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.

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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