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18F-fluoromisonidazole

F-fluoromisonidazole [81] in hypoxic tissue have led to the development of such an agent based on 99mTc, All of these studies to date have involved the incorporation of the 2-nitroimidazole function onto a known stable complex for technetium. [Pg.141]

PET imaging using 8F-fluoromisonidazole (FMISO) and 18F-fluoroazomycinarabinofuranoside (FAZA) is well established for human application, allowing the measurement of hypoxia status. Their limitations include poor availability of the radiolabeled product and short lifetime of the 18F PET isotope (half life ca. 110 min). [Pg.151]

Hara T, Yuasa M (1999). Automated synthesis of [nC] Choline, a positron-emitting tracer for tumor imaging. Appl Radiat Isot 50 531 Huisman MC, Higuchi T, Reder S et al (2008). Initial characterization of an 18F-labled myocardial perfusion tracer. J Nucl Med 49 630 Kabalka GW, Lambrecht RM, Fowler JS et al (1985). Synthesis of 150-labelled butanol via organoborane chemistry. Appl Radiat Isot 36 853 Kamarainen EL, Kyllonen T, Nihtila O et al (2004). Preparation of fluorine-18 labeled fluoromisonidazole using two different synthesis methods. J Labeled Comp Radiopharm 47 37... [Pg.149]


See other pages where 18F-fluoromisonidazole is mentioned: [Pg.52]    [Pg.39]    [Pg.135]    [Pg.166]    [Pg.52]    [Pg.39]    [Pg.135]    [Pg.166]    [Pg.165]    [Pg.166]   
See also in sourсe #XX -- [ Pg.151 ]




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