未标记和放射性碘化罗丹明-123的体内研究

Manhar M. Vora, Mohammed Dhalla
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引用次数: 7

摘要

采用放射性碘化罗丹明-123 (Rh123)作为潜在的肿瘤显像剂,注射于实验性诱导肿瘤小鼠体内,观察其组织分布。在肿瘤中发现了一些放射性积累;大部分在注射后迅速从血液中清除。放射性碘化后的Rh123代谢为水溶性物质,通过尿液和粪便排出体外。另一方面,未标记的Rh123仅在肿瘤中少量积累。然而,人们发现它在心脏中显著积聚;注射后4小时血液中含量高达70倍。注射后24 h,未标记的Rh123积累量稳定增加;然而,它通过肾脏从血液中迅速清除。这种Rh123在心脏中选择性积累的发现可以用于合成11C-和18f标记的Rh123,用于心肌的PET研究。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
In vivo studies of unlabeled and radioiodinated rhodamine-123

Radioiodinated rhodamine-123 (Rh123), potential tumor imaging agent, was injected in mice bearing experimentally-induced tumors to investigate its tissue distribution. Some accumulation of radioactivity was found in tumors; most of it cleared rapidly from the blood after injection. Also, the radioiodinated Rh123 had metabolized to water-soluble species which was excreted in urine and feces.

Unlabeled Rh123, on the other hand, accumulated only marginally in the tumors. However, it was found to accumulate significantly in the heart; as much as seventy times the level in blood at 4 h post-injection. Accumulation of unlabeled Rh123 increased steadily even at 24 h post-injection; whereas, it cleared rapidly from the blood via the kidney.

This finding of selective accumulation of Rh123 in heart could be exploited in synthesizing 11C- and 18F-labeled Rh123 for use in PET studies of the myocardium.

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