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Preparation and biodistribution of novel ~(99m)Tc(CO)_3-CNR complexes for myocardial imaging

机译:新型〜(99m)Tc(CO)_3-CNR心肌显像复合物的制备及生物分布

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摘要

We evaluated lipophilicity and biodistribution of a series of ~(99m)Tc(CO)_3-ether isonitrile complexes to determine whether different lipophilicity and structure of isonitrile ligands would improve the imaging properties of the radiopharmaceutical for the heart. Novel ~(99m)Tc(CO)_3-MIBI analogs were prepared and analyzed by radio-HPLC, and their lipophilicity was determined. These new complexes could be bi- or tri-substituted in specified pH conditions like ~(99m)Tc(CO)_3-MIBI. These new complexes exhibited low liver, lungs and blood uptake compared with [~(99m)Tc(CO)_3(MIBI)_3]~+ though their heart uptake was not so high. Among these complexes, [~(99m)Tc(CO)_3(EPI)_2(OH_2)]~+ showed higher target to non-target ratios at 5 and 30 min post-injection than that of [~(99m)Tc(CO)_3(MIBI)_3]~+.
机译:我们评估了一系列〜(99m)Tc(CO)_3-醚异腈复合物的亲脂性和生物分布,以确定不同的亲脂性和异腈配体的结构是否会改善心脏放射性药物的成像性能。制备了新型〜(99m)Tc(CO)_3-MIBI类似物并通过放射-HPLC分析,并确定了它们的亲脂性。这些新的复合物可以在特定的pH条件(例如〜(99m)Tc(CO)_3-MIBI)下被双或三取代。与[〜(99m)Tc(CO)_3(MIBI)_3]〜+相比,这些新复合物的肝脏,肺和血液摄取量低,尽管它们的心脏摄取量并不高。在这些配合物中,[〜(99m)Tc(CO)_3(EPI)_2(OH_2)]〜+在注射后5和30分钟时显示出比[〜(99m)Tc( CO)_3(MIBI)_3]〜+。

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