Table 4

Analysis of metabolites in excreta 24 h after administration of [14C]1,2-DEB to male Sprague-Dawley rats4-a

TreatmentPercentage of the Sample Radioactivity
Route of AdministrationDoseAnimalExcretaFraction 14-a1,2-DEBEPEFraction 24-aGA1GA2Ratio GA1/GA2
mg/kg b.wt.
i.v.1non bile duct-cannulatedurine9.4  ± 0.9<0.11.682.4  ± 1.221.640.10.5
(n = 5)feces27.9  ± 1.6<0.119.918.9  ± 0.6<0.11.1
i.v.1bile duct-cannulatedurine7.3  ± 1.6<0.11.179.3  ± 4.135.543.40.8
(n = 3)bile4.0  ± 0.0<0.11.088.8  ± 0.41648.50.3
Oral100non bile duct-cannulatedurine6.6  ± 0.4<0.11.681.6  ± 1.12036.90.5
(n = 5)feces25.5  ± 2.56.612.510.4  ± 3.4<0.1<0.1
Oral100bile duct-cannulatedurine2.7  ± 0.1<0.10.384.0  ± 0.425.131.80.8
(n = 3)bile3.4  ± 0.4<0.11.693.9  ± 1.127.547.40.6

Urine, bile, or feces were collected on a 0- to 24-h period. For each sample, neutral (fraction 1) and acidic (fraction 2) metabolites were separated as described in Materials and Methods. The radioactivity content was measured on an aliquot of each fraction. Then, aliquots of each fraction from the same treatment were pooled and EPE, GA1, and GA2 metabolites of [14C]DEB were quantified by HPLC.

  • 4-a Data expressed as mean ± S.E.