是用于癌症治疗的最有前途的技术之一,而开发安全有效的小干扰RNA(siRNA)递送系统仍然是一项挑战。在这里,两亲聚合物和鱼精蛋白肽被用来修饰磁性纳米粒子,以形成穿透细胞的磁性纳米粒子(CPMNs)。独特的CPMN可以有效地在细胞内递送eGFP siRNA,并沉默癌细胞中eGFP的表达,这已通过癌细胞的荧光成像得到证实。与脂转染胺和聚乙烯亚胺(PEI)相比,CPMN在含有血清的二甲双胍中显示出优异的沉默效率和生物相容性,且最小siRNA浓度为5 nm。 CPMN被证明是一种有效的siRNA传递系统,作为细胞内基因传递和同步MRI成像的通用跨膜载体,在应用中将具有巨大的潜力。

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