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Development and characterization of multifunctional nanoparticles for drug delivery to cancer cells.

机译:用于药物递送至癌细胞的多功能纳米颗粒的开发和表征。

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摘要

Lipid and polymeric nanoparticles, although proven to be effective drug delivery systems compared to free drugs, have shown considerable limitations pertaining to their uptake and release at tumor sites. Spatial and temporal control over the delivery of anticancer drugs has always been challenge to drug delivery scientists. Here, we have developed and characterized multifunctional nanoparticles (liposomes and polymersomes) which are targeted specifically to cancer cells, and release their contents with tumor specific internal triggers. To enable these nanoparticles to be tracked in blood circulation, we have imparted them with echogenic characteristic. Echogenicity of nanoparticles is evaluated using ultrasound scattering and imaging experiments. Nanoparticles demonstrated effective release with internal triggers such as elevated levels of MMP-9 enzyme found in the extracellular matrix of tumor cells, decreased pH of lysosome, and differential concentration of reducing agents in cytosol of cancer cells. We have also successfully demonstrated the sensitivity of these particles towards ultrasound to further enhance the release with internal triggers. To ensure the selective uptake by folate receptor- overexpressing cancer cells, we decorated these nanoparticles with folic acid on their surface. Fluorescence microscopic images showed significantly higher uptake of folate-targeted nanoparticles by MCF-7 (breast cancer) and PANC-1 (pancreatic cancer) cells compared to particles without any targeting ligand on their surface. To demonstrate the effectiveness of these nanoparticles to carry the drugs inside and kill cancer cells, we encapsulated doxorubicin and/or gemcitabine employing the pH gradient method. Drug loaded nanoparticles showed significantly higher killing of the cancer cells compared to their non-targeted counterparts and free drugs. With further development, these nanoparticles certainly have potential to be used as a multifunctional nanocarriers for image guided, targeted delivery of anticancer drugs.
机译:尽管与游离药物相比,脂质和聚合物纳米颗粒虽然被证明是有效的药物递送系统,但它们在肿瘤部位的摄取和释放方面显示出相当大的局限性。对抗癌药物的递送进行时空控制一直是药物递送科学家所面临的挑战。在这里,我们已经开发并表征了多功能纳米颗粒(脂质体和聚合体),这些纳米颗粒专门针对癌细胞,并通过肿瘤特异性内部触发物释放它们的内含物。为了使这些纳米颗粒能够在血液循环中被追踪,我们赋予了它们回声特性。使用超声散射和成像实验评估纳米粒子的致电子性。纳米粒子具有内部触发机制,例如在肿瘤细胞胞外基质中发现的MMP-9酶水平升高,溶酶体的pH降低以及癌细胞胞浆中还原剂的浓度不同,从而具有有效的释放作用。我们还成功地证明了这些颗粒对超声的敏感性,以进一步增强内部触发的释放。为了确保通过叶酸受体过表达的癌细胞选择性摄取,我们在这些纳米颗粒的表面修饰了叶酸。荧光显微图像显示,与在表面上没有任何靶向配体的颗粒相比,MCF-7(乳腺癌)和PANC-1(胰腺癌)细胞对叶酸靶向的纳米颗粒的摄取明显更高。为了证明这些纳米颗粒将药物携带到体内并杀死癌细胞的有效性,我们采用pH梯度法封装了阿霉素和/或吉西他滨。与未靶向的对应物和游离药物相比,载有药物的纳米颗粒对癌细胞的杀伤力明显更高。随着进一步的发展,这些纳米颗粒肯定有潜力用作多功能纳米载体,用于图像引导,靶向递送抗癌药物。

著录项

  • 作者

    Nahire, Rahul Rajaram.;

  • 作者单位

    North Dakota State University.;

  • 授予单位 North Dakota State University.;
  • 学科 Pharmaceutical sciences.;Biochemistry.;Nanotechnology.;Biomedical engineering.;Oncology.
  • 学位 Ph.D.
  • 年度 2014
  • 页码 170 p.
  • 总页数 170
  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类
  • 关键词

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