Published Paper Details:

Abstract: Analytical method development and validation plays an important role in the discovery, development and manufacture of pharmaceuticals. These methods used to ensure the identity, purity, potency and performance of drug products. In the present study, a successful attempt was made for the HPLC quantitative estimation of Diloxanide furoate in bulk formulation. The method was developed by experimentation based on thorough literature survey and ascertained by statistical parameters of sampling. The entire work was performed on waters HPLC with U.V. Vis detector. The result obtained shows the developed method to be precise, simple, rapid and accurate. Thus these can be used for routine analysis of Diloxanide furoate in bulk drug dosage form. It was thus, concluded that the proposed method is new, simple, accurate, safe, free form pollution, precise and can be successfully employed in the routine analysis. The simplicity, rapidity reproducibility and economy of the proposed methods completely fulfill the objective of this research work.