Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
1222638 | Journal of Pharmaceutical and Biomedical Analysis | 2009 | 7 Pages |
Abstract
A selective stability indicating HPLC method was developed and validated for quantification of impurities (process related and degradants) and assay determination of Exemestane. Stability indicating power of the method was established by forced degradation experiments and mass balance study. The chromatographic separation was achieved with Hypersil BDS-C-18 using gradient elution. The developed method is validated for parameters like accuracy, linearity, LOD, LOQ, ruggedness. Box–Behnken experimental design was applied to check the robustness of the method.
Related Topics
Physical Sciences and Engineering
Chemistry
Analytical Chemistry
Authors
R. Suresh Kumar, M. Narasimha Naidu, Kasa Srinivasulu, K. Raja Sekhar, M. Veerender, M.K. Srinivasu,