Zobrazeno 1 - 10
of 78
pro vyhledávání: '"I. Al Jammaz"'
Publikováno v:
EJNMMI Radiopharmacy and Chemistry, Vol 6, Iss 1, Pp 1-17 (2021)
Abstract Background There is a need to develop new and more potent radiofluorinated peptide and their hybrid conjugates for multiple-receptors targeting properties that overexpress on many cancers. Methods We have synthesized MUC1-[18F] SFB and MUC1-
Externí odkaz:
https://doaj.org/article/0e770066d9024060a0a8dfe55ff4da16
Publikováno v:
Applied Radiation and Isotopes. 144:29-33
Myocardial perfusion imaging (MPI) is one of the most commonly performed investigations in nuclear medicine studies. Due to the physical properties of the positron emitter gallium-68 (68Ga) and its availability from 68Ge/68Ga generator, together with
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::54f78c093cf202519b873b533f48dd03
https://doi.org/10.1016/j.apradiso.2018.09.009
https://doi.org/10.1016/j.apradiso.2018.09.009
Publikováno v:
EJNMMI Radiopharmacy and Chemistry, Vol 6, Iss 1, Pp 1-17 (2021)
EJNMMI Radiopharmacy and Chemistry
EJNMMI Radiopharmacy and Chemistry
Background There is a need to develop new and more potent radiofluorinated peptide and their hybrid conjugates for multiple-receptors targeting properties that overexpress on many cancers. Methods We have synthesized MUC1-[18F] SFB and MUC1-FA-[18F]
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5c5cfc2f53828d0276c41a4f9834d007
https://doi.org/10.21203/rs.3.rs-47894/v1
https://doi.org/10.21203/rs.3.rs-47894/v1
Akademický článek
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Publikováno v:
Journal of Labelled Compounds and Radiopharmaceuticals. 54:312-317
In an attempt to simplify nucleophilic radiofluorination reactions to be amenable for automation, a series of [18F]fluoronicotinamides, [18F]fluoroisonicotinamides and [18F]fluorobenzamides were synthesized using one-step synthetic approach involving
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::51c862078403364b994ae80d8b2f74ac
https://doi.org/10.1002/jlcr.1869
https://doi.org/10.1002/jlcr.1869
Autor:
I. Al Jammaz, S. Al-Yanbawi
Publikováno v:
Radiochimica Acta. 95:657-661
The production yield of iodine radionuclides (123/124I) by solid target irradiation strongly depends on the quality of the tellurium (Te) target. To avoid poor quality 124Te targets frequently obtained using the classical method, a new technology for
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::065c915e6ebc0186984465f627190df5
https://doi.org/10.1524/ract.2007.95.11.657
https://doi.org/10.1524/ract.2007.95.11.657
Publikováno v:
Journal of Labelled Compounds and Radiopharmaceuticals. 49:125-137
In an attempt to visualize folate receptors that over-express on many cancers, [18F]-fluorobenzene and pyridine carbohydrazide-folates were synthesized using two different synthetic approaches starting from nucleophilic displacement reactions on ethy
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::23caad84035c5d94f79d18818a248c93
https://doi.org/10.1002/jlcr.1022
https://doi.org/10.1002/jlcr.1022
Publikováno v:
Nuclear Medicine and Biology. 29:817-823
2-[18F]-Fluoroisonicotinic acid hydrazide was synthesized by nucleophilic displacement reaction on ethyl-2- (trimethylammonium)-isonicotinate precursor in acetonitrile. Kryptofix 222 was used as the phase transfer catalyst. The intermediate fluorinat
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f09869018d9053c6eb7c60fbe0698f01
https://doi.org/10.1016/s0969-8051(02)00340-2
https://doi.org/10.1016/s0969-8051(02)00340-2
Publikováno v:
Journal of Labelled Compounds and Radiopharmaceuticals. 44:S451-S454
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::475f9de7b8c6f5e4d378aa9c0ad7d49b
https://doi.org/10.1002/jlcr.25804401159
https://doi.org/10.1002/jlcr.25804401159
Publikováno v:
Applied Radiation and Isotopes. 54:711-714
The increasing demand for radiolabeled metaiodobenzylguanidine (mIBG) prompted the need to obtain the radiopharmaceutical by a reliable, routine and simple synthetic method for batch production. The production of mIBG labeled with either 123 I or 124
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::cda0ea3cc2f9fa276c26c64b12641e3a
https://doi.org/10.1016/s0969-8043(00)00340-7
https://doi.org/10.1016/s0969-8043(00)00340-7