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Metabolic disposition of the anti-cancer agent [(14)C]laromustine in male rats.

Abstract
1. Laromustine (VNP40101M, also known as Cloretazine) is a novel sulfonylhydrazine alkylating (anticancer) agent. This article describes the use of quantitative whole-body autoradiography (QWBA) and mass balance to study the tissue distribution, the excretion mass balance and pharmacokinetics after intravenous administration of [(14)C]VNP40101M to rats. A single 10 mg/kg IV bolus dose of [(14)C]VNP40101M was given to rats. 2. The recovery of radioactivity from the Group 1 animals over a 7-day period was an average of 92.1% of the administered dose, which was accounted for in the excreta and carcass. Most of the radioactivity was eliminated within 48 h via urine (48%), with less excreted in feces (5%) and expired air accounted for (11%). The plasma half-life of [(14)C]laromustine was approximately 62 min and the peak plasma concentration (Cmax) averaged 8.3 μg/mL. 3. The QWBA study indicated that the drug-derived radioactivity was widely distributed to tissues through 7 days post-dose after a single 10 mg/kg IV bolus dose of [(14)C]VNP40101M to male pigmented Long-Evans rats. The maximum concentrations were observed at 0.5 or 1 h post-dose for majority tissues (28 of 42). The highest concentrations of radioactivity were found in the small intestine contents at 0.5 h (112.137 µg equiv/g), urinary bladder contents at 3 h (89.636 µg equiv/g) and probably reflect excretion of drug and metabolites. The highest concentrations in specific organs were found in the renal cortex at 1 h (28.582 µg equiv/g), small intestine at 3 h (16.946 µg equiv/g), Harderian gland at 3 h (12.332 µg equiv/g) and pancreas at 3 h (12.635 µg equiv/g). Concentrations in the cerebrum (1.978 µg equiv/g), cerebellum (2.109 µg equiv/g), medulla (1.797 µg equiv/g) and spinal cord (1.510 µg equiv/g) were maximal at 0.5 h post-dose and persisted for 7 days. 4. The predicted total body and target organ exposures for humans given a single 100 µCi IV dose of [(14)C]VNP40101M were well within the medical guidelines for maximum radioactivity exposures in human subjects.
AuthorsAla F Nassar, Adam Wisnewski, Ivan King
JournalXenobiotica; the fate of foreign compounds in biological systems (Xenobiotica) Vol. 45 Issue 8 Pg. 711-21 ( 2015) ISSN: 1366-5928 [Electronic] England
PMID25798740 (Publication Type: Journal Article)
Chemical References
  • Antineoplastic Agents
  • Hydrazines
  • Metalloporphyrins
  • Sulfonamides
  • iron chlorin e(6)
  • laromustine
Topics
  • Animals
  • Antineoplastic Agents (administration & dosage, blood, pharmacokinetics, urine)
  • Humans
  • Hydrazines (administration & dosage, blood, pharmacokinetics, urine)
  • Injections, Intravenous
  • Male
  • Metalloporphyrins (chemistry)
  • Models, Animal
  • Neoplasms (drug therapy)
  • Rats
  • Rats, Long-Evans
  • Rats, Sprague-Dawley
  • Sulfonamides (administration & dosage, blood, pharmacokinetics, urine)
  • Tissue Distribution

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