DEVELOPMENT AND IN VITRO EVALUATION OF MICONAZOLE ETHOSOMAL GEL

  • Unique Paper ID: 206466
  • Volume: 13
  • Issue: 2
  • PageNo: 1852-1860
  • Abstract:
  • The present study was focused on formulating and evaluating Miconazole containing ethosomal gel formulation for in vitro studies. Ethosomal formulations were prepared by using cold method and were evaluated for in vitro characteristics, stability studies. Ethosomal formulation displayed highest entrapment efficiency with desired particle size. SEM analyses showed that ethosomal formulation was spherical in shape. Ethosomes containing lipid higher percentage of drug release after 8 h as compared to other formulations. F-3 formulation was found to be stable at the end of the study on storage condition. The present study suggested that ethosomal gel formulations provide sustained and prolonged delivery of drug with enhance bioavailability.

Copyright & License

Copyright © 2026 Authors retain the copyright of this article. This article is an open access article distributed under the Creative Commons Attribution License which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

BibTeX

@article{206466,
        author = {PALLE MOULIKA},
        title = {DEVELOPMENT AND IN VITRO EVALUATION OF MICONAZOLE ETHOSOMAL GEL},
        journal = {International Journal of Innovative Research in Technology},
        year = {2026},
        volume = {13},
        number = {2},
        pages = {1852-1860},
        issn = {2349-6002},
        url = {https://ijirt.org/article?manuscript=206466},
        abstract = {The present study was focused on formulating and evaluating Miconazole containing ethosomal gel formulation for in vitro studies. Ethosomal formulations were prepared by using cold method and were evaluated for in vitro characteristics, stability studies.  Ethosomal formulation displayed highest entrapment efficiency with desired particle size. SEM analyses showed that ethosomal formulation was spherical in shape. Ethosomes containing lipid higher percentage of drug release after 8 h as compared to other formulations. F-3 formulation was found to be stable at the end of the study on storage condition. The present study suggested that ethosomal gel formulations provide sustained and prolonged delivery of drug with enhance bioavailability.},
        keywords = {Ethosomal gel, Miconazole, bioavailability, cold technique, in vitro drug release studies.},
        month = {July},
        }

Cite This Article

MOULIKA, P. (2026). DEVELOPMENT AND IN VITRO EVALUATION OF MICONAZOLE ETHOSOMAL GEL. International Journal of Innovative Research in Technology (IJIRT), 13(2), 1852–1860.

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