Compatibility of [99mTc]Tc-EDDA/HYNIC-TOC and [68Ga] Ga-DOTA-TOC in a syringe for intravenous administration

Autor: Philip Chennell, Sarah Chaib, Isabelle Morelec, Caroline Darcissac, Catherine Rioufol, Valérie Sautou, F. Hallouard, Marc Fraysse
Přispěvatelé: Laboratoire de Pharmacie Galenique, Biopharmacie et Pharmacie Clinique, Université de Rennes 1 (UR1), Université de Rennes (UNIV-RENNES)-Université de Rennes (UNIV-RENNES), Institut de Chimie de Clermont-Ferrand (ICCF), SIGMA Clermont (SIGMA Clermont)-Institut de Chimie du CNRS (INC)-Université Clermont Auvergne [2017-2020] (UCA [2017-2020])-Centre National de la Recherche Scientifique (CNRS), CHU Clermont-Ferrand, Ciblage thérapeutique en Oncologie (EA3738), Université Claude Bernard Lyon 1 (UCBL), Université de Lyon-Université de Lyon, Unité de Radiopharmacie - Service de Pharmacie [Pierre-Bénite], Centre Hospitalier Lyon Sud [CHU - HCL] (CHLS), Hospices Civils de Lyon (HCL)-Hospices Civils de Lyon (HCL), Laboratoire de Pharmacie Galenique, Biopharmacie et Pharmacie Clinique [Rennes], Université de Rennes (UR)
Jazyk: angličtina
Rok vydání: 2020
Předmět:
Zdroj: Nuclear Medicine Communications
Nuclear Medicine Communications, Lippincott, Williams & Wilkins, 2020, 41 (1), pp.11-17. ⟨10.1097/MNM.0000000000001108⟩
Nuclear Medicine Communications, 2020, 41 (1), pp.11-17. ⟨10.1097/MNM.0000000000001108⟩
ISSN: 0143-3636
Popis: International audience; Objective Drug quality in medical devices is not evaluated during the marketing authorization of radiopharmaceuticals. Therefore, the extemporaneous change of packaging made for preparation of patient unit doses in a syringe is the responsibility of radiopharmacists. The present study aimed to determine the impact of packaging and storage in a polypropylene syringe on the quality of hydrophilic drugs [99mTc]Tc-EDDA/HYNIC-TOC (Tektrotyd) and [68Ga]Ga-DOTA-TOC (Somakit-TOC).Methods Appearance, pH, radiochemical purity, sterility, and endotoxin tests were performed according the current European Pharmacopoeia. Subvisible and visible particles tests of the European Pharmacopoeia were adapted due to limited preparation volume (
Databáze: OpenAIRE