Author:
Bhalme V. M.,Jumade P. P.,Bawankar Ram D,Wanjari D. S.,Mundhada D. R.
Abstract
Objective: Method development, validation & stability indicating studies for simultaneous estimation of Anti-Hypertensive drugs, Benidepine (BEN) and Metoprolol (MET) from pharmaceutical formulation by RP-HPLC.
Methods: For present work, reverse phase chromatography was selected as its suggested use for ionic and moderate to non-polar compounds. Reverse phase chromatography is simple, suitable, better regarding efficiency, stability, and reproducibility. C18 packed column, a 100 X 2.1mm. ID column of 5.0 μm particle packing, was selected for separation of BEN and MET. Different solvent systems were tried and optimized in combinations as mobile phase. BEN (4 μg/ml) and MET (50 μg/ml) in 15mM ammonium formate-Methanol (15:85 v/v) was developed as it was showing good peak shapes and a significant amount of resolution. The mobile phase was flowed at 1.2 ml/min with detection of BEN analytes at 236 nm and MET analytes at 225 nm respectively.
Result: Method development was done. Specificity, linearity, accuracy, precision, robustness, limit of detection and limit of quantitation were used to accomplish validation. The method was found linear from 32.5 – 500 µg.ml-1 for both BEN and MET individually. The percentage recovery of BEN when placed for period of 12 hours was found to 100% in 0.1N/M NaOH at 60˚C and Thermal (60˚C); 12 % degradation in 0.1N/M HCl at 60˚C; Oxidation (3-6% H2O2) at room temperature whereas for MET was 100 % in 0.1N/M NaOH, 0.1N/M HCl at 60˚C, at thermal (60˚C) as well as oxidation by 3-6% H2O2 at room temperature.
Conclusion: Developed analytical method for the simultaneous estimation of Benidipine (BED) and Metoprolol (MET) in both bulk and tablet formulation has obliged the ICH guidelines including, tailing factor (T), separation factors (α), theoretical plates (N), capacity factor (k’), resolution (R) and RSD (%). The validated stress degradation studies under thermal, oxidative, alkali and acid ascertained few degradation products for Benidipine whereas the Metoprolol was unaffected with forced degradation studies.
Keywords: Benidipine, Metoprolol, Reverse-Phase High Performance Liquid Chromatography, Stability indicating method.
Publisher
Society of Pharmaceutical Tecnocrats
Reference27 articles.
1. 1. Rao, RN., Nagaraju, V. An overview of the recent trends in development of HPLC methods for determination of impurities in drugs Journal of Pharmaceutical and Biomedical Analysis, 2003; 33:335-377.
2. 2. Nadella NP., Ratnakaram VN., Srinivasu N. Development and validation of UPLC method for simultaneous quantification of carvedilol and ivabradine in the presence of degradation products using DoE concept, Journal Of Liquid Chromatography & Related Technologies, 2018; 3:1-9.
3. 3. Patel JM., et al, Method Development and Validation for Simultaneous Estimation of Benidipine Hydrochloride and Metoprolol Succinate in Tablet, Journal of Drug Delivery & Therapeutics, 2019; 9:28-33.
4. 4. Gopika VC, and Remi SL., Validated UV Spectrophotometric Method for Simultaneous Estimation of Metoprolol Succinate and Benidipine Hydrochloride in their Combined Tablet Dosage Form, Asian Journal of Pharmaceutical and Health Sciences, 2018; 8:1968-1975.
5. 5. Drug Profile for Benidipine HCl, August-2017. Available from: http:// www.drugbank.ca/drugs/DB09231. [Last accessed on 2017 Nov 20].
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