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Enhanced skin permeation of glabridin using eutectic mixture-based nanoemulsion
Chen Liu1, Jin Hu1, Hong Sui2,3
1General Hospital of Ningxia Medical University, Yinchuan, Ningxia, 750004, China.
Drug Delivery and Translational Research
|February 12, 2017
Summary
A menthol-camphor eutectic mixture in nanoemulsions significantly enhances glabridin transdermal delivery. This formulation offers superior skin penetration compared to traditional methods, proving effective for water-insoluble drugs.
Area of Science:
- Pharmaceutical Sciences
- Materials Science
- Dermatology
Background:
- Glabridin, a water-insoluble compound, faces challenges in transdermal delivery.
- Nanoemulsions offer potential for improved drug solubilization and skin penetration.
- Eutectic mixtures can enhance the solubility and delivery of poorly soluble drugs.
Purpose of the Study:
- To evaluate a menthol-camphor eutectic mixture within a nanoemulsion for enhanced transdermal delivery of glabridin.
- To compare the performance of this nanoemulsion with conventional formulations.
- To optimize and characterize the nanoemulsion for stability and skin permeation.
Main Methods:
- Solubility of glabridin was determined using the shaking bottle method.
- Pseudoternary phase diagrams were constructed to identify nanoemulsion regions.
- Nanoemulsions were formulated, characterized for particle size, and tested for in vitro/in vivo skin permeation.
- Storage stability was assessed over three months.
Main Results:
- Optimized nanoemulsion contained 0.25% glabridin, 5% oil phase, 10% Tween 80, 5% glycerol, and 79.75% water.
- Nanoemulsions achieved a mean droplet size of approximately 100 nm.
- The eutectic mixture nanoemulsion showed significantly higher in vitro skin permeability (28.26 μg/cm²) compared to IPM (9.94 μg/cm²) and drug solution (3.82 μg/cm²).
- In vivo studies confirmed enhanced transdermal delivery.
Conclusions:
- The menthol-camphor eutectic mixture is an effective solubilizer for glabridin.
- Nanoemulsions utilizing this eutectic mixture serve as superior nanocarriers for glabridin transdermal delivery.
- This approach holds promise for improving the efficacy of poorly soluble drugs via the transdermal route.
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