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电子自旋共振光谱在毒理学中的应用。

Application of ESR spectroscopy in toxicology.

作者信息

McCay P B

出版信息

Arch Toxicol. 1987;60(1-3):133-7. doi: 10.1007/BF00296966.

Abstract

Spin trapping in vivo was first achieved in the author's laboratory and is shown to be a feasible method for demonstrating that highly reactive free radical intermediates are generated in the tissues of intact animals as a result of the exposure to certain toxic compounds and to ionizing radiation. The method is based on the property of spin trapping agents (nitrones) to react readily with reactive free radicals to produce stable radical adducts at the site of their origin in target organs. The radical adducts can then be detected by electron spin resonance spectroscopy to determine the intensity of radical production (i.e., number of radicals which were trapped), and, in most cases, identify the nature of the radical that was produced. The type of spin trapping agent employed determines the type of radicals which can be trapped and, at this stage of development of the technique, the number of useful in vivo trapping agents is rather limited.

摘要

体内自旋捕获技术最初是在作者的实验室中实现的,并且已证明它是一种可行的方法,可用于证明完整动物组织中由于接触某些有毒化合物和电离辐射而产生高反应性自由基中间体。该方法基于自旋捕获剂(硝酮)的特性,即它们能与反应性自由基迅速反应,在靶器官中自由基产生的部位生成稳定的自由基加合物。然后可以通过电子自旋共振光谱法检测自由基加合物,以确定自由基产生的强度(即被捕获的自由基数量),并且在大多数情况下,确定所产生自由基的性质。所使用的自旋捕获剂的类型决定了可以捕获的自由基的类型,并且在该技术的现阶段,体内可用的捕获剂数量相当有限。

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