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Radioiodination and biological evaluation of Cimetidine as a new highly selective radiotracer for peptic ulcer disorder detection
Radiochimica Acta ( IF 1.4 ) Pub Date : 2020-11-05 , DOI: 10.1515/ract-2020-0046
Mahmoud H. Sanad 1 , Safaa B. Challan 1 , Fawzy A. Marzook 1 , Sayed M. Abd-Elhaliem 1 , Ebtisam A. Marzook 2
Affiliation  

One of the most famous techniques for stomach ulcer imaging is the nuclear imaging technique. We aim to focus on the synthesis of 125I-cimetidine (125I-cim) as an agent for peptic ulcer imaging. Cimetidine was labeled with Iodine-125 using a different oxidizing agent (Ch-T, NBS). All factors affecting the labeling yield were optimized. The radiochemical yield of 125I-cim was 98 ± 0.22% at optimum conditions. In vitro stability, in vivo biodistribution of 125I-cimetidine was studied in three groups: control group, pretreated group, and ulcer bearing group. In vivo biodistribution studies of 125I-cim revealed high uptake in the stomach ulcer, reaching about 75.4 ± 1.2% ID/g at 15 min post-injection, than pretreated groups compared to the control. The results showed the suitability of using 125I-cimetidine for stomach ulcer imaging.

中文翻译:

西咪替丁作为一种新型高选择性放射性示踪剂,用于消化性溃疡疾病的放射性碘标记和生物学评估

胃溃疡成像最著名的技术之一是核成像技术。我们的目标是专注于125 I-西咪替丁(125 I-cim)的合成,作为消化性溃疡成像的药物。使用另一种氧化剂(Ch-T,NBS)将碘美替丁(Imetine-125)标记为西咪替丁。所有影响标记产量的因素均已优化。在最佳条件下,125 I-cim的放射化学产率为98±0.22%。在体外稳定性方面,研究了三组125 I-西咪替丁的体内生物分布:对照组,预处理组和溃疡形成组。125体内生物分布研究与对照组相比,I-cim显示胃溃疡的摄取量高,在注射后15分钟时达到约75.4±1.2%ID / g。结果显示使用125 I-西咪替丁进行胃溃疡成像的适用性。
更新日期:2020-11-09
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