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

L. A. Menshikova, A. A. Lvova,I. E. Shohin,Yu. E. Boldina,T. N. Komarov,Yu. V. Medvedev

Разработка и регистрация лекарственных средств（2019）

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摘要

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 main validation characteristics meet the Russian State Pharmacopoeia XIII requirements.

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关键词

moxifloxacine,validation,uv-spectrophotometry,dissolution profile test

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