Original ArticleInternational Journal of Pharmaceutical InvestigationVol. 12 | Issue 3 | 2022 | pp. 288–292Open access
Development and Validation of Prochlorperazine Maleate in Bulk and Pharmaceutical Dosage Form by UV Spectroscopic Method
- 1*,
- 1,
- 1
- 1 Department of Pharmaceutical Chemistry, A.R. College of Pharmacy and G. H Patel Institute of Pharmacy Vallabh Vidyanagar, Anand, Gujarat, INDIA.
Published in International Journal of Pharmaceutical Investigation
Correspondence: Hina Bagada
Department of Pharmaceutical Chemistry, A.R. College of Pharmacy and G. H Patel Institute of Pharmacy Vallabh Vidyanagar, Anand, Gujarat, INDIA.
Email: bagadahina@gmail.com
Copyright: © 2022 Manuscript Technomedia. This is an open access article.
- Published:
- Jul 27, 2022
- Received:
- May 6, 2022
- Accepted:
- Jun 6, 2022
How to cite
Bagada, H., Bhut, V., & Parmar, H. (2022). Development and Validation of Prochlorperazine Maleate in Bulk and Pharmaceutical Dosage Form by UV Spectroscopic Method. International Journal of Pharmaceutical Investigation, 12(3), 288–292. https://doi.org/10.5530/ijpi.2022.3.50
Abstract
Background: Prochlorperazine maleate is an antipsychotic and antiemetic drug that is available as tablets on the market for oral administration. The main object of this research work is to develop and validate the easiest UV spectroscopic method for the determination of Prochlorperazine maleate for tablet formulation (marketed formulation). Materials and Methods: A simple, reproducible and efficient method for the determination of Prochlorperazine maleate in bulk and tablet formulations have been developed. The developed method is based on the estimation by UVVisible spectroscopy. In this method, 0.3M HCL was selected as the solvent. A Wavelength selected for estimation of Prochlorperazine maleate was 254 nm. Results: Linearity was found in the concentration range 2-16μg/ml (R2=0.9909). A recovery study was found to be 98.01-99.79% for Prochlorperazine maleate. The method was found to be precise as % RSD was low in repeatability, intermediate precision, and reproducibility. LOD and LOQ were found to be 0.58 and 1.75 respectively. Conclusion: The method was found to be very simple, and precise. It also had a good recovery. The Developed method can be used for further routine analysis and stability study of a Prochlorperazine maleate.
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Article metadata
| Title | Development and Validation of Prochlorperazine Maleate in Bulk and Pharmaceutical Dosage Form by UV Spectroscopic Method |
|---|---|
| Authors | Hina Bagada; Vishva Bhut; Himaxi Parmar |
| Affiliations | Department of Pharmaceutical Chemistry, A.R. College of Pharmacy and G. H Patel Institute of Pharmacy Vallabh Vidyanagar, Anand, Gujarat, INDIA. |
| Corresponding author | bagadahina@gmail.com |
| Journal | International Journal of Pharmaceutical Investigation |
| Volume / Issue | Vol. 12, Issue 3 (2022) |
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