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Development and characterization of niosomal gel of fusidic acid: in-vitro and ex-vivo approaches
Niosomes are multilamellar vesicles that efficiently deliver active substance into skin systemic circulation or skin layers. They are used in topical drug delivery system to enhance the skin permeation of active substance. So, the prime objective of this study was to develop a niosomal gel of fusidi...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Taylor & Francis
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9196814/ https://www.ncbi.nlm.nih.gov/pubmed/35711622 http://dx.doi.org/10.1080/15685551.2022.2086411 |
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author | Waqas, Muhammad Khurram Sadia, Haleema Khan, Muhammad Imran Omer, Muhammad Ovais Siddique, Muhammad Irfan Qamar, Shaista Zaman, Muhammad Butt, Muhammad Hammad Mustafa, Mian Waqar Rasool, Naeem |
author_facet | Waqas, Muhammad Khurram Sadia, Haleema Khan, Muhammad Imran Omer, Muhammad Ovais Siddique, Muhammad Irfan Qamar, Shaista Zaman, Muhammad Butt, Muhammad Hammad Mustafa, Mian Waqar Rasool, Naeem |
author_sort | Waqas, Muhammad Khurram |
collection | PubMed |
description | Niosomes are multilamellar vesicles that efficiently deliver active substance into skin systemic circulation or skin layers. They are used in topical drug delivery system to enhance the skin permeation of active substance. So, the prime objective of this study was to develop a niosomal gel of fusidic acid to increase its skin permeation. Different formulations of niosomes of fusidic acid were designed by varying the cholesterol to surfactant ratio. Formulations containing fusidic acid, cholesterol, dihexadecyl pyridinium chloride, Span 60, or Tween 60 were prepared by thin film hydration method in rotary evaporator. The thin film formed in rotary flask was hydrated by phosphate buffer saline of pH 7.2. The niosomes formed were characterized through entrapment efficiency, size, polydispersity index (PDI), and zeta potential. The S3 formulation containing span 60 showed the highest entrapment efficiency (EE) of niosomes, so it was incorporated into Carbopol gel. Determination of pH, spreadability, rheological, and ex vivo permeation studies was conducted of niosomal gel. The results of ex vivo permeation studies showed high permeation of fusidic acid when gel was applied to an albino rat skin. According to the results and previous studies of niosomes, it can be concluded that niosomes enhanced the permeation of fusidic acid through the skin. |
format | Online Article Text |
id | pubmed-9196814 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Taylor & Francis |
record_format | MEDLINE/PubMed |
spelling | pubmed-91968142022-06-15 Development and characterization of niosomal gel of fusidic acid: in-vitro and ex-vivo approaches Waqas, Muhammad Khurram Sadia, Haleema Khan, Muhammad Imran Omer, Muhammad Ovais Siddique, Muhammad Irfan Qamar, Shaista Zaman, Muhammad Butt, Muhammad Hammad Mustafa, Mian Waqar Rasool, Naeem Des Monomers Polym Full Length Article Niosomes are multilamellar vesicles that efficiently deliver active substance into skin systemic circulation or skin layers. They are used in topical drug delivery system to enhance the skin permeation of active substance. So, the prime objective of this study was to develop a niosomal gel of fusidic acid to increase its skin permeation. Different formulations of niosomes of fusidic acid were designed by varying the cholesterol to surfactant ratio. Formulations containing fusidic acid, cholesterol, dihexadecyl pyridinium chloride, Span 60, or Tween 60 were prepared by thin film hydration method in rotary evaporator. The thin film formed in rotary flask was hydrated by phosphate buffer saline of pH 7.2. The niosomes formed were characterized through entrapment efficiency, size, polydispersity index (PDI), and zeta potential. The S3 formulation containing span 60 showed the highest entrapment efficiency (EE) of niosomes, so it was incorporated into Carbopol gel. Determination of pH, spreadability, rheological, and ex vivo permeation studies was conducted of niosomal gel. The results of ex vivo permeation studies showed high permeation of fusidic acid when gel was applied to an albino rat skin. According to the results and previous studies of niosomes, it can be concluded that niosomes enhanced the permeation of fusidic acid through the skin. Taylor & Francis 2022-06-09 /pmc/articles/PMC9196814/ /pubmed/35711622 http://dx.doi.org/10.1080/15685551.2022.2086411 Text en © 2022 The Author(s). Published by Informa UK Limited, trading as Taylor & Francis Group. https://creativecommons.org/licenses/by/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) ), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Full Length Article Waqas, Muhammad Khurram Sadia, Haleema Khan, Muhammad Imran Omer, Muhammad Ovais Siddique, Muhammad Irfan Qamar, Shaista Zaman, Muhammad Butt, Muhammad Hammad Mustafa, Mian Waqar Rasool, Naeem Development and characterization of niosomal gel of fusidic acid: in-vitro and ex-vivo approaches |
title | Development and characterization of niosomal gel of fusidic acid: in-vitro and ex-vivo approaches |
title_full | Development and characterization of niosomal gel of fusidic acid: in-vitro and ex-vivo approaches |
title_fullStr | Development and characterization of niosomal gel of fusidic acid: in-vitro and ex-vivo approaches |
title_full_unstemmed | Development and characterization of niosomal gel of fusidic acid: in-vitro and ex-vivo approaches |
title_short | Development and characterization of niosomal gel of fusidic acid: in-vitro and ex-vivo approaches |
title_sort | development and characterization of niosomal gel of fusidic acid: in-vitro and ex-vivo approaches |
topic | Full Length Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9196814/ https://www.ncbi.nlm.nih.gov/pubmed/35711622 http://dx.doi.org/10.1080/15685551.2022.2086411 |
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