Grupo de Protecção e Segurança Radiológica, Centro de Ciências e Tecnologias Nucleares (C2TN), CTN/IST, Pólo de Loures. Estrada Nacional 10 (km 139,7), 2695-066 Bobadela LRS, Portugal.
Grupo de Protecção e Segurança Radiológica, Centro de Ciências e Tecnologias Nucleares (C2TN), CTN/IST, Pólo de Loures. Estrada Nacional 10 (km 139,7), 2695-066 Bobadela LRS, Portugal; Departamento de Física, Faculdade de Ciências e Tecnologias da Universidade Nova de Lisboa, Quinta da Torre, Campus Universitário, 2829-516 Caparica, Portugal.
Phys Med. 2018 Aug;52:9-17. doi: 10.1016/j.ejmp.2018.06.010. Epub 2018 Jun 15.
Biokinetic data from the administration of radiopharmaceuticals is essential in nuclear medicine dosimetry. It has particular significance in children, as their metabolism is very different from adults. Biokinetic models for paediatric patients could therefore need to be adapted to better reflect their absorption, retention and excretion functions, when compared to adults. Obtaining quality in vivo infant or paediatric biokinetic data is then essential to improve the available reference models, which in turn can lead to the optimization of paediatric procedures and protocols in clinical practice. This study analyses the biokinetic behaviour of Tc-dimercaptosuccinic acid (DMSA), in 8 infants aged 4 months to 2 years old, through an imaging study using a gamma camera, and compares the obtained values with those obtained with the reference ICRP biokinetic model. The in vivo data was treated using an adapted methodology from the MIRD 16 pamphlet. Activity curves for the liver, the kidney and the whole body, were built, and new effective absorption, retention and excretion half-lives were estimated, and compared with the reference biokinetic parameters of ICRP 128. The obtained residence time in the kidneys of 2.56 h, has a deviation of 30.8% to the ICRP 128 value of 3.70 h. The obtained maximum uptake in the kidneys was of 0.22/A, which compares to the value of 0.31/A for ICRP. The obtained biokinetic parameters were used to estimate the absorbed dose. The obtained dose values are smaller than the reference ICRP 128 ones by 32.1% in the kidneys, and 18.4% in the liver.
放射性药物给药的生物动力学数据是核医学剂量学的基础。对于儿童来说,这些数据尤为重要,因为他们的新陈代谢与成年人有很大的不同。因此,与成年人相比,儿科患者的生物动力学模型可能需要进行调整,以更好地反映他们的吸收、保留和排泄功能。为了改善现有的参考模型,从而优化儿科临床实践中的程序和方案,获得高质量的婴儿或儿科体内生物动力学数据是至关重要的。本研究通过伽马相机成像研究分析了 8 名 4 个月至 2 岁婴儿的 Tc-二巯丁二酸(DMSA)的生物动力学行为,并将获得的值与 ICRP 参考生物动力学模型进行了比较。使用 MIRD 16 小册子中的一种适应性方法对体内数据进行了处理。构建了肝脏、肾脏和全身的活性曲线,并估计了新的有效吸收、保留和排泄半衰期,并与 ICRP 128 的参考生物动力学参数进行了比较。获得的肾脏停留时间为 2.56 小时,与 ICRP 128 的 3.70 小时值偏差为 30.8%。获得的肾脏最大摄取量为 0.22/A,而 ICRP 的值为 0.31/A。使用获得的生物动力学参数来估计吸收剂量。获得的剂量值在肾脏中比 ICRP 128 的参考值小 32.1%,在肝脏中则小 18.4%。