首页> 外文期刊>Journal of Radioanalytical and Nuclear Chemistry >Labeling of new formulation of tin–sucralfate freeze-dried kit with technetium-99m and its biological evaluation
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Labeling of new formulation of tin–sucralfate freeze-dried kit with technetium-99m and its biological evaluation

机译:m 99m标记硫糖铝锡冻干试剂盒新配方及其生物学评价

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摘要

The present investigation deals with a simple preparation of new formulation of tin–sucralfate freeze-dried kit (F.D.K.), to be directly labeled with 99mTc at optimal pH value of 7.0. The lyophilized form containing 100 mg sucralfate and 11.3 mg dihydrated stannous chloride. Other optimal pH values of the preparation were found to be from 4.0 to 11.0. The range of sucralfate amount studied (50–500 mg) not affected the radiochemical purity of the labeled complex. The radiochemical purity and the stability of the labeled preparation that assessed by filtration were more than 95%. 99mTc sucralfate was radiochemical stable up to a specific activity of 1,000 mCi per gram which was more stable than earlier published value (700 mCi per gram) without any radiolytic decomposition. The biological behavior of 99mTc-pertechnetate was evaluated in two groups of animals, the first group (neither fasted nor ulcerated) and the second group (fasted and ulcerated mice). The data of organ distribution of 99mTc–sucralfate in ulcerated fasted mice showed that more than 99% of the administered dose was accumulated in the stomach (87.92%) and intestine (11.43%). The radioanalytical results together with the in vivo-biological behavior of the labeled preparation demonstrate it’s stability, efficacy and usefulness in medical applications for the detection of gastrointestinal ulcers.
机译:本研究涉及一种新的硫糖铝锡冻干试剂盒(F.D.K.)新配方的简单制备方法,该试剂盒可在最佳pH值为7.0时直接用99mTc标记。该冻干形式含有100mg硫糖铝酸盐和11.3mg二水合氯化亚锡。发现该制剂的其他最佳pH值为4.0至11.0。研究的硫糖铝含量范围(50-500 mg)不影响标记复合物的放射化学纯度。通过过滤评估的标记制剂的放射化学纯度和稳定性大于95%。 99mTc硫糖铝酸盐在达到1000 mCi / g的比活度时是放射化学稳定的,比没有任何辐射分解的早期公布值(700 mCi / g)更稳定。在两组动物中评估了99mTc-高tech酸酯的生物学行为,第一组(既不禁食也不溃疡)和第二组(禁食和溃疡小鼠)。溃疡禁食小鼠中99mTc-硫糖铝的器官分布数据表明,超过99%的给药剂量累积在胃(87.92%)和肠(11.43%)中。放射分析的结果以及标记制剂的体内生物学行为表明,该制剂在医疗应用中用于检测胃肠道溃疡的稳定性,功效和有用性。

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