Pyridoxine (vitamin B 6 , VB 6) was detected in pharmaceutical preparation and human urine samples by employing differential pulse voltammetry (DPV) at unmodified boron doped electrode. In Britton-Robinson buffer solution (BRBS) at pH 6 VB 6 provides well defined oxidation peak at around +1.05 V vs. Ag/AgCl (3M KCl). The influence of most of the interferents present in real samples, supporting electrolyte and DPV parameters were investigated. A VB 6 sensor with and linear range from 7 to 47 and a detection limit of 3.76 was obtain after optimization. Repeatability of the proposed procedure calculated after 7 measurements of 9 and 30 µM of VB 6 were 3.6 and 2.4 %, respectively. Proposed methodology was successfully applied for the determination of VB 6 in real samples, and from obtained results it can be concluded that proposed analytical procedure can be inexpensive alternative to the widely used separation methods.
10 and 20 mg of N-Propyl-ajmalin-hydrogentartrate (N-PAB, Neo-Gilurytmal) were administered i.v. and orally respectively to healthy volunteers. In the study 14C-labelled N-PAB was used. The pharmacokinetics and the metabolic behaviour was examined. A fast and complete absorption of the compound could be observed. The bioavailability was 78%. The terminal plasma elimination half-life (beta-phase) was in the range of 4 to 6 hours. A total of 33% of the administered radioactivity was excreted via the kidney. 35 to 48% of the radioactivity found in urine was unchanged N-PAB. The excretion-kinetics of the three main metabolites as well as of the parent compound were determined. The possible presence of non-metabolizers is suggested.
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