VALIDATION OF UV-SPECTROMETRY ASSAY METHOD FOR DISSOLUTION PROFILE TEST FOR LEVOFLOXACINE TABLETS

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 validation characteristics meet the Russian State Ph...

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Main Authors: A. A. Lvova, I. E. Shohin, L. A. Menshikova, T. N. Komarov, Yu. E. Boldina, Yu. V. Medvedev
Format: Article
Language:Russian
Published: LLC Center of Pharmaceutical Analytics (LLC «CPHA») 2019-01-01
Series:Разработка и регистрация лекарственных средств
Subjects:
Online Access:https://www.pharmjournal.ru/jour/article/view/228
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author A. A. Lvova
I. E. Shohin
L. A. Menshikova
T. N. Komarov
Yu. E. Boldina
Yu. V. Medvedev
author_facet A. A. Lvova
I. E. Shohin
L. A. Menshikova
T. N. Komarov
Yu. E. Boldina
Yu. V. Medvedev
author_sort A. A. Lvova
collection DOAJ
description 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 validation characteristics meet the Russian State Pharmacopoeia requirements.
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last_indexed 2024-04-10T01:41:22Z
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spelling doaj.art-66f7b35d1943432faf3e5b87732c87482023-03-13T09:13:57ZrusLLC Center of Pharmaceutical Analytics (LLC «CPHA»)Разработка и регистрация лекарственных средств2305-20662658-50492019-01-0101100104228VALIDATION OF UV-SPECTROMETRY ASSAY METHOD FOR DISSOLUTION PROFILE TEST FOR LEVOFLOXACINE TABLETSA. A. Lvova0I. E. Shohin1L. A. Menshikova2T. N. Komarov3Yu. E. Boldina4Yu. V. Medvedev5ФГБУН НЦБМТ ФМБА РоссииФГБУН НЦБМТ ФМБА РоссииФГБУН НЦБМТ ФМБА РоссииФГБУН НЦБМТ ФМБА РоссииФГБУН НЦБМТ ФМБА РоссииГБОУ ВПО Первый МГМУ им. И.М. Сеченова Минздрава РоссииValidation 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 validation characteristics meet the Russian State Pharmacopoeia requirements.https://www.pharmjournal.ru/jour/article/view/228валидациялевофлоксацинуф-спектрофотометриятест кинетики растворения
spellingShingle A. A. Lvova
I. E. Shohin
L. A. Menshikova
T. N. Komarov
Yu. E. Boldina
Yu. V. Medvedev
VALIDATION OF UV-SPECTROMETRY ASSAY METHOD FOR DISSOLUTION PROFILE TEST FOR LEVOFLOXACINE TABLETS
Разработка и регистрация лекарственных средств
валидация
левофлоксацин
уф-спектрофотометрия
тест кинетики растворения
title VALIDATION OF UV-SPECTROMETRY ASSAY METHOD FOR DISSOLUTION PROFILE TEST FOR LEVOFLOXACINE TABLETS
title_full VALIDATION OF UV-SPECTROMETRY ASSAY METHOD FOR DISSOLUTION PROFILE TEST FOR LEVOFLOXACINE TABLETS
title_fullStr VALIDATION OF UV-SPECTROMETRY ASSAY METHOD FOR DISSOLUTION PROFILE TEST FOR LEVOFLOXACINE TABLETS
title_full_unstemmed VALIDATION OF UV-SPECTROMETRY ASSAY METHOD FOR DISSOLUTION PROFILE TEST FOR LEVOFLOXACINE TABLETS
title_short VALIDATION OF UV-SPECTROMETRY ASSAY METHOD FOR DISSOLUTION PROFILE TEST FOR LEVOFLOXACINE TABLETS
title_sort validation of uv spectrometry assay method for dissolution profile test for levofloxacine tablets
topic валидация
левофлоксацин
уф-спектрофотометрия
тест кинетики растворения
url https://www.pharmjournal.ru/jour/article/view/228
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