Zobrazeno 1 - 4
of 4
pro vyhledávání: '"Yu. E. Boldina"'
Publikováno v:
Разработка и регистрация лекарственных средств, Vol 0, Iss 1, Pp 100-104 (2019)
Validation of UV-spectrometry assay method for dissolution profile test for levofloxacine tablets was carried out. The evaluated validation characteristics were: specificity, linearity, accuracy, precision, analytical range. It was shown than main va
Externí odkaz:
https://doaj.org/article/66f7b35d1943432faf3e5b87732c8748
Publikováno v:
Разработка и регистрация лекарственных средств, Vol 0, Iss 2, Pp 94-97 (2019)
Validation of UV-spectrometry assay method for dissolution profile test for levofloxacine tablets was carried out. The evaluated validation characteristics were: specificity, linearity, accuracy, precision, and analytical range. It was shown than mai
Externí odkaz:
https://doaj.org/article/adfce49255ef410b9b9521c46fa6c9d6
Autor:
T. N. Komarov, Yu. V. Medvedev, I. E. Shohin, Yu. E. Boldina, A. A. Lvova, E. S. Melnikov, E. N. Fisher, R. V. Ivanov, R. J. Maksvitis
Publikováno v:
Разработка и регистрация лекарственных средств, Vol 0, Iss 3, Pp 174-179 (2019)
A new method for determination of moxifloxacin in human plasma using HPLC with UV-detection is described. The sample preparation was made by protein precipitation by 50% trifluoracetic acid solution. The method was validated in terms of selectivity,
Externí odkaz:
https://doaj.org/article/2c12f4c9ec2e4e6daa389810a5935d3a
Publikováno v:
Разработка и регистрация лекарственных средств, Vol 0, Iss 3, Pp 158-161 (2019)
Dissolution profile study for extended-release valproic acid preparations was performed in three dissolution media: 0.1 M hydrochloric acid, acetate buffer pH 4.5, citrate-phosphate buffer pH 6.8 using Apparatus 1 at 75 rpm. Time points were 1, 2, 3,
Externí odkaz:
https://doaj.org/article/d6177ed85fb344f885a63a4be74dd156