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DISSOLUTION PROFILE STUDY FOR EXTENDED RELEASE VALPROIC ACID DOSAGE FORM (DEPAKINE® CHRONO)

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, 4, and 6 hours. Assay of released API was perform...

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Hlavní autoři: A. A. Lvova, Yu. E. Boldina, I. E. Shohin, T. N. Komarov, L. A. Menshikova, Yu. V. Medvedev
Médium: Artigo
Jazyk:Russo
Vydáno: LLC Center of Pharmaceutical Analytics (LLC «CPHA») 2019-01-01
Edice:Разработка и регистрация лекарственных средств
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On-line přístup:https://www.pharmjournal.ru/jour/article/view/303
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