Acceptable and reproducible radiochemical purity (RP) for Ga-DOTATATE was difficult to obtain with the NETSPOT kit because the manufacturer instructions lacked details on the heater or needles used. The drug was prepared in an International Organization for Standardization (ISO) 5 environment. Multiple dry baths and needle types were used to investigate the effects of reaction temperature and metal contamination, respectively. Temperature curves were obtained with a calibrated thermocouple. The influence of the accuracy of the NETSPOT reagent volume and its effect on outcome were investigated. The AccuBlock dry bath required recalibration for the ISO 5 environment; after calibration, the temperature was stable (only ±0.1°C from the set point). When we followed package insert recommendations (dry bath temperature set to 98°C, reaction time of 8 min), the reaction temperature was 90.6°C. When Becton Dickinson needles were used for reconstitution, 15 of 18 runs (83%) did not meet the RP specification. However, B. Braun Medical needles achieved satisfactory and stable RP. When the Ga generator was eluted with 5.0 mL of 0.1 M hydrochloric acid (HCl), only 3.8-3.9 mL of eluate reached the reaction vial; this volume did not impact labeling (final pH was 3.8). The labeling success rate increased markedly if the Ga eluate was passed through a conditioned silica gel cartridge or if no cartridge was used; then, RP was more than 99%. HCl contact with the septum of the labeling vial reduced RP. The needle type and the temperature setting of the dry bath have critical roles in Ga-DOTATATE preparation. The AccuBlock dry bath has excellent stability and accuracy and can be used for reliable preparation. By using a conditioned silica gel cartridge or by eliminating the cartridge altogether, the RP is reliably high and stable.
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http://dx.doi.org/10.2967/jnmt.119.241224 | DOI Listing |
Bioresour Technol
December 2024
Department of Biotechnology, Sathyabama Institute of Science and Technology, Deemed to be University, Chennai 600 119, Tamil Nadu, India.
This study investigates the potentials of Chlorococcum humicolo algal biomass for the extraction of valuable biochemical and biodiesel production, with focus on the phycoremediation of textile dye effluents. The alga was cultivated in three media: CFTRI medium, combined dye effluent, and dye bath effluent in the laboratory. The highest cell count (254 × 10 cells/ml) and lowest oil content (16.
View Article and Find Full Text PDFInfluenza Other Respir Viruses
December 2024
Laboratory for Drug Discovery and Disease Research, Shionogi & Co, Ltd, Osaka, Japan.
Background: Evaluation of infectious virus titer is a challenge for respiratory syncytial virus (RSV) clinical trials because of the labile nature of RSV and rapid loss of infectivity without proper specimen handling. However, there has been no rigorous investigation into RSV stability in clinical specimens.
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Int J Biol Macromol
December 2024
Department of Chemical Engineering, University of Bath, Bath BA2 7AY, UK. Electronic address:
The demand for non-toxic, environmentally friendly, easily processable, water-resistant, flame-retardant and antimicrobial adhesives in the wood processing industry is becoming increasingly urgent. Few adhesives can possess these functions altogether while being synthesized easily. This paper presents a one-pot process utilizing corn starch, sodium hypochlorite, itaconic acid, and borax to synthesize a starch-based adhesive with dual crosslinking.
View Article and Find Full Text PDFPharm Res
October 2024
Pharmaceutical Surface Science Research Group, Department of Pharmacy & Pharmacology, University of Bath, Bath, UK.
Purpose: For locally-acting dry powder inhalers (DPIs), developing novel analytical tools that are able to evaluate the state of aggregation may provide a better understanding of the impact of material properties and processing parameters on the in vivo performance. This study explored the utility of the Morphologically-Directed Raman Spectroscopy (MDRS) and dissolution as orthogonal techniques to assess microstructural equivalence of the aerosolized dose of DPIs collected with an aerosol collection device.
Methods: Commercial DPIs containing different strengths of Fluticasone Propionate (FP) and Salmeterol Xinafoate (SX) as monotherapy and combination products were sourced from different regions.
Molecules
September 2024
Department of Chemistry, University of Bath, Claverton Down, Bath BA2 7AY, UK.
Protein therapeutics, vaccines, and other commercial products are often sensitive to environmental factors, such as temperature and long-term storage. In many cases, long-term protein stability is achieved by refrigeration or freezing. One alternative is the encapsulation of the protein cargo within an inert silica matrix (ensilication) and storage or transport at room temperature as a dry powder.
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