High-performance liquid chromatography (HPLC) is an essential analytical tool for evaluating drug stability. HPLC methods must be able to isolate, detect, and quantify drug-related degradation products that may form during storage or production, and identify drug-related impurities that may form during synthesis. .. This article describes strategies and challenges for designing HPLC methods to demonstrate drug stability. It will deepen our understanding of drugs and medicinal chemistry and demonstrate advances in stability that reflect an analytical approach. Several important chromatographic parameters were investigated to improve the detection of potentially related degradants. It is necessary to find suitable solvent and mobile phase samples that provide sufficient stability and compatibility with each component and potential impurities and degradants. This method should be carefully considered as it has the ability to distinguish between primary and secondary decomposers. The study of forced destruction of chemicals and new drugs is essential for the development and characterization of these immobilization methods. Practical guidance is provided at each stage of drug development to develop a forced-disposal protocol and avoid common issues that might impede data interpretation.
HPLC, Forced degradation, Stability indicating method
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