Analytical Method Development and Validation of Exemestane Tablet by UV Spectrophotometry

The present research work discusses the development and validation of a UV spectrophotometric method for Exemestane. Simple, accurate and cost efficient spectrophotometric method has been developed for the estimation of Exemestane in Tablet dosage form. The optimum conditions for the analysis of the...

Full description

Saved in:
Bibliographic Details
Main Authors: S. Angalaparameswari, V. S. Thiruvengadarajan, N. Amruth Kumar, M. Kutumbarao, S. Ramkanth, C. Madhusudhanachetty
Format: Article
Language:English
Published: Wiley 2012-01-01
Series:E-Journal of Chemistry
Online Access:http://dx.doi.org/10.1155/2012/782738
Tags: Add Tag
No Tags, Be the first to tag this record!
_version_ 1832554425608044544
author S. Angalaparameswari
V. S. Thiruvengadarajan
N. Amruth Kumar
M. Kutumbarao
S. Ramkanth
C. Madhusudhanachetty
author_facet S. Angalaparameswari
V. S. Thiruvengadarajan
N. Amruth Kumar
M. Kutumbarao
S. Ramkanth
C. Madhusudhanachetty
author_sort S. Angalaparameswari
collection DOAJ
description The present research work discusses the development and validation of a UV spectrophotometric method for Exemestane. Simple, accurate and cost efficient spectrophotometric method has been developed for the estimation of Exemestane in Tablet dosage form. The optimum conditions for the analysis of the drug were established. The maximum wavelength (λ max) was found to be 246 nm. The percentage recovery of Exemestane was in the 98.7±0.4. Beers law was obeyed in the concentration range of 2-14 µg/mL. Calibration curves shows a linear relationship between the absorbance and concentration. The line equation y=0.05954x+0.0000 with r2 of 0.9938 was obtained. Validation was performed according to ICH guidelines for Linearity, accuracy, precision, LOD and LOQ. The sample solution was stable up to 36 hours. The proposed method may be suitable for the analysis of Exemestane in tablet formulation for quality control purposes.
format Article
id doaj-art-74cb4ffc1a1b4511b7f08b0f66a9e47c
institution Kabale University
issn 0973-4945
2090-9810
language English
publishDate 2012-01-01
publisher Wiley
record_format Article
series E-Journal of Chemistry
spelling doaj-art-74cb4ffc1a1b4511b7f08b0f66a9e47c2025-02-03T05:51:28ZengWileyE-Journal of Chemistry0973-49452090-98102012-01-01942068207310.1155/2012/782738Analytical Method Development and Validation of Exemestane Tablet by UV SpectrophotometryS. Angalaparameswari0V. S. Thiruvengadarajan1N. Amruth Kumar2M. Kutumbarao3S. Ramkanth4C. Madhusudhanachetty5Department of Pharmaceutical Analysis, Annamacharya College of Pharmacy Rajampet—516 126, Kadapa district, Andhra Pradesh, IndiaDepartment of Pharmaceutical Analysis, Annamacharya College of Pharmacy Rajampet—516 126, Kadapa district, Andhra Pradesh, IndiaDepartment of Pharmaceutical Analysis, Annamacharya College of Pharmacy Rajampet—516 126, Kadapa district, Andhra Pradesh, IndiaDepartment of Pharmaceutical Analysis, Annamacharya College of Pharmacy Rajampet—516 126, Kadapa district, Andhra Pradesh, IndiaDepartment of Pharmaceutical Analysis, Annamacharya College of Pharmacy Rajampet—516 126, Kadapa district, Andhra Pradesh, IndiaDepartment of Pharmaceutical Analysis, Annamacharya College of Pharmacy Rajampet—516 126, Kadapa district, Andhra Pradesh, IndiaThe present research work discusses the development and validation of a UV spectrophotometric method for Exemestane. Simple, accurate and cost efficient spectrophotometric method has been developed for the estimation of Exemestane in Tablet dosage form. The optimum conditions for the analysis of the drug were established. The maximum wavelength (λ max) was found to be 246 nm. The percentage recovery of Exemestane was in the 98.7±0.4. Beers law was obeyed in the concentration range of 2-14 µg/mL. Calibration curves shows a linear relationship between the absorbance and concentration. The line equation y=0.05954x+0.0000 with r2 of 0.9938 was obtained. Validation was performed according to ICH guidelines for Linearity, accuracy, precision, LOD and LOQ. The sample solution was stable up to 36 hours. The proposed method may be suitable for the analysis of Exemestane in tablet formulation for quality control purposes.http://dx.doi.org/10.1155/2012/782738
spellingShingle S. Angalaparameswari
V. S. Thiruvengadarajan
N. Amruth Kumar
M. Kutumbarao
S. Ramkanth
C. Madhusudhanachetty
Analytical Method Development and Validation of Exemestane Tablet by UV Spectrophotometry
E-Journal of Chemistry
title Analytical Method Development and Validation of Exemestane Tablet by UV Spectrophotometry
title_full Analytical Method Development and Validation of Exemestane Tablet by UV Spectrophotometry
title_fullStr Analytical Method Development and Validation of Exemestane Tablet by UV Spectrophotometry
title_full_unstemmed Analytical Method Development and Validation of Exemestane Tablet by UV Spectrophotometry
title_short Analytical Method Development and Validation of Exemestane Tablet by UV Spectrophotometry
title_sort analytical method development and validation of exemestane tablet by uv spectrophotometry
url http://dx.doi.org/10.1155/2012/782738
work_keys_str_mv AT sangalaparameswari analyticalmethoddevelopmentandvalidationofexemestanetabletbyuvspectrophotometry
AT vsthiruvengadarajan analyticalmethoddevelopmentandvalidationofexemestanetabletbyuvspectrophotometry
AT namruthkumar analyticalmethoddevelopmentandvalidationofexemestanetabletbyuvspectrophotometry
AT mkutumbarao analyticalmethoddevelopmentandvalidationofexemestanetabletbyuvspectrophotometry
AT sramkanth analyticalmethoddevelopmentandvalidationofexemestanetabletbyuvspectrophotometry
AT cmadhusudhanachetty analyticalmethoddevelopmentandvalidationofexemestanetabletbyuvspectrophotometry