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The influence of isotopic and nonisotopic carriers on the biodistribution and biokinetics of M3+-citrate complexes.

Identifieur interne : 000811 ( PubMed/Checkpoint ); précédent : 000810; suivant : 000812

The influence of isotopic and nonisotopic carriers on the biodistribution and biokinetics of M3+-citrate complexes.

Auteurs : K. Schom Cker ; W G Franke ; E. Henke ; W D Fromm ; G. Maka ; G J Beyer

Source :

RBID : pubmed:3456891

Descripteurs français

English descriptors

Abstract

The influence of carrier amounts of Fe, Ga, and Tm on the biodistribution of 67Ga-, 59Fe-, and 167Tm-citrate in mice was investigated. Our results suggest that 167Tm, unlike 67Ga and 59Fe, is not transported by transferrin in the blood. Of the three radioisotopes tested, 167Tm had the highest tumor/background ratio (10 h after the injection). The application of Fe carrier led to an enhancement of the elimination of 67Ga from the blood and muscles, resulting in a better tumor/background ratio.

PubMed: 3456891


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pubmed:3456891

Le document en format XML

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<div type="abstract" xml:lang="en">The influence of carrier amounts of Fe, Ga, and Tm on the biodistribution of 67Ga-, 59Fe-, and 167Tm-citrate in mice was investigated. Our results suggest that 167Tm, unlike 67Ga and 59Fe, is not transported by transferrin in the blood. Of the three radioisotopes tested, 167Tm had the highest tumor/background ratio (10 h after the injection). The application of Fe carrier led to an enhancement of the elimination of 67Ga from the blood and muscles, resulting in a better tumor/background ratio.</div>
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