|
|
||||||||
Pharmazeutisches Institut der Freien Universität Berlin
Correspondence: For reprints contact: M. Wenzel, Freie Universität, #D 1 Berlin-Dahlem, Königin-Luise-Str. 2-4, Germany.
ABSTRACT
Metalocene carboxylic acids labeled with 59Fe or 103Ru were administered to mice and the organ distributions and amounts of label excreted were determined. Both metalocenes were excreted approximately 90 times faster than the respective inorganic chlorides 59FeCl3 or 103RuCl3. The metalocenes showed an extremely high kidney-to-muscle ratio (up to 1,000). 99mTc-labeled renal agents, tested for comparison, showed lower ratios. Retention of radioactivity in blood and the presence of free iron in urine indicate that the ferrocene derivative is degraded in vivo, but the ruthenocene analog is not.
This article has been cited by other articles:
![]() |
E. E. Cable and H. C. Isom Metabolism of 3,5,5-Trimethylhexanoyl-Ferrocene by Rat Liver: Release of Iron from 3,5,5-Trimethylhexanoyl-Ferrocene by a Microsomal, Phenobarbital-Inducible Cytochrome P-450 Drug Metab. Dispos., February 1, 1999; 27(2): 255 - 260. [Abstract] [Full Text] |
||||
| HOME | HELP | FEEDBACK | SUBSCRIPTIONS | ARCHIVE | SEARCH | TABLE OF CONTENTS |
| JOURNAL OF NUCLEAR MEDICINE TECHNOLOGY | THE JOURNAL OF NUCLEAR MEDICINE |