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作为潜在心肌显像剂的125I标记普拉洛尔二价类似物的合成与生物分布

Synthesis and biodistribution of 125I labeled bivalent analogs of practolol as potential myocardial imaging agents.

作者信息

Kizuka H, Hanson R N

出版信息

Int J Rad Appl Instrum B. 1986;13(5):551-5. doi: 10.1016/0883-2897(86)90137-6.

Abstract

Iodinated bivalent ligands 3 and 4 and a monovalent ligand 5 were prepared from the cardioselective beta-antagonist, practolol. 125I-labeled 3, 4 and 5 were prepared by solid phase isotopic exchange reaction with carrier-free Na125I and examined in rats as potential receptor-site-directed myocardial imaging agents. Biodistribution of these agents in rats indicated that 125I-3 and 125I-4 were localized in the heart similarly to 125I-5 and the [125I]iodobenzoyl (6) that was previously reported. Localization of 125I-3 and 125I-4, was more persistent in the heart than that of 125I-monovalent ligands 5 and 6. Heart-to-blood ratios of 125I-3 and 125I-4 were significantly lower than those of 125I-5 and 125I-6, due mainly to slow blood clearance rates of 125I-3 and 125I-4.

摘要

碘化二价配体3和4以及一价配体5由心脏选择性β受体拮抗剂心得宁制备而成。用无载体的Na125I通过固相同位素交换反应制备了125I标记的3、4和5,并在大鼠体内作为潜在的受体位点导向心肌显像剂进行了研究。这些药剂在大鼠体内的生物分布表明,125I-3和125I-4在心脏中的定位与125I-5以及先前报道的[125I]碘苯甲酰(6)相似。125I-3和125I-4在心脏中的定位比125I一价配体5和6更持久。125I-3和125I-4的心脏与血液的比率显著低于125I-5和125I-6,这主要是由于125I-3和125I-4的血液清除率较慢。

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