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Nanofibres Deliver Drug To Exact Spot

机译:纳米纤维将药物精确递送

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摘要

Stringing drug molecules into fibres that unravel in the presence of a specific enzyme could allow medication to be released exactly when and where it is needed.rnPreviously, drugs have been bundled with polymers that, once injected into a patient, slowly break down to release the drug. By tuning the properties of the polymer, this allows the timing of a drug's release to be pre-programmed. However, the polymers can release toxic molecules as they degrade.rnNow George John from the City University of New York and team have created a way to pre-program drug release without using potentially harmful polymers. In John's system, drugs are released in response to a specific enzyme, allowing where and when the release occurs to be controlled.rnThe team attached a "water-hating" fatty acid to the end ofrna "water-loving" drug molecule -in this case the painkiller paracetamol (acetaminophen). Because the water-hating fatty acid tails are attracted to each other, and the water-loving paracetamol heads to other heads, the molecules stack,rnwith the tails at the centre and the heads facing outwards, to form nanofibres that cluster together in a mesh (see Diagram).
机译:将药物分子串入在特定酶存在下解开的纤维中,可以使药物在需要的时间和地点准确释放。rn以前,药物与聚合物捆绑在一起,一旦注入患者体内,它就会缓慢分解以释放出药物。药品。通过调节聚合物的特性,可以对药物释放的时间进行预编程。但是,这些聚合物在降解时会释放出有毒分子。现在,纽约市大学的George John及其团队创造了一种无需使用潜在有害聚合物即可对药物释放进行预编程的方法。在约翰的系统中,药物是根据特定的酶释放的,从而可以控制释放的时间和地点。该团队在“爱水”药物分子的末端附加了“憎水”脂肪酸案例止痛药对乙酰氨基酚(对乙酰氨基酚)。由于憎水脂肪酸的尾巴相互吸引,而爱好水的扑热息痛则朝向其他头部,因此分子以尾巴居中且头部朝外的方式堆叠在一起,形成纳米纤维,这些纳米纤维聚集成网状(请参见图)。

著录项

  • 来源
    《New scientist》 |2009年第2689期|10|共1页
  • 作者

    DAVID ROBSON;

  • 作者单位
  • 收录信息 美国《科学引文索引》(SCI);美国《化学文摘》(CA);
  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类
  • 关键词

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