Radiosynthesis of clinical doses of 68 Ga-DOTATATE (GalioMedix™) and validation of organic-matrix-based 68 Ge/ 68 Ga generators

التفاصيل البيبلوغرافية
العنوان: Radiosynthesis of clinical doses of 68 Ga-DOTATATE (GalioMedix™) and validation of organic-matrix-based 68 Ge/ 68 Ga generators
المؤلفون: Izabela Tworowska, Ebrahim S. Delpassand, Sanjay Thamake, Konstantin Zhernosekov, Sebastian Marx, David Ranganathan, Alireza Mojtahedi, Michael K. Schultz
المصدر: Nuclear Medicine and Biology. 43:19-26
بيانات النشر: Elsevier BV, 2016.
سنة النشر: 2016
مصطلحات موضوعية: Cancer Research, Light nucleus, Hydrogen compounds, business.industry, Chemistry, Radiosynthesis, Radiochemistry, Clinical grade, Inorganic acids, Patient care, 030218 nuclear medicine & medical imaging, 03 medical and health sciences, 0302 clinical medicine, Isotopes of gallium, 030220 oncology & carcinogenesis, Molecular Medicine, Radiology, Nuclear Medicine and imaging, Organic matrix, Nuclear medicine, business
الوصف: Introduction 68Ga-DOTATATE is a radiolabeled peptide-based agonist that targets somatostatin receptors overexpressed in neuroendocrine tumors. Here, we present our results on validation of organic matrix 68Ge/68Ga generators (ITG GmbH) applied for radiosynthesis of the clinical doses of 68Ga-DOTATATE (GalioMedixTM). Methods The clinical grade of DOTATATE (25 μg ± 5 μg) compounded in 1 M NaOAc at pH = 5.5 was labeled manually with 514 ± 218 MBq (13.89 ± 5.9 mCi) of 68Ga eluate in 0.05 N HCl at 95 °C for 10 min. The radiochemical purity of the final dose was validated using radio-TLC. The quality control of clinical doses included tests of their osmolarity, endotoxin level, radionuclide identity, filter integrity, pH, sterility and 68Ge breakthrough. Results The final dose of 272 ± 126 MBq (7.35 ± 3.4 mCi) of 68Ga-DOTATATE was produced with a radiochemical yield (RCY) of 99% ± 1%. The total time required for completion of radiolabeling and quality control averaged approximately 35 min. This resulted in delivery of 50% ± 7% of 68Ga-DOTATATE at the time of calibration (not decay corrected). Conclusions 68Ga eluted from the generator was directly applied for labeling of DOTA-peptide with no additional pre-concentration or pre-purification of isotope. The low acidity of 68Ga eluate allows for facile synthesis of clinical doses with radiochemical and radionuclide purity higher than 98% and average activity of 272 ± 126 MBq (7.3 ± 3 mCi). There is no need for post-labeling C18 Sep-Pak purification of final doses of radiotracer. Advances in knowledge and implications for patient care. The clinical interest in validation of 68Galabeled agents has increased in the past years due to availability of generators from different vendors (Eckert-Ziegler, ITG, iThemba), favorable approach of U.S. FDA agency to initiate clinical trials, and collaboration of U.S. centers with leading EU clinical sites. The list of 68Ga-labeled tracers evaluated in clinical studies should growth because of the sensitivity of PET technique, the simplicity of the shakebake approach for the dose preparation and reliability of 68Ge/68Ga generators. Our studies have confirmed the reproducible elution profile, and high reliability of ITG GmbH generators required for routine doses preparation according to FDA recommendations.
تدمد: 0969-8051
URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_________::149594cf55edae9221c32387173a198f
https://doi.org/10.1016/j.nucmedbio.2015.08.004
حقوق: OPEN
رقم الأكسشن: edsair.doi...........149594cf55edae9221c32387173a198f
قاعدة البيانات: OpenAIRE