Dthm. Sijm et al., ETHYL M-AMINOBENZOATE METHANESULFONATE DEPENDENT AND CARRIER DEPENDENT PHARMACOKINETICS OF EXTREMELY LIPOPHILIC COMPOUNDS IN RAINBOW-TROUT, Archives of environmental contamination and toxicology, 25(1), 1993, pp. 102-109
Significant differences were found in both uptake and pharmacokinetics
in fish when six lipophilic compounds were dosed by gavage in either
an oil or an gelatin carrier. Pharmacokinetics were also different whe
n fish were anaesthetized with ethyl m-aminobenzoate methanesulfonate
(MS-222) before dosing. The highest uptake percentages, uptake rates a
nd concentrations of the compounds were found in the fish which were g
iven the gelatin carrier only. MS-222 decreased the uptake of the comp
ounds. Absorption of the compounds from oil was lower than from gelati
n. In addition, absorption from oil continued for 21 d, which lasted l
onger than from gelatin. In the fish which were given the gelatin, the
concentrations of the compounds in both muscle and liver showed a com
pound dependent decrease in the course of the experiment. In general,
in all treatments higher concentrations were found in liver than in mu
scle. For each treatment, the absorption rates of pentachlorobenzene,
hexachlorobenzene, 2,2',5,5'-tetrachlorobiphenyl and 2,2',4,4',5,5'-he
xachlorobiphenyl were similar, but different from the other treatments
. It can be concluded that the experimental methodology significantly
affects the pharmacokinetic parameters that are used to model the bioc
oncentration of hydrophobic chemicals in the environment.