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新型含 5-硝基咪唑二硫代氨基甲酸盐(99mTc)配合物的合成及生物学特性研究作为靶向缺氧的潜在药物。

Synthesis and biological characterisation of novel dithiocarbamate containing 5-nitroimidazole (99m)Tc-complexes as potential agents for targeting hypoxia.

机构信息

Cátedra de Radioquímica, Facultad de Química, Gral Flores 2124, Universidad de la República, 11800 Montevideo, Uruguay.

出版信息

Bioorg Med Chem Lett. 2011 Jan 1;21(1):394-7. doi: 10.1016/j.bmcl.2010.10.130. Epub 2010 Oct 30.

Abstract

With the aim to develop new potential (99m)Tc-radiopharmaceuticals for imaging hypoxia based on the formation of Tc-nitrido complexes, two novel dithiocarbamate containing metronidazole derivatives (L1 and L2) have been prepared and characterised. The synthesis of L1 and L2 was achieved in excellent yield and high purity. Labelling with (99m)Tc was successfully performed using a low ligand concentration (approximately 2-3mg) and the desired products were obtained with high radiochemical purity (>90%). Lipophilicity, plasma protein binding, and biodistribution in normal- and tumour-bearing-CD1 mice studies were performed to asses the potentiality for nuclear medicine oncology. According to the physicochemical and biological behaviour both in healthy animals and in animals bearing solid tumours complex dtcTc1 could be considered as a starting point for the development of new radiopharmaceuticals for imaging hypoxia.

摘要

为了开发基于 Tc-亚硝络合物形成的新型用于缺氧成像的 (99m)Tc 放射性药物,我们制备并表征了两种新型含二硫代氨基甲酸盐的甲硝唑衍生物(L1 和 L2)。L1 和 L2 的合成产率高、纯度高。使用低配体浓度(约 2-3mg)成功地进行了 (99m)Tc 标记,获得了高放射化学纯度(>90%)的所需产物。通过在正常和荷瘤-CD1 小鼠中进行亲脂性、血浆蛋白结合和生物分布研究,评估了其在核医学肿瘤学中的潜力。根据健康动物和荷瘤动物的理化和生物学行为,dtcTc1 配合物可被视为开发用于缺氧成像的新型放射性药物的起点。

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