Abstract

Objective: This study aims to formulate and characterize a transfersome apple peel extract, formulate it into a gel, and compare it with a control gelmade without transfersome.Methods: Both gels were evaluated, stability tested, and penetration tested using Franz diffusion cells on the skin of female Sprague-Dawley rats. Thetransfersome preparations were formulated with different concentrations of the active substance, quercetin: 0.5% (F1); 0.7% (F2), and 1.0% (F3).Results: Based on the characterization results, F1 was selected as the optimum gel formulation because it had spherical morphology, a Dmean volume of106.44±2.70 nm, a polydispersity index of 0.078±0.01, a zeta potential of −49.96±2.05 mV, and a drug efficiency entrapment percentage of 78.78±0.46%.The cumulative amount of quercetin that was penetrated with the transfersome gel was 1514.41±26.31 μg/cm2, whereas the penetration with thecontrol gel extract was 1133.62±18.96 μg/cm2. The cumulative percentages of the penetrated gel transfersome and gel extract were 78.40±1.89%and 49.89±0.88%, respectively. The fluxes of transfersome gel and control gel extract were 52.33±0.11 μg/cm²/hrs and 40.89±0.68 μg/cm²/hrs,respectively.Conclusions: Based on these results, it can be concluded that the gel with transfersome exhibited better penetration than the gel extract alone.

Highlights

  • A number of health problems, including premature aging of the skin, are related to the formation of free radicals that bind to cells [1]

  • Two factors - internal factors and external factors [2] - are correlated with the process of the formation-free radicals in the body

  • Reactive oxygen species (ROS) are able to bind with cell/tissue components, causing damage that results in various degenerative diseases such as respiratory obstruction, arthritis, heart disease, stroke, diabetes, and cancer, as well as premature aging of the skin

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Summary

Methods

Stability tested, and penetration tested using Franz diffusion cells on the skin of female Sprague-Dawley rats. The transfersome preparations were formulated with different concentrations of the active substance, quercetin: 0.5% (F1); 0.7% (F2), and 1.0% (F3)

Results
INTRODUCTION
RESULTS AND DISCUSSION
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