Topical Nanoemulgel for the Treatment of Skin Cancer: Proof-of-Technology
Sreeharsha Nagaraja1,2, Girish Meravanige Basavarajappa3, Mahesh Attimarad1
1Department of Pharmaceutical Sciences, College of Clinical Pharmacy, King Faisal University, Al-Hofuf, Al-Ahsa 31982, Saudi Arabia.
Abstract:
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.
Insights
This study developed a novel chrysin nanoemulgel for effective topical treatment of melanoma. The advanced delivery system enhances skin permeation and therapeutic efficacy while reducing dosage.
Area of Science:
- Pharmaceutics
- Dermatology
- Nanotechnology
Background:
- Current skin cancer treatments suffer from systemic side effects and poor skin penetration.
- Novel nanocarrier development is crucial for overcoming these limitations.
Purpose of the Study:
- To validate a novel proof-of-technology for topical chrysin nanoemulgel delivery.
- To develop an efficient treatment for melanoma-affected skin with enhanced localized delivery.
Main Methods:
- Formulation of a chrysin-loaded nanocomplex in a Pluronic F-127 gel base.
- Optimization using pseudo-ternary phase diagrams with specific surfactants and co-solvents.
- Characterization of physicochemical properties, including droplet size, polydispersity, and viscosity.
Main Results:
- The nanoemulgel exhibited a stable, self-emulsifying system with a mean droplet size of 156.9 nm.
- Significant improvements in ex vivo skin permeation and drug deposition were observed.
- In vitro studies demonstrated enhanced cytotoxicity against melanoma cell lines (A375, SK-MEL-2) and confirmed biocompatibility.
Conclusions:
- Aqueous, gel-based, topical nanoemulsified chrysin offers a promising approach for localized skin cancer treatment.
- This technology can reduce treatment frequency and dosage, improving the therapeutic index.
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