首页> 美国卫生研究院文献>Scientific Reports >Fabrication characterization and biological evaluation of anti-HER2 indocyanine green-doxorubicin-encapsulated PEG-b-PLGA copolymeric nanoparticles for targeted photochemotherapy of breast cancer cells
【2h】

Fabrication characterization and biological evaluation of anti-HER2 indocyanine green-doxorubicin-encapsulated PEG-b-PLGA copolymeric nanoparticles for targeted photochemotherapy of breast cancer cells

机译:抗HER2吲哚菁绿-阿霉素包裹的PEG-b-PLGA共聚纳米粒的制备表征和生物学评价用于乳腺癌细胞的靶向光化学疗法

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

In this study, we aimed to develop anti-human epidermal growth factor receptor 2 (HER2) indocyanine green (ICG)-doxorubicin (DOX)-encapsulated polyethylene glycol-poly(lactic-co-glycolic acid) diblock copolymeric nanoparticles (HIDPPNPs) to explore the co-administration of phototherapy and chemotherapy for HER2-overexpressing breast cancer, a highly aggressive and medicine-resistant breast carcinoma. The HIDPPNPs were fabricated using a solvent evaporation technique followed by carbodiimide-mediated antibody conjugation on the nanoparticle surface. Compared with freely dissolved ICG, the HIDPPNPs conferred enhanced thermal stability to the entrapped ICG, were able to generate a hyperthermia effect at concentrations ≥1 μM ICG equivalent and provided increased production of singlet oxygen under 808-nm laser irradiation with an intensity of 6 W/cm2. Furthermore, the uptake efficiency of the HIDPPNPs in MDA-MB-453/HER2(+) cells was approximately 2-fold higher than that in MCF7/HER2(−) cells, demonstrating that the HIDPPNPs specifically target HER2-expressing cells. Based on the viability analysis, the HIDPPNPs exhibited effective cytotoxicity upon light exposure (808 nm; 6 W/cm2), and the resulting cell death rate was even higher than that caused by using twice amount of encapsulated DOX or ICG alone. These results indicate that the developed HIDPPNPs may serve as a feasible tool for use in anti-HER2 breast cancer therapy with reduced chemotoxicity.
机译:在这项研究中,我们旨在开发抗人类表皮生长因子受体2(HER2)吲哚菁绿(ICG)-阿霉素(DOX)封装的聚乙二醇-聚乳酸-乙醇酸二嵌段共聚物纳米颗粒(HIDPPNPs),探索光疗和化学疗法共同治疗过度表达HER2的乳腺癌(一种高度侵袭性和耐药性的乳腺癌)的方法。使用溶剂蒸发技术,然后将碳二亚胺介导的抗体偶联在纳米颗粒表面上,制备HIDPPNP。与自由溶解的ICG相比,HIDPPNP赋予包裹的ICG更高的热稳定性,能够在浓度≥1μMICG当量的情况下产生热疗效果,并在强度为6 W的808 nm激光辐照下产生单线态氧的增加/ cm 2 。此外,MDA-MB-453 / HER2(+)细胞中HIDPPNP的吸收效率比MCF7 / HER2-(-)细胞中的HIDPPNP吸收效率高约2倍,这表明HIDPPNPs特异性靶向表达HER2的细胞。根据生存力分析,HIDPPNPs在暴露于光(808 nm; 6 W / cm 2 )时显示出有效的细胞毒性,并且所产生的细胞死亡率甚至比使用两倍量的包封所导致的细胞死亡率还要高。单独使用DOX或ICG。这些结果表明,已开发的HIDPPPNPs可以作为一种可行的工具用于化学毒性降低的抗HER2乳腺癌治疗。

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