Abstract

Stability Indicating Analytic Method Devlompent & Validation of Hplc

Author: Dhara P. Patel

Doi: 10.62655/s-epub.2021.v13.i02.pp1-7

Abstract:

When it comes to analysing the stability of a pharmacological product or doing quantitative and qualitative analyses of it, high-performance liquid chromatography is among the most reliable procedures. The purpose of these is to isolate and remove any traces of drug-related contaminants that may have been introduced during the production process. Strategies and difficulties related to the development of stability-indicating HPLC systems for pharmacological substances are discussed in this article. Forced degradation investigations of novel chemical entities and pharmaceutical items are necessary for the development and specificity of such a stability indicating approach.