Study of the stability of a pharmaceutical composition based on a liposomal system under various storage conditions

Abstract

The aim of the work is to investigate the stability of liposomal vitamin C in the form of solid capsules obtained using the developed technology, with an assessment of the main physicochemical indicators: appearance, active ingredient content, mass homogeneity and disintegration under different storage conditions. The study will determine the preservation of pharmacotechnological properties and assess the suitability of the drug for further use and industrial production.