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Topical Nanoemulgel for the Treatment of Skin Cancer: Proof-of-Technology
The present study is a mechanistic validation of ‘proof-of-technology’ for the effective topical delivery of chrysin nanoemulgel for localized, efficient treatment of melanoma-affected skin. Background: Currently available treatments for skin cancer are inefficient due to systemic side effects and p...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8234434/ https://www.ncbi.nlm.nih.gov/pubmed/34207014 http://dx.doi.org/10.3390/pharmaceutics13060902 |
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author | Nagaraja, Sreeharsha Basavarajappa, Girish Meravanige Attimarad, Mahesh Pund, Swati |
author_facet | Nagaraja, Sreeharsha Basavarajappa, Girish Meravanige Attimarad, Mahesh Pund, Swati |
author_sort | Nagaraja, Sreeharsha |
collection | PubMed |
description | The present study is a mechanistic validation of ‘proof-of-technology’ for the effective topical delivery of chrysin nanoemulgel for localized, efficient treatment of melanoma-affected skin. Background: Currently available treatments for skin cancer are inefficient due to systemic side effects and poor transcutaneous permeation, thereby presenting a formidable challenge for the development of novel nanocarriers. Methods: We opted for a novel approach and formulated a nanocomplex system composed of hydrophobic chrysin dissolved in a lipid mix, which was further nanoemulsified in Pluronic(®) F-127 gel to enhance physicochemical and biopharmaceutic characteristics. Chrysin, a flavone extracted from passion flowers, exhibits potential anti-cancer activities; however, it has limited applicability due to its poor solubility. Pseudo-ternary phase diagrams were constructed to identify the best self-nanoemulsifying region by varying the compositions of oil, Caproyl(®) 90 surfactant, Tween(®) 80, and co-solvent Transcutol(®) HP. Chrysin-loaded nanoemulsifying compositions were characterized for various physicochemical properties. Results: This thermodynamically stable, self-emulsifying drug delivery system showed a mean droplet size of 156.9 nm, polydispersity index of 0.26, and viscosity of 9100 cps after dispersion in gel. Mechanical characterization using Texture Analyzer exhibited that the gel had a hardness of 487 g and adhesiveness of 500 g. Ex vivo permeation through rat abdominal skin revealed significant improvement in percutaneous absorption measured as flux, the apparent permeability coefficient, the steady-state diffusion coefficient, and drug deposition. In vitro cytotoxicity on A375 and SK-MEL-2 cell lines showed a significantly improved therapeutic effect, thus ensuring reduction in dose. The safety of the product was established through biocompatibility testing on the L929 cell line. Conclusion: Aqueous, gel-based, topical, nanoemulsified chrysin is a promising technology approach for effective localized transcutaneous delivery that will help reduce the frequency and overall dose usage and ultimately improve the therapeutic index. |
format | Online Article Text |
id | pubmed-8234434 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-82344342021-06-27 Topical Nanoemulgel for the Treatment of Skin Cancer: Proof-of-Technology Nagaraja, Sreeharsha Basavarajappa, Girish Meravanige Attimarad, Mahesh Pund, Swati Pharmaceutics Article The present study is a mechanistic validation of ‘proof-of-technology’ for the effective topical delivery of chrysin nanoemulgel for localized, efficient treatment of melanoma-affected skin. Background: Currently available treatments for skin cancer are inefficient due to systemic side effects and poor transcutaneous permeation, thereby presenting a formidable challenge for the development of novel nanocarriers. Methods: We opted for a novel approach and formulated a nanocomplex system composed of hydrophobic chrysin dissolved in a lipid mix, which was further nanoemulsified in Pluronic(®) F-127 gel to enhance physicochemical and biopharmaceutic characteristics. Chrysin, a flavone extracted from passion flowers, exhibits potential anti-cancer activities; however, it has limited applicability due to its poor solubility. Pseudo-ternary phase diagrams were constructed to identify the best self-nanoemulsifying region by varying the compositions of oil, Caproyl(®) 90 surfactant, Tween(®) 80, and co-solvent Transcutol(®) HP. Chrysin-loaded nanoemulsifying compositions were characterized for various physicochemical properties. Results: This thermodynamically stable, self-emulsifying drug delivery system showed a mean droplet size of 156.9 nm, polydispersity index of 0.26, and viscosity of 9100 cps after dispersion in gel. Mechanical characterization using Texture Analyzer exhibited that the gel had a hardness of 487 g and adhesiveness of 500 g. Ex vivo permeation through rat abdominal skin revealed significant improvement in percutaneous absorption measured as flux, the apparent permeability coefficient, the steady-state diffusion coefficient, and drug deposition. In vitro cytotoxicity on A375 and SK-MEL-2 cell lines showed a significantly improved therapeutic effect, thus ensuring reduction in dose. The safety of the product was established through biocompatibility testing on the L929 cell line. Conclusion: Aqueous, gel-based, topical, nanoemulsified chrysin is a promising technology approach for effective localized transcutaneous delivery that will help reduce the frequency and overall dose usage and ultimately improve the therapeutic index. MDPI 2021-06-18 /pmc/articles/PMC8234434/ /pubmed/34207014 http://dx.doi.org/10.3390/pharmaceutics13060902 Text en © 2021 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Nagaraja, Sreeharsha Basavarajappa, Girish Meravanige Attimarad, Mahesh Pund, Swati Topical Nanoemulgel for the Treatment of Skin Cancer: Proof-of-Technology |
title | Topical Nanoemulgel for the Treatment of Skin Cancer: Proof-of-Technology |
title_full | Topical Nanoemulgel for the Treatment of Skin Cancer: Proof-of-Technology |
title_fullStr | Topical Nanoemulgel for the Treatment of Skin Cancer: Proof-of-Technology |
title_full_unstemmed | Topical Nanoemulgel for the Treatment of Skin Cancer: Proof-of-Technology |
title_short | Topical Nanoemulgel for the Treatment of Skin Cancer: Proof-of-Technology |
title_sort | topical nanoemulgel for the treatment of skin cancer: proof-of-technology |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8234434/ https://www.ncbi.nlm.nih.gov/pubmed/34207014 http://dx.doi.org/10.3390/pharmaceutics13060902 |
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