首页> 美国卫生研究院文献>Drug Delivery >Polydopamine-tailored paclitaxel-loaded polymeric microspheres with adhered NIR-controllable gold nanoparticles for chemo-phototherapy of pancreatic cancer
【2h】

Polydopamine-tailored paclitaxel-loaded polymeric microspheres with adhered NIR-controllable gold nanoparticles for chemo-phototherapy of pancreatic cancer

机译:贴有近红外可控金纳米粒子的聚多巴胺定制紫杉醇聚合物微球用于胰腺癌的化学光疗

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

Chemotherapeutic drugs often used as a first-line treatment of pancreatic cancer (PC) exhibit challenges due to resistance development, lack of selectivity, and tumor heterogeneity. Currently, combination chemo-photothermal therapy is known to enhance the therapeutic efficacy of chemotherapeutic drugs in PC. In this study, we develop adherent gold nanoparticles (GNPs) and paclitaxel (PTX)-loaded PLGA microspheres for the treatment of PC. Polydopamine (pD) was used as a linker to adhere GNPs to the surface of PLGA-Ms and characterized using TEM. Short-term cytotoxicity of GNPs-pD-PTX-PLGA-Ms with or without NIR treatment was evaluated using CCK-8 assays. ROS and western blot assay were performed to determine the intensity of ROS following the treatment of GNPs-pD-PTX-PLGA-Ms with or without NIR in Panc-1 cell line. Successful adhesion of GNPs on the microspheres was confirmed by TEM. CCK-8 assay revealed that GNPs-pD-PTX-PLGA-Ms with NIR showed three-fold higher cytotoxicity, compared to the group without NIR. Furthermore, ROS and western blot assay suggest that GNPs-pD-PTX-PLGA-Ms with NIR showed more ROS generation, followed by downregulation of the expression levels of antioxidant enzyme (SOD2 and CATALASE). These results suggest that the GNPs-pD-PTX-PLGA-Ms in combination with NIR irradiation can provide a synergistic chemo-photothermal therapy for the treatment of PC.
机译:由于抗药性的发展,缺乏选择性和肿瘤异质性,常被用作胰腺癌(PC)一线治疗的化学治疗药物面临挑战。目前,已知化学-光热联合疗法可增强化学治疗药物在PC中的治疗效果。在这项研究中,我们开发了粘附金纳米颗粒(GNP)和紫杉醇(PTX)负载的PLGA微球用于PC的治疗。聚多巴胺(pD)用作将GNP粘附到PLGA-Ms表面的连接子,并使用TEM进行了表征。使用CCK-8分析评估使用或不使用NIR治疗的GNP-pD-PTX-PLGA-Ms的短期细胞毒性。在Panc-1细胞系中处理带有或不带有NIR的GNPs-pD-PTX-PLGA-Ms后,进行ROS和Western blot分析以确定ROS的强度。 TEM证实了GNP在微球上的成功粘附。 CCK-8分析显示,与没有NIR的组相比,具有NIR的GNPs-pD-PTX-PLGA-Ms显示出高三倍的细胞毒性。此外,ROS和蛋白质印迹分析表明,具有NIR的GNPs-pD-PTX-PLGA-Ms显示出更多的ROS生成,随后下调了抗氧化酶(SOD2和CATALASE)的表达水平。这些结果表明,GNPs-pD-PTX-PLGA-Ms与NIR辐射结合可以为PC的治疗提供协同的化学光热疗法。

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