Zobrazeno 1 - 10
of 20
pro vyhledávání: '"T. B. Shemeryankina"'
Autor:
O. V. Evdokimova, A. V. Beketova, O. A. Naumova, I. V. Klinkova, T. B. Shemeryankina, L. A. Ladygina, K. S. Bushchik
Publikováno v:
Регуляторные исследования и экспертиза лекарственных средств, Vol 13, Iss 4, Pp 567-577 (2023)
Scientific relevance. Cardiac glycosides have been used in medicine for over two centuries. Current studies suggest that biologically active substances from this group can be used to treat not only heart conditions but also viral infections, cancers,
Externí odkaz:
https://doaj.org/article/1f1b15f8869942cfa799d645797bd924
Autor:
A. S. Alekseeva, M. V. Gavrilin, T. B. Shemeryankina, M. S. Smirnova, E. P. Fedorova, T. M. Kargina, O. O. Novikov, S. A. Kovaleva, N. N. Boyko
Publikováno v:
Регуляторные исследования и экспертиза лекарственных средств, Vol 11, Iss 3, Pp 185-192 (2021)
A great variety of components in multivitamin preparations containing folic acid, and a variety of test methods and conditions of folic acid determination proposed by manufacturers, require alignment of test procedures for products with similar compo
Externí odkaz:
https://doaj.org/article/54e5c6c4b5fc425aab2ffd80d603b36a
Autor:
A. S. Alekseeva, T. B. Shemeryankina, M. N. Lyakina, M. S. Smirnova, E. P. Fedorova, S. D. Kakhramanova
Publikováno v:
Регуляторные исследования и экспертиза лекарственных средств, Vol 11, Iss 3, Pp 174-184 (2021)
Vitamin A is present in multivitamin products mainly in the form of retinol esters: retinyl acetate, retinyl palmitate, and beta carotene—retinol precursor (dimer) found in plants, which is capable of converting into retinol in liver cells. Retinol
Externí odkaz:
https://doaj.org/article/cacada5572a349568ddb5cb70a6c9a15
Publikováno v:
Антибиотики и Химиотерапия, Vol 62, Iss 5-6, Pp 63-67 (2020)
The present article reviews the modern approaches for the standardization of synthetic pharmaceutical substances that are realized in the form of national pharmacopoeial standards - monographs published in State Pharmacopoeia of Russian Federation. T
Externí odkaz:
https://doaj.org/article/65de55d08fe14ce08e4ac25029a2fc1d
Autor:
E. I. Sakanyan, N. D. Bunyatyan, M. N. Lyakina, N. S. Tereshina, T. B. Shemeryankina, N. A. Postoyuk
Publikováno v:
Регуляторные исследования и экспертиза лекарственных средств, Vol 0, Iss 2, Pp 60-63 (2018)
RETRACTED ARTICLEThe research related to the development of general monographs regulating the requirements for dosage forms used in homeopathic practice is of current interest. The need to harmonize the requirements for the mentioned dosage forms in
Externí odkaz:
https://doaj.org/article/cb7849f4ed294a018f819d6310803b47
Publikováno v:
Регуляторные исследования и экспертиза лекарственных средств, Vol 0, Iss 2, Pp 54-58 (2018)
The State Pharmacopoeia of the Russian Federation is a collection of general monographs and pharmacopoeial monographs. It should be reissued at least once in 5 years. The next scheduled edition of the State Pharmacopoeia of the Russian Federation is
Externí odkaz:
https://doaj.org/article/c315c6e265204bfd9d97118a82e5cf8b
Publikováno v:
Регуляторные исследования и экспертиза лекарственных средств, Vol 0, Iss 1, Pp 35-39 (2018)
For the purpose of prevention and treatment of various diseases, herbal medicinal products are used along with a wide range of small molecule drugs. Herewith herbal preparations are not only herbs and combined herbal products, but also various galeni
Externí odkaz:
https://doaj.org/article/f6d81af7ed2444f99c51d14ba0d32d4c
Publikováno v:
Pharmaceutical Chemistry Journal. 52:873-877
Experimental validation of methods and procedures featured in draft general pharmacopoeial and pharmacopoeial monographs is an important task for Russian compendial science and practice. These studies provide a basis for adopting state compendial dru
Autor:
Yu. V. Olefir, T. B. Shemeryankina, S. A. Zaitsev, A. V. Barmin, E. I. Sakanyan, S. P. Senchenko
Publikováno v:
Pharmaceutical Chemistry Journal. 52:744-748
The current classification of impurities in chemical and mineral drug substances is presented. General approaches to standardization of chemical and mineral drug substances according to the Purity section are given depending on their origin and produ
Publikováno v:
Pharmaceutical Chemistry Journal. 51:731-734
Issues related to regulation of the quality of compounded medicinal preparations by the State Pharmacopoeia of the Russian Federation are considered. Topical questions of the development and implementation of both general clauses and particular monog