Author(s):
Ganesh Sonawane, Kiran Gangurde, Vijayraj Sonawane, Chandrashekhar Patil, Rushikesh Bachhav, Mayur Bhamare, Kajal Pansare, Deepak Sonawane, Sunil Mahajan
Email(s):
gbsonawane8@gmail.com
DOI:
10.52711/0974-4150.2025.00011
Address:
Ganesh Sonawane*, Kiran Gangurde, Vijayraj Sonawane, Chandrashekhar Patil, Rushikesh Bachhav, Mayur Bhamare, Kajal Pansare, Deepak Sonawane, Sunil Mahajan
Divine College of Pharmacy, Satana, Nashik - 423301 (India).
*Corresponding Author
Published In:
Volume - 18,
Issue - 2,
Year - 2025
ABSTRACT:
A simple, accurate, and precise UV-Visible spectrophotometric method for the quantification of Amlodipine Besylate in pharmaceutical formulations was developed and validated in accordance with ICH Q2(R1) guidelines. The method involved the preparation of standard solutions in the concentration range of 2–10 µg/mL, with absorbance measured at the ?max of 239 nm. The method demonstrated excellent linearity with a regression coefficient (R²) of 0.9995. Recovery studies at 80%, 100%, and 120% levels showed high accuracy, with mean recoveries ranging from 99.79% to 100.33%, confirming its reliability. Precision was evaluated through intra-day and inter-day studies, yielding %RSD values of 0.84% and 0.79%, respectively, indicating excellent repeatability. The method also showed high specificity, with no interference from excipients, and sensitivity with a LOD of 0.096 µg/mL and LOQ of 0.291 µg/mL. Robustness testing demonstrated minimal variation with small changes in experimental conditions. The method was successfully applied to the analysis of Amlodipine Besylate tablets, yielding an assay of 99.87% of the labeled content, which is within the acceptable range. The developed method is a reliable, cost-effective tool for routine quality control in the pharmaceutical industry for the analysis of Amlodipine Besylate in both raw materials and finished formulations.
Cite this article:
Ganesh Sonawane, Kiran Gangurde, Vijayraj Sonawane, Chandrashekhar Patil, Rushikesh Bachhav, Mayur Bhamare, Kajal Pansare, Deepak Sonawane, Sunil Mahajan. Analytical Method Development and Validation of Amlodipine Besylate by UV-Visible Spectroscopy. Asian Journal of Research in Chemistry.2025; 18(2):71-6. doi: 10.52711/0974-4150.2025.00011
Cite(Electronic):
Ganesh Sonawane, Kiran Gangurde, Vijayraj Sonawane, Chandrashekhar Patil, Rushikesh Bachhav, Mayur Bhamare, Kajal Pansare, Deepak Sonawane, Sunil Mahajan. Analytical Method Development and Validation of Amlodipine Besylate by UV-Visible Spectroscopy. Asian Journal of Research in Chemistry.2025; 18(2):71-6. doi: 10.52711/0974-4150.2025.00011 Available on: https://ajrconline.org/AbstractView.aspx?PID=2025-18-2-2
REFERENCES:
1. Ferri, C., and Grassi, G. Amlodipine: A pharmacological and clinical review. Journal of Hypertension. 2010; 28(3): 46-54.
2. Triggle, D. J. Calcium channel blockers: Mechanisms of action, vascular selectivities, and clinical relevance. Cleveland Clinic Journal of Medicine. 2003; 70(9): 793-803.
3. Skoog, D. A., Holler, F. J., and Crouch, S. R. Principles of Instrumental Analysis. 7th ed. Cengage Learning. 2017
4. Gaikwad, N., and Jadhav, R. A review on UV spectroscopy in pharmaceutical analysis. Asian Journal of Pharmaceutical Analysis. 2022; 12(2): 95-102.
5. International Council for Harmonisation (ICH). Validation of Analytical Procedures: Text and Methodology Q2(R1). 2005
6. Patel, M., and Patel, N. UV-visible spectrophotometric methods for pharmaceuticals. Asian Journal of Pharmaceutical Research and Development. 2019; 7(3): 45-50.
7. Shimadzu Corporation. UV-1800 UV-Visible Spectrophotometer Specifications. 2020
8. Beckett, A. H., and Stenlake, J. B. Practical Pharmaceutical Chemistry. 4th ed. CBS Publishers. 2007
9. Skoog, D. A., Holler, F. J., and Crouch, S. R. Principles of Instrumental Analysis. 7th ed. Cengage Learning. 2017
10. International Council for Harmonisation (ICH). Validation of Analytical Procedures: Text and Methodology Q2(R1). 2005
11. Sharma, B. K. Instrumental Methods of Chemical Analysis. Goel Publishing House. 2000
12. Rao, P., and Gupta, R. Validation studies on spectrophotometric analysis. Journal of Analytical Science. 2018; 5(1): 23-29.
13. Jain, P. S., and Patel, A. J. Specificity assessment in UV analysis. International Journal of Analytical Chemistry. 2016; 3(2): 31-39.
14. Ghosh, R., and Pal, T. K. Analytical method validation: Regulatory perspectives. Indian Journal of Pharmaceutical Sciences. 2015; 77(5): 636-640.
15. Snyder, L. R., and Kirkland, J. J. Introduction to Modern Liquid Chromatography. 3rd ed. Wiley. 2010
16. Indian Pharmacopoeia Commission. Indian Pharmacopoeia 2018, Vol. II. Ghaziabad: Government of India Press. 2018
17. Patel S, Soni N, Patel P. Development and validation of UV spectrophotometric method for estimation of amlodipine besylate in bulk and tablet dosage form. Int J Pharm Sci Res. 2012; 3(7): 2381-6.
18. Shinde PP, Pawar PS, Kumbhar AS. Development and validation of a UV spectrophotometric method for the determination of amlodipine in tablet dosage form. J Pharm Biomed Anal. 2011; 54(5): 847-51.
19. Jain JB, Phadke SB, Rane PS. Spectrophotometric methods for the analysis of amlodipine besylate in bulk and dosage forms. Int J Drug Dev Res. 2014; 6(1): 1-6.
20. Reddy SVRR, Reddy SMSR, Reddy KRS. Development and validation of a UV-visible spectrophotometric method for estimation of amlodipine in tablets. Asian J Res Chem. 2009; 2(1): 118-20.
21. Sastry URS, Reddy SG. UV spectrophotometric methods for the estimation of amlodipine in pharmaceutical formulations. J Anal Bioanal Tech. 2015; 6(4):287-94.