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Stabilization of gold nanoparticles in organic solvents for use in drug delivery applications.

机译:金纳米颗粒在有机溶剂中的稳定化,用于药物递送应用。

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摘要

Gold nanoparticles (AuNP) are an excellent candidate for drug delivery vehicles due to their unique physical and chemical properties enabling the transport and subsequent release of payloads such as drugs or genetic materials to specific tissue sites. Their advantages include their ease of synthesis: monodisperse nanoparticles from 1 to 150 nm in size, the gold core is essentially inert and non-toxic, they can be readily functionalized by noncovalent interaction or via covalent chemical conjunction of drugs, and finally their release can be triggered via their photo-physical properties or mediated by intercellular glutathionefl, 2]. Active and passive targeting can be achieved by attaching ligands such as TNF (tumor necrosis factor), or proteins onto the nanoparticles or through size and charge effects [3, 4].
机译:金纳米颗粒(AuNP)由于其独特的物理和化学特性,使得诸如药物或遗传物质的有效载荷能够运输和随后释放到特定的组织部位,因此是药物输送载体的极佳候选者。它们的优点包括易于合成:尺寸为1至150 nm的单分散纳米颗粒,金核基本上是惰性的且无毒,可以通过非共价相互作用或药物的共价化学结合而容易地官能化,最后它们的释放可以通过它们的光物理特性触发或由细胞间谷胱甘肽介导[2]。可以通过将诸如TNF(肿瘤坏死因子)之类的配体或蛋白质附着到纳米颗粒上,或者通过大小和电荷效应来实现主动和被动靶向[3,4]。

著录项

  • 来源
  • 会议地点 Tampere(FI);Tampere(FI)
  • 作者

    J. Manson; D. Kumar; D. Dixon;

  • 作者单位

    University of Ulster, Jordanstown, N. Irealnd;

    University of Ulster, Jordanstown, N. Irealnd;

    University of Ulster, Jordanstown, N. Irealnd;

  • 会议组织
  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类 TB347;
  • 关键词

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