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. 2013 Apr-Jun;81(2):437-8.
doi: 10.3797/scipharm.1209-12. Epub 2012 Nov 19.

A Single Gradient Stability-Indicating Reversed-Phase LC Method for the Estimation of Impurities in Omeprazole and Domperidone Capsules

Affiliations

A Single Gradient Stability-Indicating Reversed-Phase LC Method for the Estimation of Impurities in Omeprazole and Domperidone Capsules

Raja Kumar Seshadri et al. Sci Pharm. 2013 Apr-Jun.

Abstract

A gradient reversed-phase liquid chromatographic (RP-LC) method was developed for the quantitative estimation of impurities in the pharmaceutical dosage form of Omeprazole and Domperidone capsules. The developed method is a stability-indicating test method for the estimation of impurities generated during the formulation and storage of Omeprazole and Domperidone capsules. The chromatographic separation was achieved on a column packed with octadecyl silane, having a column length of 250 mm and diameter of 4.6 mm with a particle size of 5 μm, and by following a gradient program using a combination of a monobasic potassium phosphate buffer (0.05M) and acetonitrile. Since the spectral properties were similar, both compounds' individual impurities were estimated at 285 nm. Forced degradation studies were performed on Omeprazole pellets (enteric coated) and Domperidone pellets (SR coated) encapsulated in size '1' hard gelatin capsules. Omeprazole and Domperidone were degraded using acid hydrolysis (0.1 N hydrochloric acid), base (0.1 N sodium hydroxide), oxidation (50% hydrogen peroxide), heat (105 °C), and UV light (254 nm). The established method was validated and found to be linear, accurate, precise, specific, robust, and rugged.

Keywords: Domperidone; Forced Degradation; Method validation; Omeprazole; RP-LC.

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Figures

Fig. 1
Fig. 1
Chemical structures of OM and DP
Fig. 2
Fig. 2
Chemical structures of impurities
Fig. 2
Fig. 2
Chemical structures of impurities
Fig. 3
Fig. 3
The typical chromatogram of Diluent
Fig. 4
Fig. 4
The typical chromatogram of Standard
Fig. 5
Fig. 5
The typical chromatogram of Test preparation with spiked impurities
Fig. 6
Fig. 6
The typical chromatogram of Placebo
Fig. 7
Fig. 7
The typical Chromatogram of Sample in 1 M NaOH
Fig. 7a
Fig. 7a
Purity Plot of Omeprazole in 1M NaOH
Fig. 7b
Fig. 7b
Purity Plot of Domperidone in 1M NaOH
Fig. 8
Fig. 8
The typical Chromatogram of Sample in 1 M HCl
Fig. 8a
Fig. 8a
Purity Plot of Omeprazole in 1M HCl
Fig. 8b
Fig. 8b
Purity Plot of Domperidone in 1M HCl
Fig. 9
Fig. 9
The typical Chromatogram of Sample in 50% H2O2
Fig. 9a
Fig. 9a
Purity Plot of Omeprazole in 50% H2O2
Fig. 9b
Fig. 9b
Purity Plot of Domperidone in 50% H2O2
Fig. 10
Fig. 10
The typical Chromatogram of Sample in Heat
Fig. 10a
Fig. 10a
Purity Plot of Omeprazole in Heat
Fig. 10b
Fig. 10b
Purity Plot of Domperidone in Heat
Fig. 11
Fig. 11
The typical Chromatogram of Sample in UV
Fig. 11a
Fig. 11a
Purity Plot of Omeprazole in UV
Fig. 11b
Fig. 11b
Purity Plot of Domperidone in UV
Fig. 12
Fig. 12
Linearity plot of Omeprazole C 789
Fig. 13
Fig. 13
Linearity plot of Omeprazole N Oxide
Fig. 14
Fig. 14
Linearity plot of Omeprazole Desmethoxy impurity
Fig. 15
Fig. 15
Linearity plot of Omeprazole Sulphone
Fig. 16
Fig. 16
Linearity plot of Omeprazole Sulphide
Fig. 17
Fig. 17
Linearity plot of Domperidone Imp-A
Fig. 18
Fig. 18
Linearity plot of Domperidone Imp-B
Fig. 19
Fig. 19
Linearity plot of Domperidone Imp-C
Fig. 20
Fig. 20
Linearity plot of Domperidone Imp-D
Fig. 21
Fig. 21
Linearity plot of Domperidone Imp-F

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