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

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Summary

Introduction

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].

Results
Conclusion

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