{"title":"Biodistribution and dosimetry of free<sup>118</sup>Te, an<i>in vivo</i>generator of the positron emitter<sup>118</sup>Sb for long-term positron emission tomography.","authors":"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","doi":"10.1088/1361-6560/aeb089","DOIUrl":null,"url":null,"abstract":"<p><p><i>Objective</i>. Tellurium-118 (<sup>118</sup>Te;<i>t</i><sub>1/2</sub>= 6.00 ± 0.02 d) can act as an<i>in vivo</i>generator of the positron emitter antimony-118 (<sup>118</sup>Sb;<i>t</i><sub>1/2</sub>= 3.6 ± 0.3 min), enabling positron emission tomography (PET) over a week or longer. This work assessed absorbed doses associated with free<sup>118</sup>Te to establish a dosimetric safety basis for<sup>118</sup>Te radiopharmaceuticals.<i>Approach</i>. Injection solutions of free<sup>118</sup>Te were prepared by alpha-particle irradiation of an enriched tin-116 target followed by radiochemical isolation.<i>Ex vivo</i>biodistribution in healthy female Slc:ICR mice was acquired at seven time points from 2 h to 29 d postinjection (<i>n</i>= 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 from<sup>118</sup>Te and its coproduced radioisotopic impurity<sup>119m</sup>Te (<i>t</i><sub>1/2</sub>= 4.69 ± 0.04 d), along with their equilibrium daughters<sup>118</sup>Sb and<sup>119</sup>Sb, were individually assessed.<i>Main results</i>. The kidneys exhibited the highest ADC in both mouse (2666.0 mGy MBq<sup>-1</sup>) and human (2.639 mGy MBq<sup>-1</sup>) models. Bone received the second-highest ADC in the mouse model, 1855.5 mGy MBq<sup>-1</sup>. Antimony-118 dominated absorbed doses across all organs examined, accounting for more than 82% of ADCs in both models. Contributions from<sup>118</sup>Te,<sup>119m</sup>Te, and<sup>119</sup>Sb were minor by comparison.<i>Significance</i>. The kidneys and bone were identified as the primary dosimetric targets of free<sup>118</sup>Te, with its daughter<sup>118</sup>Sb being the principal dose contributor. The limited dosimetric impact from<sup>118</sup>Te provides justification for its use as an<i>in vivo</i>generator of<sup>118</sup>Sb for long-term PET. The ADCs reported here offer a quantitative basis for assessing the dosimetric safety of<sup>118</sup>Te radiopharmaceuticals.</p>","PeriodicalId":20185,"journal":{"name":"Physics in medicine and biology","volume":" ","pages":""},"PeriodicalIF":3.1000,"publicationDate":"2026-10-05","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Physics in medicine and biology","FirstCategoryId":"5","ListUrlMain":"https://doi.org/10.1088/1361-6560/aeb089","RegionNum":3,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"ENGINEERING, BIOMEDICAL","Score":null,"Total":0}
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.
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