The Forced Degradation Study in Pharmaceutical Stability is a process where the chemical properties of the parent drug are investigated using ultra-filtration and solvent techniques. This process can be used to identify and profile all types of stability processes during the drug growth and development course. Various parameters such as equilibrium, conformability, density, and electronic charges are determined on both the parent drug and its derivatives during this process. This study is therefore significant for the pharmaceutical industry.
The Forced Degradation study in Pharmaceutical Stability is a non-inquisitional method. This means that no consideration is given to the equilibrium or the structure of the drug during this process. This process is used for the chemical identification of all types of single-site or at-site reactions that can take place between any two different medicines which have not been pretreated. For instance, the response of tetracycline with methionine, sulfate, glycine, or any other amino acid can be studied using this method.