Development and validation of the UV spectroscopic method for varenicline determination in pharmaceutical preparation

https://doi.org/10.53730/ijhs.v6nS8.14227

Authors

  • Prakruti Mukund Amin GTU Research Scholar, Gujarat Technological University, Ahmedabad, Gujarat, India | K.B. Institute of Pharmaceutical Education and Research, Gandhinagar, Gujarat, India
  • Manish Patel Department of Pharmaceutics, L. M. College of Pharmacy, Gujarat Technological University, Ahmedabad, Gujarat, India

Keywords:

UV visible spectroscopic method, varenicline, smocking

Abstract

A simple and accurate UV visible spectroscopic method has been developed and validated for quantification of varenicline in bulk drug and pharmaceutical dosage forms.  A shimadzu UV spectrophotometer was used considering availability and cost effectiveness of the proposed method. λmax  of 236nm  and   319nm  were    observed  from    the   spectroscopic  method.  The calibration curve was linear (r = 0.99) in the studied range of concentration (5- 40 µg /ml) in both the absorption maxima. The selectivity and sensitivity of the elaborated method were satisfactory, and the limits of detection and quantification were   less than 20% of the specification level.   Moreover, the inter-  and  intra-day precisions was  found  to be  less  than  3%  (RSD),  while  the recovery values  expressing inter-  and intra-day accuracy was varied  from 99.73  to 101.23. The varenicline solution was stable over a period of 3 days on storage under refrigeration. The utility of the developed method was examined by analyzing the tablets containing VAR.  As a result, the method was found to be selective, sensitive, precise and accurate.

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Published

25-06-2022

How to Cite

Amin, P. M., & Patel, M. (2022). Development and validation of the UV spectroscopic method for varenicline determination in pharmaceutical preparation. International Journal of Health Sciences, 6(S8), 7049–7057. https://doi.org/10.53730/ijhs.v6nS8.14227

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Section

Peer Review Articles