Validation of assay method of nifedipine in tablets by liquid chromatography

L. S. Lohoyda

Abstract


The aim of this study was the validation of methods of quantitative determination of nifedipine in  tablets by liquid chromatography. The chromatographic analysis was performed on nifedipine liquid chromatograph Agilent 1290 Infinity II LC System. A validation of methods of quantitative determination of nifedipine by high performance liquid chromatography tablets was performed. It was established that the method proves the requirements of the State Pharmacopoeia of Ukraine for the main validation parameters: specificity, accuracy, linearity, robasnist. The results obtained in this study clearly indicate that the developed HPLC method is fast, economical, simple, accurate and suitable for determination of nifedipine in medicines.


Keywords


nifedipine; quantitative analysis; validation; chromatography; validation parameters.

References


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DOI: http://dx.doi.org/10.11603/mcch.2410-681X.2016.v0.i4.7267

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