首页> 外文期刊>Journal of nanotechnology >Organic Nanovesicular Cargoes for Sustained Drug Delivery: Synthesis, Vesicle Formation, Controlling 'Pearling' States, and Terfenadine Loading/Release Studies
【24h】

Organic Nanovesicular Cargoes for Sustained Drug Delivery: Synthesis, Vesicle Formation, Controlling 'Pearling' States, and Terfenadine Loading/Release Studies

机译:用于持续药物输送的有机纳米囊泡货物:合成,囊泡形成,控制“发皮”状态以及特非那定的负载/释放研究

获取原文
获取原文并翻译 | 示例
       

摘要

"Sustained drug delivery systems" which are designed to accomplish long-lasting therapeutic effect are one of the challenging topics in the area of nanomedicine. We developed an innovative strategy to prepare nontoxic and polymer stabilized organic nanovesicles (diameter: 200 nm) from a novel bolaamphiphile, where two hydrogen bonding acetyl cytosine molecules connected to 4,4″-positions of the 2,6-bispyrazolylpyridine through two flexible octyne chains. The nanovesicles behave like biological membrane by spontaneously self-assembling into "pearl-like" chains and subsequently forming long nanotubes (diameter: 150 nm), which further develop into various types of network-junctions through self-organization. For drug loading and delivery applications, the nanovesicles were externally protected with biocompatible poly(ethyleneglycol) -2000 to prevent them from fusion and ensuing tube formation. Nontoxic nature of the nanovesicles was demonstrated by zebrafish teratogenicity assay. Biocompatible nanovesicles were loaded with "terfenadine" drug and successfully utilized to transport and release drug in sustained manner (up to 72 h) in zebrafish larvae, which is recognized as an emerging in vivo model system.
机译:旨在实现持久治疗效果的“持续药物输送系统”是纳米医学领域中具有挑战性的主题之一。我们开发了一种创新策略,可以从新型的双亲亲亲分子中制备无毒且聚合物稳定的有机纳米囊泡(直径:200 nm),其中两个氢键合乙酰基胞嘧啶分子通过两个柔性辛炔连接到2,6-双吡唑基吡啶的4,4''-位链。纳米囊泡通过自发自组装成“珍珠状”链并随后形成长纳米管(直径:150 nm),表现得像生物膜一样,通过自组织进一步发展成各种类型的网络结。对于药物装载和递送应用,用生物相容性聚(乙二醇)-2000从外部保护纳米囊泡,以防止它们融合并随后形成管子。纳米囊泡的无毒性质已通过斑马鱼的致畸性试验得以证实。生物相容性纳米囊泡载有“ terfenadine”药物,并成功用于在斑马鱼幼虫中以持续方式(长达72小时)运输和释放药物,这被认为是一种新兴的体内模型系统。

著录项

  • 来源
    《Journal of nanotechnology》 |2014年第2014期|369139.1-369139.13|共13页
  • 作者单位

    Functional Molecular Nano/Micro Solids Laboratory, School of Chemistry, University of Hyderabad, Hyderabad 500046, India;

    Organic & Medicinal Chemistry, Reddy's Institute of Life Sciences, University of Hyderabad Campus, Hyderabad 500046, India;

    Organic & Medicinal Chemistry, Reddy's Institute of Life Sciences, University of Hyderabad Campus, Hyderabad 500046, India;

    Biology Department, Reddy's Institute of Life Sciences, University of Hyderabad Campus, Hyderabad 500046, India;

    Biology Department, Reddy's Institute of Life Sciences, University of Hyderabad Campus, Hyderabad 500046, India,Zephase Therapeutics, Reddy's Institute of Life Sciences, University of Hyderabad Campus, Hyderabad 500046, India;

    Functional Molecular Nano/Micro Solids Laboratory, School of Chemistry, University of Hyderabad, Hyderabad 500046, India;

    Organic & Medicinal Chemistry, Reddy's Institute of Life Sciences, University of Hyderabad Campus, Hyderabad 500046, India;

  • 收录信息
  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类
  • 关键词

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