Asian Journal of Research in Pharmaceutical Sciences
  • Year: 2024
  • Volume: 14
  • Issue: 1

Strategic approach for HPLC Method Development and Validation: Review

  • Author:
  • Amitkumar J. Vyas1, Dhruvi U. Parmar1,*, Ashok B. Patel2, Ajay I. Patel1, Ashvin V. Dudhrejiya1, Sunny R. Shah1
  • Total Page Count: 6
  • Published Online: May 13, 2024
  • Page Number: 71 to 76

1B. K. Mody Government Pharmacy College, Polytechnic Campus, Near Aji Dam, Rajkot, Gujarat, India

2Government Pharmacy College, Gandhinagar, Gujarat, India

*Corresponding Author E-mail: parmardhruvi24@gmail.com

Online Published on 13 May, 2024.

Abstract

High performance liquid chromatography (HPLC) is an analytical technique which is adept to separate, detect and quantify numerous pharmaceuticals and their related degradants. It is also used to identify and measure synthetic drugs, to minimise other impurities at the time of separation, and to separate manufactured medicines from drug-related contaminants. To improve the procedure, a number of chromatographic parameters were assessed. It is necessary to identify the best mobile phase, column, detector, buffer, wavelength, and gradient for the drug’s compatibility and stability with degradants and contaminants. This study discusses the significance of RP-HPLC in the development of analytical methods, their techniques, and a brief overview of the key chromatographic parameters that must be tuned for effective method development.

Keywords

High performance liquid chromatography (HPLC), Chromatographic parameters, Validation