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Toplam kayıt 4, listelenen: 1-4
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 ...
An LC Method for the Determination of Bupropion and Its Main Metabolite, Hydroxybupropion in Human Plasma
(Springer Heidelberg, 2009)
A new LC method has been developed and validated for the direct determination of bupropion and its main metabolite, hydroxybupropion in human plasma. Plasma samples were analyzed after a simple, one step protein precipitation ...
Determination of piribedil in human serum, urine and pharmaceutical dosage form by LC-DAD
(Springer Heidelberg, 2008)
A rapid, selective and sensitive reversed-phase liquid chromatographic (LC) method was developed for the determination of piribedil in human serum, urine and pharmaceutical dosage form. LC analysis was carried out using ...
A validated HPLC method with fluorescence detection for the determination of droperidol in pharmaceutical tablets, human serum, and human milk
(Springer Heidelberg, 2007)
A sensitive and simple HPLC method with fluorimetric detection has been developed for determination of droperidol in pharmaceutical tablets, human serum, and human milk. Chromatography was performed on a 100 mm x 3 mm i.d. ...