Abstract
Background . Today, many studies reflect an increase in the antibacterial effect of drugs through the use of a colloidal solution of silver nanoparticles. Creation of the various forms of drugs for an external use with a slow-release active component and antibacterial activity is relevant and promising for use in the treatment of superficial wounds and injuries. Objective . Synthesis and stabilization of quasispherical silver nanoparticles for external applications. Design and methods . The citrate method was used for the synthesis of colloidal silver. Dosage forms of external use were prepared by several methods: reaction with albumin, liposomal form, thickening with Aerosil and incorporation into microspheres. Results . Several methods of possible preparation of finished dosage forms based on colloidal silver nanoparticles have been demonstrated: reaction with albumin, liposomal form, thickening with Aerosil and incorporation into microspheres. Conclusion . Further investigation of both antimicrobial activity and cytotoxicity will reveal dosage forms with optimal efficiency/safety ratio.
Highlights
many studies reflect an increase in the antibacterial effect of drugs
The citrate method was used for the synthesis of colloidal silver
Dosage forms of external use were prepared by several methods
Summary
Many studies reflect an increase in the antibacterial effect of drugs through the use of a colloidal solution of silver nanoparticles. Одним из направлений является использование препаратов серебра, прежде всего в форме коллоидного раствора наночастиц. В настоящее время препараты на основе AgNP (наночастиц серебра) переживают второе рождение. Исследование было проведено для изучения антибактериальных свойств наночастиц коллоидного серебра и эвгенола, отдельно и в комбинации, на Staphylococcus aureus и Salmonella Typhimurium и их взаимодействиях с пищевыми компонентами (жир, белок и углеводы) [1].
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