Gas chromatography nitrogen phosphorous detection (GC-NPD) assay of tofisopam in human plasma for pharmacokinetic evaluation
Autor: | Andrea Bereczki, Judit Tömlo, Katalin Balogh Nemes, Géza Lakner, Mária Tóth, Sándor Drabant, Imre Klebovich, G. Grézal, Bálint Varga |
---|---|
Rok vydání: | 2006 |
Předmět: |
Adult
Male Bioanalysis Chromatography Gas Clinical Biochemistry Pharmaceutical Science Absorption (skin) Analytical Chemistry Benzodiazepines Pharmacokinetics Drug Discovery Blood plasma medicine Humans Distribution (pharmacology) Sample preparation Spectroscopy Chromatography Chemistry Reproducibility of Results Tofisopam Antidepressive Agents Area Under Curve Gas chromatography Half-Life medicine.drug |
Zdroj: | Journal of Pharmaceutical and Biomedical Analysis. 41:1354-1359 |
ISSN: | 0731-7085 |
DOI: | 10.1016/j.jpba.2006.03.033 |
Popis: | Tofisopam (1-(3,4-dimethoxyphenyl)-4-methyl-5-ethyl-7,8-dimethoxy-5H-2,3-benzodiazepine) has been shown to be an effective anxiolytic agent in the wide-ranging clinical practice. A high sensitive gas chromatography nitrogen phosphorous detection (GC-NPD) bioanalytical method was developed and validated for the purpose of pharmacokinetic study of tofisopam. A liquid–liquid extraction method was used for the sample preparation. The mean recovery for tofisopam was 69.8% and the inter- and intra-day precision values were well below the 15% limit established for bioanalytical methods. A similar compound, girizopam was used as internal standard. The assay was linear in the 5–500 ng/ml range corresponding to therapeutically relevant plasma levels. The concentrations of the compound were measured in the plasma samples of 12 healthy male volunteers and the pharmacokinetic parameters were determined from the plasma concentration–time data. A rapid absorption and distribution, relatively short biological half-life and considerable inter-individual variation in the plasma concentration levels of parent compound were the main characteristics of the pharmacokinetics of tofisopam. According to these results, the new (GC-NPD) bioanalytical method proved to be capable of measuring concentration of tofisopam in human plasma and was successfully applied in a single dose pharmacokinetic study. |
Databáze: | OpenAIRE |
Externí odkaz: |