scholarly journals 18F[AlF]-radiolabelled Peptides on the Automated Synthesis Platform: Translating the Laboratory Bench Work to Bedside

2019 ◽  
Vol 26 (4) ◽  
pp. 122-126
Author(s):  
Hishar Hassan ◽  
◽  
Hairil Rashmizal Abdul Razak ◽  
Fathinul Fikri Ahmad Saad ◽  
Vijay Kumar ◽  
...  
2009 ◽  
Vol 2 (3) ◽  
pp. 199-213
Author(s):  
Vikash Kumar ◽  
Permender Rathee ◽  
Kanchan Kohli ◽  
Hema Chaudhary ◽  
Sushila Rathee

1993 ◽  
Vol 58 (s1) ◽  
pp. 204-208 ◽  
Author(s):  
Andres Jäschke ◽  
Jens P. Fürste ◽  
Dieter Cech ◽  
Volker A. Erdmann

2019 ◽  
Vol 61 (6) ◽  
pp. 748-753
Author(s):  
D. O. Antuganov ◽  
D. V. Ryzhkova ◽  
V. V. Timofeev ◽  
T. A. Zykova ◽  
Yu. O. Antuganova ◽  
...  

Author(s):  
Vanessa Ribeiro Urbano ◽  
Milena Guedes Maniero ◽  
José Roberto Guimarães ◽  
Luis J. del Valle ◽  
Montserrat Pérez-Moya

Sulfaquinoxaline (SQX) has been detected in environmental water samples, where its side effects are still unknown. To the best of our knowledge, its oxidation by Fenton and photo-Fenton processes has not been previously reported. In this study, SQX oxidation, mineralization, and toxicity (Escherichia coli and Staphylococcus aureus bacteria) were evaluated at two different setups: laboratory bench (2 L) and pilot plant (15 L). The experimental design was used to assess the influence of the presence or absence of radiation source, as well as different H2O2 concentrations (94.1 to 261.9 mg L−1). The experimental conditions of both setups were: SQX = 25 mg L−1, Fe(II) = 10 mg L−1, pH 2.8 ± 0.1. Fenton and photo-Fenton were suitable for SQX oxidation and experiments resulted in higher SQX mineralization than reported in the literature. For both setups, the best process was the photo-Fenton (178.0 mg L−1 H2O2), for which over 90% of SQX was removed, over 50% mineralization, and bacterial growth inhibition less than 13%. In both set-ups, the presence or absence of radiation was equally important for sulfaquinoxaline oxidation; however, the degradation rates at the pilot plant were between two to four times higher than the obtained at the laboratory bench.


2017 ◽  
Vol 45 (1) ◽  
pp. 661-675
Author(s):  
Daniel Lustig ◽  
Andrew Wright ◽  
Alexandros Papakonstantinou ◽  
Olivier Giroux

Author(s):  
Anup Gangwar ◽  
Nitin Kumar Agarwal ◽  
Ravishankar Sreedharan ◽  
Ambica Prasad ◽  
Sri Harsha Gade ◽  
...  

2020 ◽  
pp. 437-456
Author(s):  
Laura Bruton ◽  
Peter J.H. Scott
Keyword(s):  

Biomolecules ◽  
2021 ◽  
Vol 11 (8) ◽  
pp. 1118
Author(s):  
Emma Jussing ◽  
Stefan Milton ◽  
Erik Samén ◽  
Mohammad Mahdi Moein ◽  
Lovisa Bylund ◽  
...  

By using solid targets in medical cyclotrons, it is possible to produce large amounts of 68GaCl3. Purification of Ga3+ from metal ion impurities is a critical step, as these metals compete with Ga3+ in the complexation with different chelators, which negatively affects the radiolabeling yields. In this work, we significantly lowered the level of iron (Fe) impurities by adding ascorbate in the purification, and the resulting 68GaCl3could be utilized for high-yield radiolabeling of clinically relevant DOTA-based tracers. 68GaCl3 was cyclotron-produced and purified with ascorbate added in the wash solutions through the UTEVA resins. The 68Ga eluate was analyzed for radionuclidic purity (RNP) by gamma spectroscopy, metal content by ICP-MS, and by titrations with the chelators DOTA, NOTA, and HBED. The 68GaCl3eluate was utilized for GMP-radiolabeling of the DOTA-based tracers DOTATOC and FAPI-46 using an automated synthesis module. DOTA chelator titrations gave an apparent molar activity (AMA) of 491 ± 204 GBq/µmol. GMP-compliant syntheses yielded up to 7 GBq/batch [68Ga]Ga-DOTATOC and [68Ga]Ga-FAPI-46 (radiochemical yield, RCY ~ 60%, corresponding to ten times higher compared to generator-based productions). Full quality control (QC) of 68Ga-labelled tracers showed radiochemically pure and stable products at least four hours from end-of-synthesis.


1980 ◽  
Vol 11 (3-4) ◽  
pp. 45-53
Author(s):  
R. A. Mueller
Keyword(s):  

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