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UV Method Development and Validation of Eperisone Hydrochloride in Bulk and Tablet Formulation.
Author(s):
1. Saima Saleem: Faculty of Pharmacy, Jinnah University for Women, Karachi, Pakistan
2. Saeeda Bano: Plattinum Pharmaceuticals (Pvt.) Ltd, Karachi, Pakistan
3. Safila Naveed: Faculty of Pharmacy, Jinnah University for Women, Karachi, Pakistan
4. M Tanweer Alam: Faculty of Pharmacy, Jinnah University for Women, Karachi, Pakistan
5. Amanullah Khan: Drugs Testing Laboratory Quetta, Health Department Baluchistan, Quetta, Pakistan
6. Ghulam Sarwer: Faculty of Pharmacy, Jinnah University for Women, Karachi, Pakistan
7. Huma Dilshad: Faculty of Pharmacy, Jinnah University for Women, Karachi, Pakistan
Abstract:
Objective: To develop and validate a UV simple, precise and cost saving method for fast analysis of eperisone hydrochloride in eperisone tablets. Method: The test is developed by using methanol as diluent, performed on UV visible double beam spectrophotometer at range of 200nm-400nm, and found absorbance on maximum wavelength of 260 nm. The test is then validated by using complete parameters of method validation i.e., linearity, precision, selectivity, accuracy, repeatability, robustness, limit of quantitation and detection. The complete procedure is carried out as per United State Results: Calculate individually all parameters of method validation as per standard that should meet the validation criteria. Conclusion: As per above discussion the method is precise and accurate for analysis of eperisone hydrochloride in eperisone hydrochloride tablets.
Page(s): 39-43
DOI: DOI not available
Published: Journal: RADS Journal of Pharmacy & Pharmaceutical Sciences, Volume: 5, Issue: 4, Year: 2017
Keywords:
UV Spectrophotometer , eperisone hydrochloride
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