The University of Tennessee Graduate School of Medicine, 1924 Alcoa Hwy., Knoxville, TN 37920, United States of America.
The University of Tennessee Graduate School of Medicine, 1924 Alcoa Hwy., Knoxville, TN 37920, United States of America; University of Tennessee Department of Mechanical, Aerospace, and Biomedical Engineering, United States of America.
Nucl Med Biol. 2019 Jul-Aug;74-75:41-48. doi: 10.1016/j.nucmedbio.2019.07.008. Epub 2019 Jul 22.
Fluorine-18 labeled radiopharmaceuticals undergo quality control testing for residual phase-transfer-catalyst content. The almost universally used quality-control test is a silica plate spot-test comparison of the radiopharmaceutical beside a 50-ppm standard. Once developed by staining, the radiopharmaceutical spot must be of equal or less intensity to pass the test. There is currently a need for a quantitative, inexpensive, and less subjective quality control method that allows the automatic incorporation of the acquired measurement directly into electronic batch reports.
In the developed method, a resazurin test solution is mixed with an aliquot of the radiopharmaceutical analyte along with dichloromethane (DCM). The mixture is vortexed. The potassium resazurin-phase transfer catalyst complex solubilizes into the DCM imparting a blue color. The organic layer is then removed for analysis. Three measurement methods were utilized: visual colorimetry against pre-prepared standards, spectrophotometric measurement of transmittance, and electrical conductance. A simple prototype spectrophotometer and an electrical test cell were constructed to acquire data. Sodium Resazurin dye was found to be a suitable test chromophore for residual phase transfer catalyst analysis of aqueous solutions. Quantitative spectrophotometric measurements are possible in the 0-100-ppm range (18-crown-6) and 0-150-ppm range (Kryptofix® or tetrabutylammonium). Electrical resistance measurements of the phase transfer-catalyst resazurin complex in DCM are also a viable method, allowing quantitative phase transfer catalyst measurements in the 0-100-ppm range.
The methodologies developed are more quantitative alternatives to the current spot-test method. The spectrophotometric method was determined to be the most accurate method.
氟-18 标记放射性药物需要进行残留相转移催化剂含量的质量控制测试。目前几乎普遍使用的质量控制测试是在 50ppm 标准旁边用硅胶板斑点测试来比较放射性药物。一旦通过染色进行开发,放射性药物斑点的强度必须相等或更小才能通过测试。目前需要一种定量、廉价和较少主观的质量控制方法,允许将获得的测量值直接自动纳入电子批报告中。
在开发的方法中,将 Resazurin 测试溶液与放射性药物分析物的等分试样以及二氯甲烷 (DCM) 混合。将混合物涡旋。钾 Resazurin-相转移催化剂络合物溶解在 DCM 中,赋予蓝色。然后去除有机层进行分析。使用了三种测量方法:与预制标准进行目视比色、透光率的分光光度测量和电导率。构建了一个简单的原型分光光度计和一个电测试池来获取数据。发现 Resazurin 染料是用于水相溶液中残留相转移催化剂分析的合适测试生色团。在 0-100-ppm 范围(18-冠-6)和 0-150-ppm 范围内可以进行定量分光光度测量(Kryptofix®或四丁基铵)。DCM 中相转移催化剂 Resazurin 络合物的电阻测量也是一种可行的方法,允许在 0-100-ppm 范围内进行定量相转移催化剂测量。
所开发的方法是对当前斑点测试方法的更定量替代方法。分光光度法被确定为最准确的方法。