Validation of newly developed analytical method for standardization of cajanin using RP-HPLC method in prepared extract

Authors

  • Sereya Koneru Research Scholar, Krishna University, Krishna District, Andhra Pradesh, India
  • G. Devala Rao Department of Pharmaceutical Analysis, K.V.S.R Siddhartha College of Pharmaceutical Sciences, Vijayawada, Andhra Pradesh, India
  • Sujatha Palatheeya Department of Pharmacy, University College of Pharmaceutical Sciences, Palamuru University, Mahbubnagar, Telangana, India

Keywords:

Cajanin, Spectrophotometric method, Method development and validation, RP-HPLC method, ICH guidelines

Abstract

In this study, a simple, precise and accurate analytical method was developed and validated for identification of Cajanin using RP-HPLC method in prepared extract. Spectrophotometric determination was performed on a Perkin-Elmer UV-VIS Double Beam Spectrophotometer to know the maximum absorbance of the compounds. Chromatographic separation was performed using merck C18 analytical column (5 μm, 250 mm x 4.6 mm, i.d). Phosphate buffer at pH 3.5 and acetonitrile in the ratio of 30:70 v/v was considered to be suitable solvent system. The flow rate was maintained at 0.8ml/min. The effluents were detected by means of UV detector at 292nm. The calibration curves were linear at a range of 5 - 25µg/ml with significant correlation coefficient of 0.9966. The retention time was found to be at 4.14min. The method was validated according to ICH guidelines and was found to contain the %RSD values below 2% which shows that the method was precise, specific and accurate.

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Published

2020-12-22

How to Cite

Sereya Koneru, G. Devala Rao, & Sujatha Palatheeya. (2020). Validation of newly developed analytical method for standardization of cajanin using RP-HPLC method in prepared extract. World Journal of Pharmaceutical Sciences, 9(1), 67–71. Retrieved from https://wjpsonline.com/index.php/wjps/article/view/81

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Section

Research Article