Konu "Method Validation" için Makale Koleksiyonu listeleme
Toplam kayıt 4, listelenen: 1-4
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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 ... -
Development and validation of a simple and efficient HPLC method for the determination of zonisamide in pharmaceuticals and human plasma
(Maik Nauka/Interperiodica/Springer, 2013)A simple and efficient liquid chromatographic method has been developed and validated for the determination of zonisamide in pharmaceuticals and human plasma. Plasma samples are analyzed after one step protein precipitation ... -
Retention Behaviour of Bupropion Hydrochloride in Reversed Phase Ion Pair LC and Validated Analysis of the Drug in Pharmaceuticals
(Springer Heidelberg, 2010)The chromatographic behaviour of bupropion hydrochloride, a basic drug of pK (a) 7.9, has been investigated under reversed-phase ion-pairing conditions and the results were used to develop a method for analysis of bupropion ... -
A Simple and Specific Hplc Method for the Determination of Atomoxetine in Pharmaceuticals and Human Plasma
(Taylor & Francis Inc, 2010)A liquid chromatographic method has been described for the determination of atomoxetine in pharmaceuticals and human plasma. Plasma samples were analyzed after a simple, one step protein precipitation with methanol, and ...