Development of an UV spectroscopic method for Capsaicin quantification in dosage form and in a bulk formulation

Pharmaceutical Science-Pharmaceutical Analysis

Authors

  • Atul Baravkar Agricultural Development Trust’s Shardabai Pawar Institute of Pharmaceutical Sciences & Research, Baramati, India. 413115 https://orcid.org/0000-0002-0469-9838
  • Vitthal Chopade PES Modern college of Pharmacy, Nigdi, Pune, India. 411044
  • Sneha Dhonde PES Modern college of Pharmacy, Nigdi, Pune, India. 411044
  • Trushali Mandhare Career Point University, Kota, Rajasthan, India. 324005
  • Pooja Kashid Career Point University, Kota, Rajasthan, India. 324005
  • Ganesh Phadtare Career Point University, Kota, Rajasthan, India. 324005
  • Jyoti Jawale Institute of Pharmaceutical Sciences and Research for Girls, Bhigwan, Pune, India. 413130
  • Alfa Jain Institute of Pharmaceutical Sciences and Research for Girls, Bhigwan, Pune, India. 413130
  • Deepali Kadam K. K. Wagh College of Pharmacy, Nashik, India. 422006
  • Aditi Zagade SVPM’s College of Pharmacy, Baramati, India. 413115

DOI:

https://doi.org/10.22376/ijlpr.2023.13.3.P62-P69

Keywords:

Capsaicin, UV method, Validation, Spectrophotometry, Stress degradation, Calibration curve.

Abstract

A proper procedure must be created to make sure that capsaicin, whether in dosage form or in bulk, can be identified. The method development makes sure that the amount of a capsaicin can be simply determined. To determine validation parameters like accuracy, precision, LOD, LOQ, recovery study and range for capsaicin. In the present study a proper UV Spectroscopic method was developed and validated for determination of capsaicin. UV Spectrophotometric method was done at 280nm and samples were prepared with Methanol. The linearity demonstrated a correlation coefficient of 0.9922 various validation parameters like accuracy, precision, LOD, LOQ, recovery study and range were found to be within the specified range. The proposed method was simple, rapid, precise, accurate and sensitive and can be used for routine analysis of capsaicin. 

References

Victor F, Mirian SN, Ana CR, Felope AP, Waldiceu AV, Duan JA.- Capsaicin: current understanding of its mechanisms and therapy of pain and other pre-clinical and clinical uses. Chemical Analysis of the Herbal Medicine Salviae miltiorrhizae Radix et Rhizoma (Danshen). Molecules. 2016 Jan 5;21(1):513:1-2. doi: 10.3390/molecules21010051, PMID 26742026.

David GW. Pharmaceutical analysis. 5th ed. Elsevier/Churchill Livingstone & Livingstone; 2012. p. 1-20.

Beckett AH, Stenlake JB. Practice pharmaceutical chemistry. 3rd ed. New Delhi: CBS Publisher; 1997. p. 2858.

Shoaeb S, Mubashir M. Validation of UV spectrophotometric method for determination of atenolol. Int J Pharmacol Res. 2014 Feb:61:25-7.

Jadhav AS, Tarkase KN, Deshpande AP. Quantitative determination of metoprolol succinate in bulk and tablet dosage form through comparative study of UV and derivative spectroscopy. Der Pharm Let. 2012 Sep:43:763-7.

Moreshwar NK, Rajeshwar VK, Dinesh MS. Development and validation of spectrophotometric method for determination of metoprolol succinate. Int J ChemTech Res. 2009 Aug:14:1273-7.

ICH. Q2 (R1) validation of analytical procedure: text and methodology, international Conference on Harmonization, Geneva, Switzerland. 2005.

Mitesh DP, Purnima DH. A validated and simplified RPHPLC of metoprolol succinate from bulk drugs. Asian JRes Chem. 2009 Jan:22:119-22.

Rahman N, Rahman H, Aami SN. Validated kinetic spectrophotometric method for the determination of metoprolol tartarate in pharmaceutical formulations. Chem Pharm Bull. 2005 Mar:538:942-8.

Sandberg A, Ragnarsson G, Jonsson UE, Sjögren J. Design of a new multiple unit controlled release formulation of metoprolol CR. Eur J Clin Pharmacol. 1988 Feb;33;Suppl:S3-7. doi: 10.1007/BF00578405, PMID 3371391.

Vora BN, Parmar RR, Nayak PP, Shah DA. Development and validation of the simultaneous UV spectrophotometric method for estimation of metoprolol succinate and olmesartan medoxomil in the tablet dosage form. Pharm Methods. 2012 Aug;3(1):44-7. doi: 10.4103/2229-4708.97724, PMID 23781477.

ICH. Q1A. 1996;R2 stability testing of new drug substances and products, International conference on harmonization; Nov.

Published

2023-05-01

How to Cite

Baravkar, A. ., Chopade, V. ., Dhonde, S. ., Mandhare, T. ., Kashid, P. ., Phadtare, G. ., Jawale, J. ., Jain, A. ., Kadam, D. ., & Zagade, A. . (2023). Development of an UV spectroscopic method for Capsaicin quantification in dosage form and in a bulk formulation: Pharmaceutical Science-Pharmaceutical Analysis. International Journal of Life Science and Pharma Research, 13(3), P62-P69. https://doi.org/10.22376/ijlpr.2023.13.3.P62-P69

Issue

Section

Research Articles