Analytical Method Development and Validation of Prucalopride Succinate in Bulk and Formulation by UV-Visible Spectrophotometry

Purpose: Analytical method development and validation for the quantitative determination of Prucalopride succinate in bulk and tablet formulation which plays major role in the development and manufacture of pharmaceuticals. Methods: In the present work a simple, rapid and reproducible UV-Visible Spe...

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Bibliographic Details
Published in:Research journal of pharmacy and technology 2021-08, Vol.14 (8), p.4189-4191
Main Authors: Bhosale, A.C., Bhagat, V.C., Kunjir, V. V, Kardile, D.P., Shete, R.V.
Format: Article
Language:English
Subjects:
Accuracy
Drug dosages
Pharmaceutical sciences
Pharmacy
Quality control
Spectrum analysis
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Summary:Purpose: Analytical method development and validation for the quantitative determination of Prucalopride succinate in bulk and tablet formulation which plays major role in the development and manufacture of pharmaceuticals. Methods: In the present work a simple, rapid and reproducible UV-Visible Spectrophotometric method was developed and validated according to ICH guidelines. Results and Conclusions: The parameters linearity, specificity, precision, accuracy, and robustness were studied. The wavelength 243nm was selected for the estimation of drug using methanol as a solvent. The drug obeys Beer-lambert’s law over the concentration range 2-10μg/ml. The accuracy of the method was assessed by recovery studies and was found between 97.2- 98.3 %. The method was successfully applied for routine analysis of Prucalopride succinate in bulk and formulation.
ISSN:0974-3618
0974-360X
0974-306X
DOI:10.52711/0974-360X.2021.00725