Inhalable Polymeric Microparticles for Phage and Photothermal Synergistic Therapy of Methicillin-Resistant Staphylococcus aureus Pneumonia.
Meng-Yao LiuXing LiuChun-Yu WangQian-Qian WanYi-Fan TianShu-Lin LiuDai-Wen PangZhi-Gang WangPublished in: Nano letters (2024)
Acute methicillin-resistant Staphylococcus aureus (MRSA) pneumonia is a common and serious lung infection with high morbidity and mortality rates. Due to the increasing antibiotic resistance, toxicity, and pathogenicity of MRSA, there is an urgent need to explore effective antibacterial strategies. In this study, we developed a dry powder inhalable formulation which is composed of porous microspheres prepared from poly(lactic- co -glycolic acid) (PLGA), internally loaded with indocyanine green (ICG)-modified, heat-resistant phages that we screened for their high efficacy against MRSA. This formulation can deliver therapeutic doses of ICG-modified active phages to the deep lung tissue infection sites, avoiding rapid clearance by alveolar macrophages. Combined with the synergistic treatment of phage therapy and photothermal therapy, the formulation demonstrates potent bactericidal effects in acute MRSA pneumonia. With its long-term stability at room temperature and inhalable characteristics, this formulation has the potential to be a promising drug for the clinical treatment of MRSA pneumonia.
Keyphrases
- methicillin resistant staphylococcus aureus
- drug delivery
- cancer therapy
- respiratory failure
- staphylococcus aureus
- room temperature
- liver failure
- drug release
- pseudomonas aeruginosa
- drug induced
- escherichia coli
- fluorescence imaging
- stem cells
- community acquired pneumonia
- ionic liquid
- biofilm formation
- cystic fibrosis
- anti inflammatory
- photodynamic therapy
- oxidative stress
- mechanical ventilation
- mass spectrometry
- combination therapy
- mesenchymal stem cells
- risk assessment
- replacement therapy
- simultaneous determination
- smoking cessation
- molecularly imprinted
- tissue engineering