首页> 外文期刊>RSC Advances >Co-delivery of drug nanoparticles and siRNA mediated by a modified cell penetrating peptide for inhibiting cancer cell proliferation
【24h】

Co-delivery of drug nanoparticles and siRNA mediated by a modified cell penetrating peptide for inhibiting cancer cell proliferation

机译:修饰的细胞穿透肽介导的药物纳米颗粒和siRNA的共递送抑制癌细胞增殖

获取原文
获取原文并翻译 | 示例
           

摘要

Co-delivery of anti-cancer agent Ellipticine (EPT) and Bcl-2 siRNA was mediated by a modified cell penetrating peptide, stearylated H16R8 (STR-H16R8). The stability and efficacy of the EPT nanoparticles was improved significantly by the amphiphilic peptide. Efficacy of STR-H16R8 stabilized EPT nanoparticles was further enhanced with Bcl-2 siRNA.
机译:抗癌药玫瑰树碱(EPT)和Bcl-2 siRNA的共同传递是通过修饰的细胞穿透肽硬脂酸化H16R8(STR-H16R8)介导的。两亲性肽显着提高了EPT纳米颗粒的稳定性和功效。 Bcl-2 siRNA进一步增强了STR-H16R8稳定的EPT纳米颗粒的功效。

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