DEVELOPMENT AND VALIDATION OF RP-HPLC METHOD FOR THE DETERMINATION OF LETROZOLE IN BULK AND DOSAGE FORM 

Journal Title: International Research Journal of Pharmacy (IRJP) - Year 2012, Vol 3, Issue 11

Abstract

A Reverse phase high performance liquid chromatographic method was developed for the determination of Letrozole in bulk and dosage form. The separation was effected on a kromasil ODS C18 column (250mmX4.6mm, 5μ) using a mobile phase mixture of buffer and methanol in a ratio of 85:15 v/v at a flow rate of 1.0ml/min. The detection was made at 230nm. The retention time of letrozole was found to be 3.443±0.08 min. Calibration curve was linear over the concentration range of 20-120μg/ml of Letrozole. The propose method was validated as per the ICH guidelines. The method was accurate, precise, specific and rapid found to be suitable for the quantitative analysis of the drug and dosage form.  

Authors and Affiliations

S Pallavi , PM Vasanth, T Ramesh , Ramesh Malothu

Keywords

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  • EP ID EP151093
  • DOI -
  • Views 114
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How To Cite

S Pallavi, PM Vasanth, T Ramesh, Ramesh Malothu (2012). DEVELOPMENT AND VALIDATION OF RP-HPLC METHOD FOR THE DETERMINATION OF LETROZOLE IN BULK AND DOSAGE FORM . International Research Journal of Pharmacy (IRJP), 3(11), 202-204. https://europub.co.uk/articles/-A-151093