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Gamma-ray spectrometric measurement of radionuclide purity of radiopharmaceuticals contained in bottle samples

机译:瓶样品中所含放射性药物的放射性核素的伽马射线能谱测量

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摘要

The radionuclide purity of a radiopharmaceutical product is usually measured by gamma-rayudspectrometry with various measurement geometries. The importance of this test is that the radionuclide impurities, if present, result in an increase in the radiation dose to the patient without contributing to diagnostic information and in some cases may also interfere with the marking molecules and affect the proper conduct of diagnostic examination. In this work,udgamma-ray spectrometry is used to determine the amounts of impurities by adopting as measurement geometry the same bottle containing eluted or prepared radiopharmaceuticals. Inudaddition to high-purity germanium semiconductor detectors, the usefulness of NaI(Tl) and LaBr3(Ce) scintillators in routine operation is also examined. For the latter detectors, an evaluation of the minimum detectable activity was carried out and compared with the activity limits established by the regulation rules. The main cases considered are related to the first elution of 99Mo-99mTc generators and samples of 18F-FDG (fluoro-deoxy-glucose) to be used for positron emission tomography diagnostics.
机译:放射性药物产品的放射性核素纯度通常通过具有各种测量几何形状的伽马射线超谱法进行测量。该测试的重要性在于,如果存在放射性核素杂质,则会增加对患者的辐射剂量,而无助于诊断信息,并且在某些情况下还可能干扰标记分子并影响诊断检查的正确进行。在这项工作中,乌德伽玛射线光谱法通过采用装有洗脱或制备的放射性药物的同一瓶作为测量几何形状,来确定杂质含量。除高纯度锗半导体探测器外,还检查了NaI(Tl)和LaBr3(Ce)闪烁体在常规操作中的实用性。对于后一种检测器,对最低可检测活性进行了评估,并将其与法规规定的活性极限进行了比较。所考虑的主要案例与99Mo-99mTc发生器的首次洗脱和用于正电子发射断层扫描诊断的18F-FDG(氟脱氧葡萄糖)样品有关。

著录项

  • 作者

    Tomarchio E;

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  • 年度 2012
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  • 原文格式 PDF
  • 正文语种 eng
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