Control de los parámetros físico químicos y biofarmacéuticos de comprimidos de enalapril 20 mg.

Abstract

Introduction: This research study outlines the quality control of Enalapril tablets which must comply with all the quality parameters since it is a drug to treat a risk disease. Information was compiled from the United States Pharmacopoeia (USP), and information from other trials of common drugs, to support the results obtained in the different trials.

Objective: The quality of different Enalapril 20 mg tablets was evaluated through different assays to detect possible problems related to the tablets.

Materials and methods: A methodology based on a descriptive bibliographic analysis was applied. An exhaustive search, compilation, and selection of current information available in several open-access scientific databases was conducted to compare laboratory results and better understand them.

Results: The results of the analyzed articles could show several aspects that complied with the pharmacopeia; however, physical factors could alter some results.

Conclusion: It could be concluded that the different commercial companies do comply with the requirements established by the USP for tablets; however, environmental factors that may alter the results should not be discarded