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Transvascular and interstitial transport in rat hepatocellular carcinomas: Dynamic contrast-enhanced MRI assessment with low- and high-molecular weight agents.

机译:大鼠肝细胞癌的经血管和间质运输:低分子量和高分子量药物的动态对比增强MRI评估。

摘要

PURPOSE: To assess which MRI-derived kinetic parameters reflect decreased transvascular and interstitial transport when low- and high-molecular-weight agents are used in rat hepatocellular carcinomas. MATERIALS AND METHODS: Dynamic MRI after injection of a low-molecular-weight contrast agent of 0.56 kDa (Gd-DOTA, gadoterate) and two high-molecular-weight contrast agents of 6.47 kDa (P792, gadomelitol) and 52 kDa (P717, carboxymethyldextran Gd-DOTA) was performed in rats with chemically induced hepatocellular carcinomas. The data were analyzed with the Kety compartmental model, the extended Kety compartmental model in which it is assumed that the tissue voxels contain a vascular component, and the St Lawrence and Lee distributed-parameter model. RESULTS: The extravascular extracellular space accessible to the contrast agent v(e) and the extraction fraction E decreased with increasing molecular weight of the contrast agent. In contrast, the volume transfer constant Ktrans did not differ significantly when low- or high-molecular-weight agents were used. CONCLUSION: In this animal model the results suggest that the accessible extravascular extracellular space and the extraction fraction are more sensitive indicators of decreased transvascular and interstitial transport with high-molecular-weight agents than the volume transfer constant, which is a lumped representation of blood flow and permeability. J. Magn. Reson. Imaging 2008;28:906-914. (c) 2008 Wiley-Liss, Inc.
机译:目的:当在大鼠肝细胞癌中使用低分子量和高分子量药物时,评估哪些MRI衍生的动力学参数反映了减少的经血管和间质运输。材料与方法:注射0.56 kDa的低分子量造影剂(Gd-DOTA,g酸盐)和两种6.47 kDa的高分子量造影剂(P792,g糖醇)和52 kDa(P717,羧甲基葡聚糖Gd-DOTA)在患有化学诱导的肝细胞癌的大鼠中进行。使用Kety间隔模型,扩展的Kety间隔模型(其中假定组织体素包含血管成分)和St Lawrence and Lee分布参数模型对数据进行了分析。结果:随着造影剂分子量的增加,造影剂v(e)可进入的血管外空间和提取分数E减小。相反,当使用低分子量或高分子量试剂时,体积转移常数Ktrans没有显着差异。结论:在该动物模型中,结果表明,与体积转移常数相比,高分子量药物可减少的血管外细胞间隙和提取分数是减少血管和间质运输的更敏感指标,这是血流的集中表示。和渗透性。 J.Magn。雷森成像2008; 28:906-914。 (c)2008 Wiley-Liss,Inc.

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