Research Article
Determination of Magnesium Valproate and Its Process Related Impurities by Ultraperformance Liquid Chromatography
Table 1
Chromatographic conditions of proposed analytical method.
| Parameters | Optimum condition |
| Mobile phase A | 5 mM ammonium dihydrogen orthophosphate (PH = 3.0) | Mobile phase B | acetonitrile (HPLC grade) | Column | Acquity BEH C18 (100 mm 2.1 mm i.d., 1.7 particle size) | Flow rate | 0.3 mL/min | Isocratic elution at | 55 : 45, v/v | Detection | 215 nm UV | Diluent | Acetonitrile : water (1 : 1) | Injection volume | 5 L |
|
|