首页> 外文OA文献 >Layer-by-Layer Nanoparticles for Systemic Codelivery of an Anticancer Drug and siRNA for Potential Triple-Negative Breast Cancer Treatment
【2h】

Layer-by-Layer Nanoparticles for Systemic Codelivery of an Anticancer Drug and siRNA for Potential Triple-Negative Breast Cancer Treatment

机译:逐层纳米粒子用于抗癌药物的系统编码和用于潜在三阴性乳腺癌治疗的siRNa

代理获取
本网站仅为用户提供外文OA文献查询和代理获取服务,本网站没有原文。下单后我们将采用程序或人工为您竭诚获取高质量的原文,但由于OA文献来源多样且变更频繁,仍可能出现获取不到、文献不完整或与标题不符等情况,如果获取不到我们将提供退款服务。请知悉。

摘要

A single nanoparticle platform has been developed through the modular and controlled layer-by-layer process to codeliver siRNA that knocks down a drug-resistance pathway in tumor cells and a chemotherapy drug to challenge a highly aggressive form of triple-negative breast cancer. Layer-by-layer films were formed on nanoparticles by alternately depositing siRNA and poly-l-arginine; a single bilayer on the nanoparticle surface could effectively load up to 3500 siRNA molecules, and the resulting LbL nanoparticles exhibit an extended serum half-life of 28 h. In animal models, one dose via intravenous administration significantly reduced the target gene expression in the tumors by almost 80%. By generating the siRNA-loaded film atop a doxorubicin-loaded liposome, we identified an effective combination therapy with siRNA targeting multidrug resistance protein 1, which significantly enhanced doxorubicin efficacy by 4 fold in vitro and led to up to an 8-fold decrease in tumor volume compared to the control treatments with no observed toxicity. The results indicate that the use of layer-by-layer films to modify a simple liposomal doxorubicin delivery construct with a synergistic siRNA can lead to significant tumor reduction in the cancers that are otherwise nonresponsive to treatment with Doxil or other common chemotherapy drugs. This approach provides a potential strategy to treat aggressive and resistant cancers, and a modular platform for a broad range of controlled multidrug therapies customizable to the cancer type in a singular nanoparticle delivery system.
机译:通过模块化和受控的逐层过程开发了单个纳米粒子平台,以编码传递siRNA的siRNA,敲低肿瘤细胞中的耐药性途径和化学疗法药物以挑战高度侵袭性的三阴性乳腺癌。通过交替沉积siRNA和聚-1-精氨酸在纳米颗粒上形成一层一层的膜。纳米颗粒表面上的单个双层可以有效装载多达3500个siRNA分子,并且所得的LbL纳米颗粒具有28 h的延长的血清半衰期。在动物模型中,通过静脉内给药一剂可将肿瘤中的靶基因表达显着降低近80%。通过在载有阿霉素的脂质体上生成载有siRNA的膜,我们确定了与靶向多药耐药蛋白1的siRNA的有效联合疗法,该药物显着提高了阿霉素的体外功效4倍,并导致肿瘤减少多达8倍与对照治疗相比,没有观察到毒性。结果表明,使用层状膜修饰具有协同siRNA的简单脂质体阿霉素递送构建体可导致癌症的明显减少,这些癌症对使用Doxil或其他常见化学疗法的治疗无反应。这种方法提供了一种治疗侵袭性和耐药性癌症的潜在策略,并提供了一种模块化平台,可用于在单个纳米颗粒递送系统中针对癌症类型进行定制的多种受控多药疗法。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
代理获取

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