Cargando…

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...

Descripción completa

Detalles Bibliográficos
Autores principales: Nagaraja, Sreeharsha, Basavarajappa, Girish Meravanige, Attimarad, Mahesh, Pund, Swati
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2021
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
_version_ 1783714083326918656
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
work_keys_str_mv AT nagarajasreeharsha topicalnanoemulgelforthetreatmentofskincancerproofoftechnology
AT basavarajappagirishmeravanige topicalnanoemulgelforthetreatmentofskincancerproofoftechnology
AT attimaradmahesh topicalnanoemulgelforthetreatmentofskincancerproofoftechnology
AT pundswati topicalnanoemulgelforthetreatmentofskincancerproofoftechnology