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Cucurbitnuril type hosts for the reversal of steroidal neuromuscular blocking agents

机译:葫芦n脲型宿主,用于逆转甾体神经肌肉阻滞剂

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摘要

The ideal neuromuscular blocking agent (NMBA) is regarded as being a non-depolarizing equivalent of succinylcholine, having a rapid onset and short duration of action, with minimal side effects. In the absence of a single drug, the administration of an aminosteroid NMBA, such as rocuronium, followed by reversal using an acetylcholinesterase inhibitor, such as neostigmine, is commonly employed. A different and safer approach to rapidly reversing the action of the NMBA, by encapsulating it with a macrocyclic or acyclic host molecule, such as the cyclodextrin sugammadex or more recently, cucurbituril-type hosts such as cyclic cucurbit7uril and the acyclic glycoluril tetramer calabadion 1, is described.
机译:理想的神经肌肉阻滞剂 (NMBA) 被认为是琥珀胆碱的非去极化等效物,起效快,作用持续时间短,副作用最小。在没有单一药物的情况下,通常采用氨基类固醇NMBA(如罗库溴铵),然后使用乙酰胆碱酯酶抑制剂(如新斯的明)进行逆转。描述了一种不同的、更安全的方法来快速逆转NMBA的作用,方法是将其包裹在大环或无环宿主分子中,例如环糊精舒更葡糖,或最近的葫芦脲型宿主,例如环葫芦[7]脲和无环乙脲四聚体卡拉巴迪翁1。

著录项

  • 来源
    《Future medicinal chemistry》 |2013年第17期|2075-2089|共15页
  • 作者

    MacartneyD.H.;

  • 作者单位

    Department of Chemistry, Queen's University, Kingston, ON K7L 3N6, Canada;

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

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