1. Human urinary excretion of NC100692, an RGD-peptide for imaging angiogenesis
- Author
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Inger Oulie, Tore Skotland, Line Roed, and B.J. McParland
- Subjects
Adult ,Male ,Chromatography ,Neovascularization, Pathologic ,Chemistry ,Angiogenesis ,Urinary system ,Technetium ,Pharmaceutical Science ,Urine ,Metabolism ,Peptides, Cyclic ,High-performance liquid chromatography ,Mass Spectrometry ,Radiography ,Excretion ,Freeze Drying ,Pharmacokinetics ,Liquid chromatography–mass spectrometry ,Humans ,Female ,Single-Blind Method ,Radiopharmaceuticals ,Oligopeptides ,Chromatography, High Pressure Liquid - Abstract
The (99m)Tc complex of NC100692 is being evaluated as a diagnostic agent for the detection of angiogenesis. In the present study, human urine samples from a clinical Phase I study were analysed using reversed-phase liquid chromatography coupled with an ion-trap mass spectrometer (LC-MS) in order to estimate the amount of intact NC100692 and any metabolites excreted in urine following intravenous injection of 150microg (99m)Tc-NC100692. Only intact NC100692 was observed in these urine samples, no metabolites were detected, in contrast to data earlier reported for rat urine where two metabolites and no NC100692 were observed. Within 4-8h after injection, 30+/-6% of the injected NC100692 was excreted in the urine, with the majority (23+/-5%) recovered within the first hour post-injection. There was good agreement between the calculated urinary recoveries of NC100692 and total radioactivity in urine samples voided approximately 1h post-injection. NC100692 constituting 98+/-24% of the total urinary (99m)Tc recovery indicating that the (99m)Tc excreted during this period was most likely excreted as (99m)Tc-NC100692. The ratio of NC100692 to (99m)Tc decreased in the urine samples as a function of time following injection for all subjects; this change is most likely due to reduced accuracy in the results at low levels of NC100692.
- Published
- 2009
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