Cheki Mohsen, Gali Hariprasad
Department of Radiologic Technology, Faculty of Paramedicine, Ahvaz Jundishapur University of Medical Sciences, Ahvaz, Iran.
Hell J Nucl Med. 2017 Sep-Dec;20(3):241-246. doi: 10.1967/s002449910609. Epub 2017 Nov 27.
In this study, we tried to estimate human absorbed dose of Ga-NODAGA-glycine as a new potential positron emission tomography (PET) renal agent based on the biodistribution data reported in healthy rats, and compare our estimation with the available absorbed dose data from technetium-99m-diethylenetriaminepentaacetic acid (Tc-DTPA).
The medical internal radiation dose (MIRD) formulation was applied to extrapolate from rats to human and to project the absorbed radiation dose for various organs in humans. S factor calculated by Monte-Carlo N-particle (MCNP) simulation and also this factor has been taken from the tables presented in MIRD pamphlet No.11. Hence, two radiation absorbed dose were calculated for organs.
Our dose prediction shows that an 185MBq injection of gallium-68-1,4,7-triazacyclononane-1-γ-glutamylglycine-4,7-diacetic acid (Ga-NODAGA-glycine) in humans might result in an estimated absorbed dose of 0.063mGy in the whole body when S factor calculated by MCNP simulation. The highest absorbed doses are observed in kidneys, lungs, spleen, liver, and red marrow with 3.510, 0.453, 0.335, 0.268, and 0.239mGy, respectively. In addition to, the estimated absorbed dose for total body after injection of 185MBq of Ga-NODAGA-glycine is 0.053mGy when S factor has been taken from MIRD pamphlet No.11. The highest absorbed doses are observed in kidneys, lungs, liver, spleen, and red marrow with 3.110, 0.438, 0.209, 0.203, and 0.203mGy, respectively. Comparison between human absorbed dose estimation for Ga-NODAGA-glycine and Tc-DTPA indicated that the absorbed dose of the most organs after injection of Tc-DTPA is higher than the amount after Ga-NODAGA-glycine.
The results showed that Ga-NODAGA-glycine delivers lower dose to the patients. Also due to its application in PET (which offers higher sensitivity and spatial resolution compared to planar or SPET), Ga-NODAGA-glycine would be a superior choice than Tc-DTPA for renography and impose less radiation doses to patients.
在本研究中,我们试图根据健康大鼠的生物分布数据,估算新型潜在正电子发射断层扫描(PET)肾显像剂镓-氮杂环三乙酸-甘氨酸(Ga-NODAGA-甘氨酸)的人体吸收剂量,并将我们的估算值与锝-99m-二乙三胺五乙酸(Tc-DTPA)的可用吸收剂量数据进行比较。
应用医学内照射剂量(MIRD)公式从大鼠外推至人体,预测人体各器官的吸收辐射剂量。通过蒙特卡罗N粒子(MCNP)模拟计算S因子,该因子也取自MIRD手册第11号中的表格。因此,计算了两个器官的辐射吸收剂量。
我们的剂量预测表明,在人体中注射185MBq的镓-68-1,4,7-三氮杂环壬烷-1-γ-谷氨酰甘氨酸-4,7-二乙酸(Ga-NODAGA-甘氨酸),当通过MCNP模拟计算S因子时,全身估计吸收剂量可能为0.063mGy。肾脏、肺、脾、肝和红骨髓的吸收剂量最高,分别为3.510、0.453、0.335、0.268和0.239mGy。此外,当S因子取自MIRD手册第11号时,注射185MBq Ga-NODAGA-甘氨酸后全身的估计吸收剂量为0.053mGy。肾脏、肺、肝、脾和红骨髓的吸收剂量最高,分别为3.110、0.438、0.209、0.203和0.203mGy。Ga-NODAGA-甘氨酸与Tc-DTPA人体吸收剂量估算值的比较表明,注射Tc-DTPA后大多数器官的吸收剂量高于注射Ga-NODAGA-甘氨酸后的剂量。
结果表明,Ga-NODAGA-甘氨酸给患者的剂量较低。此外,由于其在PET中的应用(与平面或单光子发射断层扫描相比,PET具有更高的灵敏度和空间分辨率),Ga-NODAGA-甘氨酸在肾造影方面将是比Tc-DTPA更好的选择,并且给患者施加的辐射剂量更小。