| Autor: |
Kassab G; São Carlos Institute of Physics, University of São Paulo, São Carlos, São Paulo 13566-590, Brazil., Diaz Tovar JS; São Carlos Institute of Physics, University of São Paulo, São Carlos, São Paulo 13566-590, Brazil., Souza LMP; Department of Chemistry, Pontifical Catholic University of Rio de Janeiro, Rio de Janeiro 22453-900, Brazil., Costa RKM; Department of Chemistry, Pontifical Catholic University of Rio de Janeiro, Rio de Janeiro 22453-900, Brazil., Silva RS; Department of Chemistry, Pontifical Catholic University of Rio de Janeiro, Rio de Janeiro 22453-900, Brazil., Pimentel AS; Department of Chemistry, Pontifical Catholic University of Rio de Janeiro, Rio de Janeiro 22453-900, Brazil., Kurachi C; São Carlos Institute of Physics, University of São Paulo, São Carlos, São Paulo 13566-590, Brazil., Bagnato VS; São Carlos Institute of Physics, University of São Paulo, São Carlos, São Paulo 13566-590, Brazil.; Hagler Institute for Advanced Studies, Texas A&M University, College Station, TX 77843. |
| Abstrakt: |
In the context of the rapid increase of antibiotic-resistant infections, in particular of pneumonia, antimicrobial photodynamic therapy (aPDT), the microbiological application of photodynamic therapy (PDT), comes in as a promising treatment alternative since the induced damage and resultant death are not dependent on a specific biomolecule or cellular pathway. The applicability of aPDT using the photosensitizer indocyanine green with infrared light has been successfully demonstrated for different bacterial agents in vitro, and the combination of pulmonary delivery using nebulization and external light activation has been shown to be feasible. However, there has been little progress in obtaining sufficient in vivo efficacy results. This study reports the lung surfactant as a significant suppressor of aPDT in the lungs. In vitro, the clinical surfactant Survanta® reduced the aPDT effect of indocyanine green, Photodithazine®, bacteriochlorin-trizma, and protoporphyrin IX against Streptococcus pneumoniae . The absorbance and fluorescence spectra, as well as the photobleaching profile, suggested that the decrease in efficacy is not a result of singlet oxygen quenching, while a molecular dynamics simulation showed an affinity for the polar head groups of the surfactant phospholipids that likely impacts uptake of the photosensitizers by the bacteria. Methylene blue is the exception, likely because its high water solubility confers a higher mobility when interacting with the surfactant layer. We propose that the interaction between lung surfactant and photosensitizer must be taken into account when developing pulmonary aPDT protocols. |
