Azithromycin-loaded liposomal hydrogel: a step forward for enhanced treatment of MRSA-related skin infections

Zora Rukavina1, May Wenche Jøraholmen2, Dunja Božić3

  • 11Department of Pharmaceutical Technology, University of Zagreb Faculty of Pharmacy and Biochemistry, 10000 Zagreb, Croatia.

PubMed

Insights

This study explored combining azithromycin (AZT) liposomes with chitosan hydrogel (CHG) for enhanced topical treatment of methicillin-resistant Staphylococcus aureus (MRSA) skin infections. The cationic liposomal CHG formulation demonstrated superior anti-MRSA activity and biocompatibility.

Area of Science:

  • Pharmaceutics
  • Dermatology
  • Infectious Diseases

Background:

  • Azithromycin (AZT)-loaded liposomes show in vitro activity against methicillin-resistant Staphylococcus aureus (MRSA).
  • Localized treatment of MRSA skin infections requires formulations with enhanced therapeutic potential.
  • Chitosan hydrogel (CHG) can modify drug release and improve formulation properties.

Purpose of the Study:

  • To evaluate the anti-MRSA potential of azithromycin liposomes incorporated into chitosan hydrogel (liposomal CHGs) for localized topical treatment.
  • To assess the impact of CHG incorporation on AZT release, viscosity, texture, and antibacterial activity.
  • To identify the most promising liposomal CHG formulation for MRSA skin infections.

Main Methods:

  • Preparation and evaluation of four different liposomal CHG formulations.
  • Assessment of antibacterial activity against MRSA.
  • Analysis of AZT release profiles, cytotoxicity, texture, and rheological properties.

Main Results:

  • Chitosan hydrogel provided suitable viscoelastic and texture properties for prolonged AZT retention and release.
  • Liposomal CHGs demonstrated boosted anti-MRSA effects compared to AZT-liposomes alone.
  • The cationic liposomal CHG formulation (CATL-CHG) exhibited the most promising anti-MRSA activity and biocompatibility.

Conclusions:

  • Liposomal CHGs are a promising strategy for the topical treatment of MRSA-related skin infections.
  • CHG enhances the therapeutic potential of AZT-liposomes through controlled release and improved formulation characteristics.
  • CATL-CHG is identified as the leading candidate for further development in treating MRSA skin infections.

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