Production of non-standard PET radionuclides and the application of radiopharmaceuticals labeled with these nuclides.

M J Welch, R Laforest, J S Lewis
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引用次数: 17

Abstract

The field of positron emission tomography (PET) has expanded dramatically over recent years. In spite of this expansion the large majority of clinical studies are carried out utilizing one radiopharmaceutical-2-fluoro-2-deoxyglucose. Many research groups are developing novel radiopharmaceuticals. A major emphasis is on other agents labeled with 18F. Several other positron emitting radionuclides can be prepared in high yields in small biomedical cyclotrons. Some of these have half-lives that make delivery significantly easier than the delivery of 18F compounds. These radionuclides include: 64Cu (half life 12.7 h), 76Br (half life 16.2 h), 86Y (half life 14.74 h) and 124I (half life 4.2 days). The method of production of these and other 'non-standard' PET radionuclides will be discussed and the method of labeling radiopharmaceuticals with these radionuclides described. Several of these radiopharmaceuticals have been studied in animal models as well and a limited number translated to the human situation.

非标准PET放射性核素的生产和用这些核素标记的放射性药物的应用。
近年来,正电子发射断层扫描(PET)的研究领域得到了极大的发展。尽管有这种扩大,但绝大多数临床研究是利用一种放射性药物-2-氟-2-脱氧葡萄糖进行的。许多研究小组正在开发新的放射性药物。重点是其他标有18F的药剂。其他几种正电子发射放射性核素可以在小型生物医学回旋加速器中以高产量制备。其中一些化合物的半衰期比18F化合物的半衰期容易得多。这些放射性核素包括:64Cu(半衰期12.7小时)、76Br(半衰期16.2小时)、86Y(半衰期14.74小时)和124I(半衰期4.2天)。将讨论这些和其他“非标准”PET放射性核素的生产方法,并描述用这些放射性核素标记放射性药物的方法。其中一些放射性药物也在动物模型中进行了研究,并将有限数量的放射性药物应用于人类。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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