Biodistribution and dosimetry of free118Te, anin vivogenerator of the positron emitter118Sb for long-term positron emission tomography.

IF 3.1 3区 医学 Q2 ENGINEERING, BIOMEDICAL
Jaewoong Jang, Sotaro Miyao, Xindi Qiu, Toson Hamza, Yousuke Kanayama, Atsuko Nakanishi Ozeki, Yuki Mitsuya, Masako Kawabata, Izumi O Umeda, Toshimitsu Momose, Youichiro Wada, Hiromitsu Haba, Hiroyuki Takahashi, Nobuyoshi Akimitsu
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引用次数: 0

Abstract

Objective. Tellurium-118 (118Te;t1/2= 6.00 ± 0.02 d) can act as anin vivogenerator of the positron emitter antimony-118 (118Sb;t1/2= 3.6 ± 0.3 min), enabling positron emission tomography (PET) over a week or longer. This work assessed absorbed doses associated with free118Te to establish a dosimetric safety basis for118Te radiopharmaceuticals.Approach. Injection solutions of free118Te were prepared by alpha-particle irradiation of an enriched tin-116 target followed by radiochemical isolation.Ex vivobiodistribution in healthy female Slc:ICR mice was acquired at seven time points from 2 h to 29 d postinjection (n= 6 per time point). Time-integrated activity coefficients were computed from the biodistribution profiles and extrapolated to a human model using relative mass scaling. Absorbed dose coefficients (ADCs) were calculated following the Medical Internal Radiation Dose formalism with computational phantoms implemented in the dosimetry software OLINDA. Dosimetric contributions from118Te and its coproduced radioisotopic impurity119mTe (t1/2= 4.69 ± 0.04 d), along with their equilibrium daughters118Sb and119Sb, were individually assessed.Main results. The kidneys exhibited the highest ADC in both mouse (2666.0 mGy MBq-1) and human (2.639 mGy MBq-1) models. Bone received the second-highest ADC in the mouse model, 1855.5 mGy MBq-1. Antimony-118 dominated absorbed doses across all organs examined, accounting for more than 82% of ADCs in both models. Contributions from118Te,119mTe, and119Sb were minor by comparison.Significance. The kidneys and bone were identified as the primary dosimetric targets of free118Te, with its daughter118Sb being the principal dose contributor. The limited dosimetric impact from118Te provides justification for its use as anin vivogenerator of118Sb for long-term PET. The ADCs reported here offer a quantitative basis for assessing the dosimetric safety of118Te radiopharmaceuticals.

游离118te的生物分布和剂量学,正电子发射体118sb的一个活体发生器用于长期正电子发射断层扫描。
目标。碲-118 (118Te;t1/2= 6.00±0.02 d)可以作为正电子发射器锑-118 (118Sb;t1/2= 3.6±0.3 min)的活体发生器,使正电子发射断层扫描(PET)持续一周或更长时间。本工作评估与游离118te相关的吸收剂量,以建立118te放射性药物的剂量学安全基础。通过α粒子辐照富集的锡116靶,然后进行放射化学分离,制备了游离118te注射溶液。在注射后2 h至29 d的7个时间点(每个时间点n= 6)获得健康雌性Slc:ICR小鼠的体外分布。从生物分布曲线计算时间积分活度系数,并使用相对质量尺度外推到人类模型。吸收剂量系数(adc)按照医学内辐射剂量公式计算,并在剂量测定软件OLINDA中实现计算模型。分别评估了118te及其共同产生的放射性同位素杂质119mte (t1/2= 4.69±0.04 d)及其平衡子代118sb和119sb的剂量学贡献。主要的结果。小鼠模型(2666.0 mGy MBq-1)和人模型(2.639 mGy MBq-1)肾脏ADC均最高。骨在小鼠模型中获得第二高ADC,为1855.5 mGy MBq-1。锑-118在所有被检查器官的吸收剂量中占主导地位,在两种模型中占adc的82%以上。相比之下,118te、119mTe和119sb的贡献较小。肾脏和骨骼被确定为游离118te的主要剂量目标,其子元素118sb是主要剂量贡献者。118te有限的剂量学影响为其作为长期PET的118sb体内产生剂提供了理由。本文报道的adc为评估118te放射性药物的剂量安全性提供了定量基础。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Physics in medicine and biology
Physics in medicine and biology 医学-工程:生物医学
CiteScore
6.50
自引率
14.30%
发文量
409
审稿时长
2 months
期刊介绍: The development and application of theoretical, computational and experimental physics to medicine, physiology and biology. Topics covered are: therapy physics (including ionizing and non-ionizing radiation); biomedical imaging (e.g. x-ray, magnetic resonance, ultrasound, optical and nuclear imaging); image-guided interventions; image reconstruction and analysis (including kinetic modelling); artificial intelligence in biomedical physics and analysis; nanoparticles in imaging and therapy; radiobiology; radiation protection and patient dose monitoring; radiation dosimetry
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