|Toxicokinetics and biotransformation of p-nitrophenol in red abalone (Haliotis rufescens)|
TenBrook, P.L.; Kendall, S.M.; Viant, M.R.; Tjeerdema, R.S. (2003). Toxicokinetics and biotransformation of p-nitrophenol in red abalone (Haliotis rufescens). Aquat. Toxicol. 62(4): 329-336
In: Aquatic Toxicology. Elsevier Science: Tokyo; New York; London; Amsterdam. ISSN 0166-445X, more
|Authors|| || Top |
- TenBrook, P.L.
- Kendall, S.M.
- Viant, M.R.
- Tjeerdema, R.S.
Red abalone (Haliotis rufescens) were exposed to 3.6 µM (0.5 ppm) 14C-labelled p-nitrophenol (PNP) for 24 h, then were allowed to depurate in clean seawater for another 24 h. Absorption, conditional uptake clearance and elimination rate constants were 0.12±0.04 h-1, 3.2±1.1 ml g-1 h-1 and 0.05±0.02 h-1, respectively. The sigmoidal shape of the PNP uptake curve suggests a biphasic process. A whole-organism total concentration factor (TCF) of 2.37±0.07 was determined from equilibrium tissue and water concentrations, with the highest concentration of PNP plus metabolites found in gill tissue (11.8±0.2 nmol g-1, wet weight). Digestive gland, foot muscle and remaining body tissues accumulated 8.8±0.9, 7.7±0.6 and 7.5±0.6 nmol g-1 radiolabelled residues, respectively. Abalone depurated 91.6% of absorbed PNP within 24 h, of which 87.5±3.1% was unmetabolized parent compound, 13.1±3.1% was p-nitrophenylsulfate, 0.32±0.09% was p-nitroanisole, and 0.14±0.07% was p-acetamidophenol.