The aim of this study was to determine in vitro protein binding of tolterodine and its 5-hydroxymethyl (5-HM) and N-dealkylated metabolites in serum from humans and several animal species at concentrations similar to those obtained in clinical and preclinical studies. Binding of tolterodine and the
Toxicokinetics of ochratoxin A in several species and its plasma-binding properties
β Scribed by Sigrid Hagelberg; Karl Hult; Radovan Fuchs
- Publisher
- John Wiley and Sons
- Year
- 1989
- Tongue
- English
- Weight
- 549 KB
- Volume
- 9
- Category
- Article
- ISSN
- 0260-437X
No coin nor oath required. For personal study only.
β¦ Synopsis
The toxicokinetic profile of ochratoxin A was studied after the oral or intravenous administration of 50 nglg b.w. to fish, quail, mouse, rat and monkey. The elimination half-life varied from 0.68 h after oral administration to fish, up to 840 h after intravenous administration to monkey. The distribution volume ranged from 57 ml/ kg in fish to 1500 ml/kg in quail. The plasma clearance was most rapid in quail and fish, 72 and 58 ml/kg.h, respectively, while it was only 0.17 ml/kg.h in monkey. The bioavailability was as low as 1.6% in fish but a5 high as 97% in mouse.
The binding abilities of ochratoxin A to plasma proteins were also studied. From these data we calculated the free fraction of toxin in plasma, which we found to be < 0.2% in all species investigated (including man) except fish.
A similar but smaller investigation on the toxicokinetics and binding properties of ochratoxin B was also performed. Ochratoxin B was more readily eliminated and had a lower affinity for plasma proteins, which partly may explain its lower toxicity.
Experimental animals
Five different animal species were used in the excretion study: fish, quail, mouse, rat and monkey. No control
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