Comparison of pharmacokinetics and relative bioavailability of tablets and substance of new dipeptide neuroleptic dilept
- PMID: 25348562
- DOI: 10.1007/s10517-014-2655-1
Comparison of pharmacokinetics and relative bioavailability of tablets and substance of new dipeptide neuroleptic dilept
Abstract
We studied pharmacokinetics of dilept after single cross-administration of tablets and substance of dilept in a dose of 40 mg to rabbits. The following pharmacokinetic parameters were calculated: maximum plasma concentration of dilept, time to maximum observed concentration, area under the pharmacokinetic curve, elimination half-life, and relative bioavailability. Dilept concentration in blood plasma was estimated using ultra-fast liquid chromatography with mass spectrometry detection. Relative bioavailability of dilept tablets was 93.46±28.91% of that for the substance.
Publication types
MeSH terms
Substances
LinkOut - more resources
Full Text Sources
Other Literature Sources
