Zobrazeno 1 - 5
of 5
pro vyhledávání: '"M. V. Velikopol'skaya"'
Autor:
A. A. Spasov, A. F. Kucheryavenko, K. A. Gaidukova, V. S. Sirotenko, L. A. Smirnova, A. F. Ryabukha, K. A. Kuznetsov, M. V. Velikopol’skaya
Publikováno v:
Pharmaceutical Chemistry Journal. 56:1024-1026
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::96cc68d4aa226a0bc72f80165a53e9db
https://doi.org/10.1007/s11094-022-02746-4
https://doi.org/10.1007/s11094-022-02746-4
Autor:
Alexander A. Spasov, A. F. Ryabukha, K. A. Kuznetsov, M. V. Velikopol’skaya, D. S. Yakovlev, L. A. Smirnova
Publikováno v:
Pharmaceutical Chemistry Journal. 55:312-314
A quantitative determination method for drug substance RU-31, a derivative of a methoxyphenylimidazo - [1,2-α]benzimidazole possessing antimigraine activity, in biological samples was developed. This method has selectivity and high sensitivity suffi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::2251e7a516a28cc35ac63f4120be41b5
https://doi.org/10.1007/s11094-021-02418-9
https://doi.org/10.1007/s11094-021-02418-9
Autor:
D. S. Yakovlev, Alexander A. Spasov, K. A. Kuznetsov, M. V. Velikopol’skaya, A. F. Ryabukha, L. A. Smirnova
Publikováno v:
Pharmaceutical Chemistry Journal.
The bioequivalence of the tablet dosage form of RU-31 substance was studied. The main pharmacokinetic parameters were determined. The actual relative bioequivalence index was calculated and turned out to be ~100%. RU-31 from tablets did not accumulat
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::7582a3b10f0e866b25fe4b7921a6e8be
https://doi.org/10.1007/s11094-021-02421-0
https://doi.org/10.1007/s11094-021-02421-0
Autor:
V. N. Perfilova, Ivan N. Tyurenkov, A. F. Ryabukha, O. S. Vasil’eva, L. A. Smirnova, L. M. Ganicheva, K. A. Kuznetsov, M. V. Velikopol’skaya
Publikováno v:
Pharmaceutical Chemistry Journal. 53:1090-1092
An HPLC method for quantitative determination of the new biologically active GABA derivative Solifen was developed. The method sensitivity, compound retention time and UV absorption maximum were determined. The optimum extractant for the compound fro
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::bdc6edbf0eb5bef4261f81b84a744d1a
https://doi.org/10.1007/s11094-020-02128-8
https://doi.org/10.1007/s11094-020-02128-8
Autor:
E. A. Suchkov, K. A. Kuznetsov, M. V. Velikopol’skaya, A. F. Ryabukha, D. A. Bakulin, Ivan N. Tyurenkov, L. A. Smirnova, É. F. Stepanova, A. M. Shevchenko
Publikováno v:
Pharmaceutical Chemistry Journal. 52:495-496
The bioequivalence of mefebut drug substance and its tablet dosage form was investigated by studying the main pharmacokinetic parameters and calculating the relative bioavailability. The results showed that mefebut circulated for up to 4 h in rabbit
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::a9335352e3baec3c6b83cbf6d5bb04cc
https://doi.org/10.1007/s11094-018-1846-x
https://doi.org/10.1007/s11094-018-1846-x