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Polymeric micelles self-assembled from amphiphilic polymers with twin disulfides used as siRNA carriers to enhance the transfection

机译:聚合物胶束从两性二硫化物自组装,用双二硫化物用作siRNA载体,以增强转染

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摘要

The sequence-defined polycationic polymers with or without Cys-Arg-Cys motifs conjugated with targeting and shielding segments were synthesized as siRNA carriers via native chemical ligation (NCL) reaction. After purification, the structures and physicochemical characteristics were determined by a variety of experimental techniques. The particle size of siRNA/CRC-polymer polyplex was much smaller than that of polyplex without CRC motifs. The buffer capacity and siRNA binding ability of CRC motifs modified polymers were significantly improved, resulting from the twin disulfides and hexatomic ring formulation. The critical micelle concentrations of the polymers were <10 mg/L, indicating formation of polymeric micelles and sufficient stability of the system. The CRC motifs modified polymers with folate targeted ligands exhibited a strongly enhanced cellular uptake than the negative control and the unmodified analogues. The results of gene transfection showed that the folate-PEG-ligated polymer modified with CRC motifs had much better gene transfection compared to the alanine-ended control and other analogues. Furthermore, they showed barely cytotoxicity. By the way, there was no distinctly improvement for pDNA transfection. All above results suggested that folate-PEG-ligated polymers modified with CRC motifs and their self-assembly polymeric micelles could be promising non-viral siRNA carriers. (C) 2017 Elsevier B.V. All rights reserved.
机译:具有或不含Cys-Arg-Cys基序与靶向和屏蔽段缀合的Cys-Arg-Cys基序的序列定义的聚酰基聚合物通过天然化学连接(NCl)反应作为SiRNA载体合成。纯化后,通过各种实验技术确定结构和物理化学特性。没有CRC基序的SiRNA / CrC-聚合物多络合物的粒度远小于多分工。 CRC基序改性聚合物的缓冲能力和siRNA结合能力显着改善,由双二硫化物和六磷酸环制剂产生。聚合物的临界胶束浓度<10mg / L,表明聚合物胶束的形成以及该系统的充分稳定性。 CRC基序与叶酸靶向配体的聚合物的改性聚合物表现出比阴性对照和未改性类似物的强烈增强的细胞吸收。基因转染的结果表明,与丙氨酸结束的对照和其他类似物相比,用CRC基序改性的叶酸-PEG连接聚合物具有更好的基因转染。此外,它们显示出几乎没有细胞毒性。顺便说一下,PDNA转染没有明显改善。上述结果表明,用CRC基序和其自组装聚合物胶束改性的叶酸粘合剂连接聚合物可能是有前途的非病毒siRNA载体。 (c)2017 Elsevier B.v.保留所有权利。

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