Konu "Tablet Analysis" için Eczacılık Fakültesi listeleme
Toplam kayıt 6, listelenen: 1-6
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The determination of bupropion hydrochloride in pharmaceutical dosage forms by original UV- and second derivative UV spectrophotometry, potentiometric and conductometric methods [Bupropion Hidroklorür'un Orjinal UV- ve 2. Tiirev UV Spektrofotometri, Potansiyotnetri ve Kondüktotnetri Yöntemleri He Farmasötik Dozqj Formlanndaki Tayini]
(2010)Spectrophotometric, potentiometric and conductometric methods are developed for the determination of bupropion hydrochloride (BUP) in pharmaceutical tablets. For the first method, original UV-spectrophotometry, 252 nm was ... -
Determination of carbamazapine by flow-injection analysis: Its application to tablet analysis and dissolution studies
(Taylor & Francis Inc, 2006)Flow injection analysis (FIA) of carbamazepine (CBZ) and its relevant application to the conventional CBZ tablets, e. g., content uniformity test and tablet dissolution, is described in this study. An aqueous solution of ... -
Determination of leflunomide in tablets by high performance liquid chromatography
(Elsevier Science BV, 2006)In the present study, a reverse phase high performance liquid chromatography (HPLC) method was validated and applied for the determination of leflunomide in tablets. Chromatographic separation of leflunomide and oxazepam ... -
Development of a validated high-performance liquid chromatographic method for the determination of Lurasidone in pharmaceuticals
(Marmara University, Fac Pharmacy, 2017)A new, rapid and simple HPLC method for determination of Lurasidone in its tablets has been developed and validated. Lurasidone and internal standard (Chlorpromazine) was separated on a Zorbax XDB C8 column (4.6 x 50 mm, ... -
A Stability Indicating Ion-Pair Lc Method for the Determination of Asenapine in Pharmaceuticals
(Soc Chilena Quimica, 2017)In this study, a new, simple and specific stability indicating ion-pair LC method was developed and fully validated for the determination of asenapine in tablets. The analysis was performed on an Agilent Eclipse XDB-C8 ... -
A Validated Thin-Layer Chromatographic Method for Analysis of Bupropion Hydrochloride in a Pharmaceutical Dosage Form
(Akademiai Kiado Zrt, 2010)A simple and sensitive thin-layer chromatographic method has been established for analysis of bupropion hydrochloride in pharmaceutical tablets. Chromatography on silica gel 60 F-254 plates with 30:10:1 (v/v) ethanol ...