Pharmacokinetics of pemoline in plasma, saliva and urine following oral administration

Br J Clin Pharmacol. 1979 Nov;8(5):459-63. doi: 10.1111/j.1365-2125.1979.tb01026.x.

Abstract

1 Pemoline concentrations were measured in plasma and saliva following a single oral dose (37.5 or 50.0 mg) to healthy volunteers. In addition urinary excretion rates and cumulative urinary excretion of the parent compound and its oxazolidinedione metabolite were determined. 2 The plasma curves exhibited a mean elimination half-live of 11.0 +/- 1.2 h (n=4). Peak levels were reached at 2.7 +/- 0.6 h (n=4). The saliva concentrations were about 50% lower than the corresponding plasma concentrations during the elimination phase. During the absorption phase irregularities in the saliva to plasma concentration ratios were observed. 3 In urine 47.0 +/- 8.4% of the dose (n=6) administered was excreted as unchanged drug and only 3.7 +/- 0.8% (n=3) as the oxazolidinedione metabolite. Urinary half-lives were slightly shorter than the corresponding plasma half-lives.

MeSH terms

  • Administration, Oral
  • Adult
  • Humans
  • Male
  • Pemoline / administration & dosage
  • Pemoline / blood
  • Pemoline / metabolism*
  • Pemoline / urine
  • Saliva / metabolism*
  • Time Factors

Substances

  • Pemoline