Fosinopril-sodium and its degradation product analysis in Monopril® tablets
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The reversed-phase high-performance liquid chromatographic (RP-HPLC) method has been developed for the simultaneous determination of fosinopril-sodium and its degradation product in Monopril® tablets. The chromatographic system Hewlett Packard 1100 consisted era HP 1100 pump, HP 1100 UV-VIS detector and HP ChemStation integrator. Separations were performed on the X Terra™ 150 mm x 4.6 mm, 5 μm particle column at 45 °C. The samples were introduced through a Rheodyne injector valve with a 20 μL sample loop. Methanol-water (75:25 V/V) was used as a mobile phase, with flow rate 1 mL/min. pH was adjusted to 3.1 with ortophosphoric acid. UV detection was performed at 220 nm. Propylparaben was used as an internal standard. The results obtained showed a good agreement with the declared contents. Recovery values for fosinoprit-sodium were from 101.6% to 102.9%. Content of degradation product SQ 27519 was lower than 5%. The proposed method is rapid, accurate, selective and because of its sensiti...vity and reproducibility, it may be used for the quantitative analysis of fosinopril-sodium and its degradation product in Monopril® tablets.
Keywords:Degradation product / Fosinopril-sodium / RP-HPLC
Source:Acta Chimica Slovenica, 2003, 50, 2, 327-333
- Slovensko Kemijsko Drustvo