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Chinda Lerthirunwong , Kenneth T. Cheng , William B. Hladik III
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引用次数: 3

摘要

传统上,当制备99mTc标记的放射性药物时,将[99mTc]高技术酸盐添加到小瓶试剂盒的整个内容物中,然后从小瓶中取出患者剂量。由于两个原因,这种复合技术可能会造成潜在的浪费:(1)一旦用99mTc重组,大多数试剂盒的保质期相对较短,因此在到期前可能不会使用全部内容;(2)由于许多医院需要保存放射性,因此在试剂盒中添加足够的[99mTc]高技术酸盐,以便仅检索1 - 2个患者剂量,即使试剂盒中存在足够的化学物质(配体,还原剂等),以提供多达5-10个剂量。因此,需要一种优化有效使用试剂盒的方法。本研究的目的是确定单位剂量非放射性试剂试剂盒的可行性,并将这些冷单位剂量(CUDs)储存起来,以便最终用99mTc进行标记。为了评估这一概念,从甲氧膦酸钠(MDP)和戊酸酯(DTPA)的试剂盒中制备了单位剂量。本研究研究的具体变量是储存时间、储存温度和重构体积(稀释度)对单位剂量的影响。这些效应是通过测量单位剂量的放射化学和生物分布特性来监测的,然后用[99mTc]高技术酸盐进行最终重构。采用即时薄层色谱法(ITLC)测定其标记效率,并研究其在小鼠体内的生物分布规律。结果表明,MDP-和DTPA-CUDs在- 18°C下保存30天后仍能保持良好的放射化学纯度和生物分布。另一方面,单位剂量的MDP和DTPA在25℃下贮存的放射化学纯度迅速下降。第30天的平均放射化学纯度低至0.58-19.4%。观察到生物分布的改变与标记效率的降低一致。低稀释度(3ml)的CUDs比高稀释度(10ml)的CUDs更稳定。然而,重构体积对cud的影响远不如温度对cud的影响显著。最后,单位剂量非放射性试剂包的概念似乎为制备不经常和紧急的放射性药物剂量提供了一种有效和节省成本的方法。研究还表明,这些单位剂量的储存温度对程序的成功至关重要。如果在适当的温度下储存,重构体积对cd的稳定性影响最小。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
A study of the concept of non-radioactive unit-dosed reagent kits [cold unit doses (CUDs)] as an efficient and cost-saving method for 99mTc radiopharmaceutical preparation

Traditionally, when preparing 99mTc-labeled radiopharmaceuticals, [99mTc]pertechnetate is added to the entire contents of a vial of reagent kit, and patient doses are subsequently withdrawn from the vial. This technique of compounding can be potentially wasteful for two reasons: (1) once reconstituted with 99mTc, most reagent kits have a relatively short shelf-life, and thus the entire contents may not be used before expiration and (2) due to a need to conserve radioactivity in many hospitals, enough [99mTc]pertechnetate is added to the reagent kit in order to retrieve only 1–2 patient doses, even though adequate chemicals (ligand, reducing agent, etc.) are present in the reagent kit to supply as many as 5–10 doses. Hence, a method for optimizing the efficient use of reagent kits would be desirable. The purpose of this study was to determine the feasibility of unit-dosing non-radioactive reagent kits and storing these cold unit doses (CUDs) for eventual labeling with 99mTc. To evaluate this concept, unit doses were prepared from reagent kits of medronate (MDP) and pentetate (DTPA). The specific variables studied in this research were the effects of storage time, storage temperature and reconstitution volume (dilution) on the unit doses. These effects were monitored by measuring the radiochemical and biodistribution properties of the unit doses following their final reconstitution with [99mTc]pertechnetate. The labeling efficiency was determined using instant thin layer chromatography (ITLC), and the biodistribution patterns of these radiolabeled CUDs were studied in mice. The results showed that MDP- and DTPA-CUDs stored at −18 °C retained the properties which resulted in acceptable radiochemical purity and biodistribution in mice for as long as 30 days. On the other hand, the radiochemical purity of MDP and DTPA unit doses stored at 25 °C deteriorated rapidly. Mean radiochemical purities as low as 0.58–19.4% were observed on day 30. Altered biodistributions were observed in a manner consistent with the decreased labeling efficiencies. The CUDs of lower dilution (3 mL) appeared to be more stable than the CUDs of higher dilution (10 mL). However, the effect of reconstitution volume was much less significant than the temperature effect on the CUDs. In conclusion, the concept of unit-dosing non-radioactive reagent kits appears to provide an efficient and cost-saving method for preparing infrequent and emergency radiopharmaceutical doses. The study also showed that the storage temperature of these unit doses is critical to the success of the procedure. The volume of reconstitution has a minimal impact on the stability of CUDs if stored at the appropriate temperature.

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