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关于99mTc(V)-二巯基丁二酸分布的生物动力学和剂量学研究。

Biokinetics and dosimetric studies about 99mTc(V)-DMSA distribution.

作者信息

Correia M B L, Magnata S S L P, Silva I M S, Catanho M T J A, Lima F F

机构信息

Nuclear Energy Department, Universidade Federal de Pernambuco, Recife, PE, Brazil.

出版信息

Cell Mol Biol (Noisy-le-grand). 2010 May 10;56(2):1-5.

Abstract

Research for radiodiagnostic agents should considerate biological critical parameters which will give own contribution on the absorbed dose. The dimercaptosuccinic acid (DMSA) labeled with (99m)Tc(V) is a radiopharmaceutical which has well established role in medullar thyroid carcinoma and has been proposed in evaluation of bone metastasis. This work studied the biokinetics and dosimetry of (99m)Tc(V)-DMSA by animal model. The (99m)Tc(V)-DMSA was prepared from a (III)DMSA kit alkalized. Mice (n=5) received (99m)Tc(V)DMSA i.v., they were sacrificed (30 min, 1h, 5h and 12h), the organs excised and the activities measured by a gamma counter. The results were evaluated based on %activity/g and the absorbed dose was estimated (MIRDOSE 3.0 program) by extrapolation of data from animal to human scale. The results showed the majority of organs reached the top uptake at 30 min, the greatest kidney uptake was (4.81 +/- 1.38)% activity/g, while the bone presented its highest uptake at 1h (5.49+/- 0.47)% activity/g, after 1h all the organs had activity exponential decrease. The biokinetic profile of (99m)Tc(V)-DMSA was well established, allowing quantifying of residence time, and the radiation dose estimates were made for this agent. About the absorbed dose, the preliminary results showed higher value to bone, being the soft tissue dose relatively low.

摘要

放射性诊断剂的研究应考虑对吸收剂量有自身贡献的生物学关键参数。用(99m)Tc(V)标记的二巯基丁二酸(DMSA)是一种放射性药物,在甲状腺髓样癌中具有明确的作用,并已被用于骨转移的评估。这项工作通过动物模型研究了(99m)Tc(V)-DMSA的生物动力学和剂量学。(99m)Tc(V)-DMSA由碱化的(III)DMSA试剂盒制备。小鼠(n = 5)静脉注射(99m)Tc(V)DMSA,在(30分钟、1小时、5小时和12小时)处死,切除器官并用γ计数器测量活性。根据每克活性百分比评估结果,并通过将动物数据外推至人体尺度来估计吸收剂量(MIRDOSE 3.0程序)。结果显示,大多数器官在30分钟时达到最高摄取量,肾脏的最大摄取量为(4.81±1.38)%活性/克,而骨骼在1小时时呈现最高摄取量(5.49±0.47)%活性/克,1小时后所有器官的活性呈指数下降。(99m)Tc(V)-DMSA的生物动力学特征已明确,可对停留时间进行量化,并对该药物进行了辐射剂量估计。关于吸收剂量,初步结果显示骨骼的吸收剂量较高,而软组织剂量相对较低。

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