用含有18f残留标记的正电子发射断层扫描定量评估脂蛋白代谢

Alan Daugherty , Michael R. Kilbourn , Carmen S. Dence , Burton E. Sobel , Suzanne R. Thorpe
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引用次数: 3

摘要

蛋白质的残留标记被设计成在载体蛋白摄取和降解后仍被困在细胞内。在目前的工作中,我们报道了一种新型残留标记n -乳酸- s -([18F]氟苯酰基)-半胱胺([18F]LCSH)的合成,并通过正电子发射断层扫描(PET)用于定量体内组织中低密度脂蛋白的积累。用[18F]LCSH标记的脂蛋白或其他快速分解代谢的蛋白药物的降解产物在组织中的保留减少了示踪剂渗漏到血浆室。因此,残差标记为提高信噪比提供了一个有价值的工具,即使在相对较短的PET研究间隔期间也是如此。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Quantitative assessment of lipoprotein metabolism by positron emission tomography with an 18F-containing residualizing label

Residualizing labels for proteins are designed to remain entrapped within cells following uptake and degradation of the carrier protein. In the present work we report the synthesis of a novel residualizing label, N-lactitol-S-([18F]fluorophenacyl)-cysteamine ([18F]LCSH, and its use for quantifying the accumulation of low density lipoprotein in tissues in vivo by positron emission tomography (PET). The retention of degradation products in tissues from lipoprotein or from other rapidly catabolized protein pharmaceuticals tagged with [18F]LCSH reduces leakage of tracer into the plasma compartment. Thus, residualizing labels provide a valuable tool for enhancing signal-to-noise ratios, even during the relatively short interval of PET studies.

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