Dataset Information

Absorption, distribution, metabolism, and excretion of [14C]-labeled naloxegol in healthy subjects.

ABSTRACT: OBJECTIVE:To characterize the absorption, distribution, metabolism, and excretion of naloxegol, a PEGylated derivative of the µ-opioid antagonist naloxone, in healthy male subjects. MATERIALS AND METHODS:[14C]-Labeled naloxegol (27 mg, 3.43 MBq) was administered as an oral solution to 6 fasted subjects. Blood, fecal, and urine samples were collected predose and at various intervals postdose. Naloxegol and its metabolites were quantified or identified by liquid chromatography with radiometric or mass spectrometric detection. Pharmacokinetic parameters were calculated for each subject, and metabolite identification was performed by liquid chromatography with parallel radioactivity measurement and mass spectrometry. RESULTS:Naloxegol was rapidly absorbed, with a maximum plasma concentration (geometric mean) of 51 ng/mL reached before 2 hours after dosing. A second peak in the observed naloxegol and [14C] plasma concentration-time profiles was observed at ~3 hours and was likely due to enterohepatic recycling of parent naloxegol. Distribution to red blood cells was negligible. Metabolism of [14C]-naloxegol was rapid and extensive and occurred via demethylation and oxidation, dealkylation, and shortening of the polyethylene glycol chain. Mean cumulative recovery of radioactivity was 84.2% of the total dose, with ~68.9% recovered within 96 hours of dosing. Fecal excretion was the predominant route of elimination, with mean recoveries of total radioactivity in feces and urine of 67.7% and 16.0%, respectively. Unchanged naloxegol accounted for ~1/4 of the radioactivity recovered in feces. CONCLUSIONS:Naloxegol was rapidly absorbed and cleared via metabolism, with predominantly fecal excretion of parent and metabolites.

SUBMITTER: Bui K

PROVIDER: S-EPMC4564822 | biostudies-literature | 2015 Oct

REPOSITORIES: biostudies-literature

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Absorption, distribution, metabolism, and excretion of [14C]-labeled naloxegol in healthy subjects.

Bui Khanh K She Fahua F Hutchison Michael M Brunnström Åsa Å Sostek Mark M

International journal of clinical pharmacology and therapeutics 20151001 10

<h4>Objective</h4>To characterize the absorption, distribution, metabolism, and excretion of naloxegol, a PEGylated derivative of the µ-opioid antagonist naloxone, in healthy male subjects.<h4>Materials and methods</h4>[14C]-Labeled naloxegol (27 mg, 3.43 MBq) was administered as an oral solution to 6 fasted subjects. Blood, fecal, and urine samples were collected predose and at various intervals postdose. Naloxegol and its metabolites were quantified or identified by liquid chromatography with ...[more]

PMID: 26329350

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Dataset Information

Absorption, distribution, metabolism, and excretion of [14C]-labeled naloxegol in healthy subjects.

Publications

Absorption, distribution, metabolism, and excretion of [14C]-labeled naloxegol in healthy subjects.

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