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Intracellular uptake of EGCG-loaded deformable controlled release liposomes for skin cancer
M Marwah1, Y Perrie2, R K S Badhan3
1School of Life and Health Sciences, Aston University, Birmingham, UK.
Abstract:
Caucasian population groups have a higher propensity to develop skin cancer, and associated clinical interventions often present substantial financial burden on healthcare services. Conventional treatments are often not suitable for all patient groups as a result of poor efficacy and toxicity profiles. The primary objective of this study was to develop a deformable liposomal formulation, the properties of which being dictated by the surfactant Tween 20, for the dermal cellular delivery of epigallocatechin gallatein (EGCG), a compound possessing antineoplastic properties. The results demonstrated a significant (p ≤ 0.05) decrease in liposome deformability index (74 ± 8 to 37 ± 7) as Tween 20 loading increased from 0 to 10% w/w, indicating an increase in elasticity. EGCG release over 24-h demonstrated Tween 20 incorporation directly increased release from 13.7% ± 1.1% to 94.4% ± 4.9% (for 0 and 10% w/w Tween 20 respectively). Finally, we demonstrated DilC-loaded deformable liposomes were localized intracellularly within human dermal fibroblast and keratinocyte cells within 2 h. Thus, it was evident that deformable liposomes may aid drug penetration into dermal cells and would be useful in developing a controlled-release formulation.
Insights
This study developed deformable liposomes using Tween 20 for enhanced skin cancer treatment delivery. These liposomes improved drug release and cellular penetration, offering a promising new approach for dermal drug delivery.
Area of Science:
- Pharmaceutical Sciences
- Dermatology
- Nanotechnology
Background:
- Caucasian populations have a higher risk of skin cancer.
- Current treatments for skin cancer have limitations in efficacy and toxicity.
- There is a need for improved drug delivery systems for dermal applications.
Purpose of the Study:
- To develop a deformable liposomal formulation for dermal delivery of epigallocatechin gallate (EGCG).
- To investigate the effect of Tween 20 on liposome properties and EGCG release.
- To assess the intracellular localization of deformable liposomes in dermal cells.
Main Methods:
- Formulation of deformable liposomes with varying concentrations of Tween 20.
- Characterization of liposome deformability and elasticity.
- In vitro release studies of EGCG from liposomes over 24 hours.
- Confocal microscopy to visualize intracellular delivery of DilC-loaded liposomes in human dermal fibroblasts and keratinocytes.
Main Results:
- Increased Tween 20 concentration significantly decreased liposome deformability index, enhancing elasticity.
- Tween 20 incorporation markedly increased EGCG release over 24 hours.
- Deformable liposomes were successfully localized intracellularly within dermal cells within 2 hours.
Conclusions:
- Deformable liposomes formulated with Tween 20 demonstrate enhanced drug release and improved dermal cellular penetration.
- This formulation holds potential for developing effective controlled-release topical treatments for skin conditions.
- The findings suggest a promising strategy for overcoming limitations of conventional dermal drug delivery.
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