Abstract

This study describes a systemic approach for the formulation and evaluation of Efavirenz tablets and has been done in this work using Moringa Oleifera as a natural polymer at different concentrations. In order to identify the medication, melting point, solubility, and FTIR analysis were used. DSC was used for investigating the drug polymer interactions. Consequently, no interaction between the medicine and polymer used in the formulation was detected. The formulations were created by blending medication and excipients, then analysing them for Angle of repose, Bulk density, Tapered bulk density, Hausner's ratio, and Carr's compressibility index. The powder blends passed all of these tests with flying colours. Direct compression was used to make the seven batches of Efavirenz pills. Thickness, hardness, friability, weight variation, and drug content were all measured on the manufactured tablets. All of the values were found to be within the parameters. All seven batches were subjected to in-vitro dissolving tests. Because Formulation F7 has the largest percentage of medication release, it has been chosen as the best formulation. Stability tests were performed on the optimised formulation F7, and the findings showed no significant changes throughout the course of the three-month investigation. KEYWORDS: Efavirenz, Moringa oleifera, Formulation, Evaluation studies

Full Text
Paper version not known

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call

Disclaimer: All third-party content on this website/platform is and will remain the property of their respective owners and is provided on "as is" basis without any warranties, express or implied. Use of third-party content does not indicate any affiliation, sponsorship with or endorsement by them. Any references to third-party content is to identify the corresponding services and shall be considered fair use under The CopyrightLaw.