Awards Nomination 20+ Million Readerbase
Indexed In
  • Academic Journals Database
  • Open J Gate
  • Genamics JournalSeek
  • Academic Keys
  • JournalTOCs
  • China National Knowledge Infrastructure (CNKI)
  • CiteFactor
  • Scimago
  • Ulrich's Periodicals Directory
  • Electronic Journals Library
  • RefSeek
  • Hamdard University
  • EBSCO A-Z
  • OCLC- WorldCat
  • SWB online catalog
  • Virtual Library of Biology (vifabio)
  • Publons
  • MIAR
  • University Grants Commission
  • Geneva Foundation for Medical Education and Research
  • Euro Pub
  • Google Scholar
Share This Page
Journal Flyer
Journal of Bioequivalence & Bioavailability

Miroslav Ryska

Miroslav Ryska

Czech Republic

Publications
  • Research Article
    The Pharmacokinetic Properties and Bioequivalence of Methyldopa Formulations: Results of an Open-label, Randomized, Two-period, Crossover, Single-dose Study
    Author(s): Alexander Leonidovich Khokhlov, Leonid Nikolaevich Shitov, Miroslav Ryska, Yuriy Aleksandrovich Dzhurko, Vladimír Kube&scaron, Vitaliy Nikolaevich Shabrov, Aleksey Evgenyevich Miroshnikov, Elena Valeryevna Korneva, Anna Vitalyevna Demchinskaya, Anastasiya Mikhailovna Shitova, Igor Evgenyevich Shokhin and Elena Georgievna LileevaAlexander Leonidovich Khokhlov, Leonid Nikolaevich Shitov, Miroslav Ryska, Yuriy Aleksandrovich Dzhurko, Vladimír Kube&scaron, Vitaliy Nikolaevich Shabrov, Aleksey Evgenyevich Miroshnikov, Elena Valeryevna Korneva, Anna Vitalyevna Demchinskaya, Anastasiya Mikhailovna Shitova, Igor Evgenyevich Shokhin and Elena Georgievna Lileeva

    Comparative assessment of the pharmacokinetic properties and bioequivalence (BE) of two methyldopa formulations (Methyldopa, 250 mg tablets, R-Pharm CJSC, Russia-investigational medicinal product, and Dopegyt®, 250 mg tablets, EGIS Pharmaceuticals PLC, Hungary-reference product) were investigated in 24 healthy volunteers (13 women and 11 men, caucasian) in an open-label, randomized, crossover, two-period, two-sequence trial with 7-day washout period. A comparative dissolution test was carried out in advance in 3 media, including quantitative determination of methyldopa by UV spectrophotometry. The release patterns of the active ingredient from the test and reference products were equivalent. Methyldopa concentrations in plasma were measured by validated method of high-performance liquid chromatography-tandem mass spectrometry, using the deuterated internal standard. The validation.. View More»

    Abstract PDF