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Potentiating antimicrobial efficacy of propolis through niosomal-based system for administration
BACKGROUND: Propolis is a multicomponent active, complex resinous substance collected by honeybees (Apis mellifera) from a variety of plant sources. This study was designed to improve the antimicrobial efficacy of propolis by engineering a niosomal-based system for topical application. METHODS: Prop...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5481798/ https://www.ncbi.nlm.nih.gov/pubmed/28664114 http://dx.doi.org/10.1016/j.imr.2014.10.004 |
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author | Patel, Jay Ketkar, Sameer Patil, Sharvil Fearnley, James Mahadik, Kakasaheb R. Paradkar, Anant R. |
author_facet | Patel, Jay Ketkar, Sameer Patil, Sharvil Fearnley, James Mahadik, Kakasaheb R. Paradkar, Anant R. |
author_sort | Patel, Jay |
collection | PubMed |
description | BACKGROUND: Propolis is a multicomponent active, complex resinous substance collected by honeybees (Apis mellifera) from a variety of plant sources. This study was designed to improve the antimicrobial efficacy of propolis by engineering a niosomal-based system for topical application. METHODS: Propolis was extracted in ethanol and screened for total polyphenol content. Propolis-loaded niosomes (PLNs) were prepared with varying concentrations of Span 60 and cholesterol. The PLNs were evaluated for physicochemical parameters, namely, vesicle size, entrapment efficiency, zeta potential, surface topography and shape, and stability, followed by screening for in vitro antimicrobial activity. The PLNs were formulated into propolis niosomal gel (PNG) using Carbopol P934 base and subjected to ex vivo skin deposition study. RESULTS: The ethanolic extract of propolis had high polyphenolic content (270 ± 9.2 mg GAE/g). The prepared PLNs showed vesicle size between 294 nm and 427 nm, and the percent entrapment in the range of 50.62–71.29% with a significant enhancement in antimicrobial activity against Staphylococcus aureus and Candida albicans. Enhanced antimicrobial activity of PLNs was attributed to the ability of niosomes to directly interact with the bacterial cell envelop thereby facilitating the diffusion of propolis constituents across the cell wall. The formulated PNG exhibited a twofold better skin deposition due to improved retention of niosomes in the skin. CONCLUSION: The findings indicate that the engineering of a niosomal-based system for propolis enhanced its antimicrobial potential through topical application. |
format | Online Article Text |
id | pubmed-5481798 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | Elsevier |
record_format | MEDLINE/PubMed |
spelling | pubmed-54817982017-06-29 Potentiating antimicrobial efficacy of propolis through niosomal-based system for administration Patel, Jay Ketkar, Sameer Patil, Sharvil Fearnley, James Mahadik, Kakasaheb R. Paradkar, Anant R. Integr Med Res Original Article BACKGROUND: Propolis is a multicomponent active, complex resinous substance collected by honeybees (Apis mellifera) from a variety of plant sources. This study was designed to improve the antimicrobial efficacy of propolis by engineering a niosomal-based system for topical application. METHODS: Propolis was extracted in ethanol and screened for total polyphenol content. Propolis-loaded niosomes (PLNs) were prepared with varying concentrations of Span 60 and cholesterol. The PLNs were evaluated for physicochemical parameters, namely, vesicle size, entrapment efficiency, zeta potential, surface topography and shape, and stability, followed by screening for in vitro antimicrobial activity. The PLNs were formulated into propolis niosomal gel (PNG) using Carbopol P934 base and subjected to ex vivo skin deposition study. RESULTS: The ethanolic extract of propolis had high polyphenolic content (270 ± 9.2 mg GAE/g). The prepared PLNs showed vesicle size between 294 nm and 427 nm, and the percent entrapment in the range of 50.62–71.29% with a significant enhancement in antimicrobial activity against Staphylococcus aureus and Candida albicans. Enhanced antimicrobial activity of PLNs was attributed to the ability of niosomes to directly interact with the bacterial cell envelop thereby facilitating the diffusion of propolis constituents across the cell wall. The formulated PNG exhibited a twofold better skin deposition due to improved retention of niosomes in the skin. CONCLUSION: The findings indicate that the engineering of a niosomal-based system for propolis enhanced its antimicrobial potential through topical application. Elsevier 2015-06 2014-10-30 /pmc/articles/PMC5481798/ /pubmed/28664114 http://dx.doi.org/10.1016/j.imr.2014.10.004 Text en © 2015 Korea Institute of Oriental Medicine. Published by Elsevier. http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/). |
spellingShingle | Original Article Patel, Jay Ketkar, Sameer Patil, Sharvil Fearnley, James Mahadik, Kakasaheb R. Paradkar, Anant R. Potentiating antimicrobial efficacy of propolis through niosomal-based system for administration |
title | Potentiating antimicrobial efficacy of propolis through niosomal-based system for administration |
title_full | Potentiating antimicrobial efficacy of propolis through niosomal-based system for administration |
title_fullStr | Potentiating antimicrobial efficacy of propolis through niosomal-based system for administration |
title_full_unstemmed | Potentiating antimicrobial efficacy of propolis through niosomal-based system for administration |
title_short | Potentiating antimicrobial efficacy of propolis through niosomal-based system for administration |
title_sort | potentiating antimicrobial efficacy of propolis through niosomal-based system for administration |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5481798/ https://www.ncbi.nlm.nih.gov/pubmed/28664114 http://dx.doi.org/10.1016/j.imr.2014.10.004 |
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