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99mTc-labeling studies of a modified metronidazole and its biodistribution in tumor bearing animal models.

机译:修饰甲硝唑的99mTc标记研究及其在荷瘤动物模型中的生物分布。

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摘要

A cysteine-based bifunctional chelating agent viz. N-(2'-hydroxybenzyl)-cysteine with a free carboxylic acid group (CAA) was synthesized. Bearing in mind the affinity of localization of nitroimidazoles in hypoxic tissues, this bifunctional chelating agent was coupled to metronidazole (MNZ). The (99m)Tc labeling studies of the novel agent (MNZCAA) thus obtained, was carried out and the radiolabeled product was subsequently purified. The complexation yield under optimized condition was approximately 85%. Biodistribution studies carried out in Swiss mice bearing 'barcl-95' tumors showed selective accumulation of the injected activity in the tumor (1.70%/g at 30 min p.i.) with renal as well as hepatobiliary clearance. High tumor/muscle ratio (14.7 at 3 h post-injection) of the novel agent indicates considerable promise towards further evaluation.
机译:基于半胱氨​​酸的双功能螯合剂。合成具有游离羧酸基团(CAA)的N-(2'-羟基苄基)-半胱氨酸。考虑到硝基咪唑在低氧组织中的定位亲和力,该双功能螯合剂与甲硝唑(MNZ)偶联。进行了如此获得的新药(MNZCAA)的(99m)Tc标记研究,随后纯化了放射性标记的产物。在优化条件下的络合产率约为85%。在患有“ barcl-95”肿瘤的瑞士小鼠中进行的生物分布研究表明,注射的活性在肾脏和肝胆清除率中选择性积累(在30分钟p.i时为1.70%/ g)。该新型药物的高肿瘤/肌肉比率(注射后3 h时为14.7)表明有希望进一步评估。

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