Antimicrobial Photodynamic Therapy against Escherichia coli and Staphylococcus aureus Using Nanoemulsion-Encapsulated Zinc Phthalocyanine.
Nada T FelifelMahmoud A SliemZienat KamelJoanna BojarskaMohamed G SeadawyRehab M AminSherif M ElnagdyPublished in: Microorganisms (2023)
Multidrug-resistant microorganisms have become a significant public health threat, and traditional antibiotics are becoming ineffective. Photodynamic therapy (PDT) is a promising alternative that utilizes photosensitizers and light to produce Reactive Oxygen Species (ROS) that can kill microorganisms. Zinc phthalocyanine (ZnPc) is a promising photosensitizer due to its strong affinity for encapsulation in nanoemulsions and its antimicrobial properties. In this study, nanoemulsion was prepared using Miglyol 812N, a surfactant, and distilled water to dissolve hydrophobic drugs such as ZnPc. The nanoemulsion was characterized by its particle size, polydispersity index, Transmission Electron Microscope and Zeta potential, and the results showed that it was an efficient nanocarrier system that facilitated the solubilization of hydrophobic drugs in water. The use of ZnPc encapsulated in the nanoemulsion produced through the spontaneous emulsification method resulted in a significant reduction in cell survival percentages of gram-positive Staphylococcus aureus and gram-negative Escherichia coli by 85% and 75%, respectively. This may be attributed to the more complex cell membrane structure of E. coli compared to S. aureus . This demonstrates the potential of nanoemulsion-based PDT as an effective alternative to traditional antibiotics for treating multidrug-resistant microorganisms.
Keyphrases
- photodynamic therapy
- gram negative
- multidrug resistant
- staphylococcus aureus
- escherichia coli
- klebsiella pneumoniae
- reactive oxygen species
- drug resistant
- acinetobacter baumannii
- biofilm formation
- public health
- fluorescence imaging
- dna damage
- cell death
- human health
- mass spectrometry
- aqueous solution
- oxide nanoparticles
- drug induced
- cystic fibrosis
- risk assessment