...
首页> 外文期刊>Biomaterials >A reducible polycationic gene vector derived from thiolated low molecular weight branched polyethyleneimine linked by 2-iminothiolane.
【24h】

A reducible polycationic gene vector derived from thiolated low molecular weight branched polyethyleneimine linked by 2-iminothiolane.

机译:一种可还原的聚阳离子基因载体,由2-亚氨基硫杂环戊烷连接的硫醇化低分子量分支聚乙烯亚胺衍生而来。

获取原文
获取原文并翻译 | 示例

摘要

To improve transfection efficiency and reduce the cytotoxicity of polymeric gene vectors, reducible polycations (RPC) were synthesized from low molecular weight (MW) branched polyethyleneimine (bPEI) via thiolation and oxidation. RPC (RPC-bPEI(0.8 kDa)) possessed MW of 5 kDa-80 kDa, and 50%-70% of the original proton buffering capacity of bPEI(0.8 kDa) was preserved in the final product. The cytotoxicity of RPC-bPEI(0.8 kDa) was 8-19 times less than that of the gold standard of polymeric transfection reagents, bPEI(25 kDa). Although bPEI(0.8 kDa) exhibited poor gene condensing capacities ( approximately 2 mum at a weight ratio (WR) of 40), RPC-bPEI(0.8 kDa) effectively condensed plasmid DNA (pDNA) at a WR of 2. Moreover, RPC-bPEI(0.8 kDa)/pDNA (WR >/=2) formed 100-200 nm-sized particles with positively charged surfaces (20-35 mV). In addition, the results of the present study indicated that thiol/polyanions triggered the release of pDNA from RPC-bPEI(0.8 kDa)/pDNA via the fragmentation of RPC-bPEI(0.8 kDa) and ion-exchange. With negligible polyplex-mediated cytotoxicity, the transfection efficiencies of RPC-bPEI(0.8 kDa)/pDNA were approximately 1200-1500-fold greater than that of bPEI(0.8 kDa)/pDNA and were equivalent or superior ( approximately 7-fold) to that of bPEI(25 kDa)/pDNA. Interestingly, the distribution of high MW RPC-bPEI(0.8 kDa)/pDNA in the nucleus of the cell was higher than that of low MW RPC-bPEI(0.8 kDa)/pDNA. Thus, the results of the present study suggest that RPC-bPEI(0.8 kDa) has the potential to effectively deliver genetic materials with lower levels of toxicity.
机译:为了提高转染效率并降低聚合基因载体的细胞毒性,通过低分子量(MW)支链聚乙烯亚胺(bPEI)的硫醇化和氧化反应合成了可还原的聚阳离子(RPC)。 RPC(RPC-bPEI(0.8 kDa))的分子量为5 kDa-80 kDa,最终产品中保留了bPEI(0.8 kDa)原始质子缓冲能力的50%-70%。 RPC-bPEI(0.8 kDa)的细胞毒性比聚合转染试剂的金标准bPEI(25 kDa)低8-19倍。尽管bPEI(0.8 kDa)表现出较弱的基因浓缩能力(重量比(WR)为40时约为2毫米),但是RPC-bPEI(0.8 kDa)在WR为2时有效地浓缩了质粒DNA(pDNA)。 bPEI(0.8 kDa)/ pDNA(WR> / = 2)形成100-200 nm大小的带正电表面(20-35 mV)的颗粒。此外,本研究结果表明,巯基/聚阴离子通过RPC-bPEI(0.8 kDa)的片段化和离子交换触发了RPC-bPEI(0.8 kDa)/ pDNA的pDNA释放。由于多聚体介导的细胞毒性可忽略不计,RPC-bPEI(0.8 kDa)/ pDNA的转染效率比bPEI(0.8 kDa)/ pDNA的转染效率高约1200-1500倍,并且与bPEI(0.8 kDa)/ pDNA相当或优于(约7倍) bPEI(25 kDa)/ pDNA的。有趣的是,高MW RPC-bPEI(0.8 kDa)/ pDNA在细胞核中的分布高于低MW RPC-bPEI(0.8 kDa)/ pDNA。因此,本研究的结果表明,RPC-bPEI(0.8 kDa)具有有效递送具有较低毒性水平的遗传物质的潜力。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号