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Eur J Pharm Biopharm ; 160: 65-76, 2021 Mar.
Artículo en Inglés | MEDLINE | ID: mdl-33508436

RESUMEN

Biofilm mediated infection caused by multi-drug resistant bacteria are difficult to treat since it protects the microorganisms by host defense system, making them resistant to antibiotics and other antimicrobial agents. Combating such type of nosocomial infection, especially in immunocompromised patients, is an urgent need and foremost challenge faced by clinicians. Therefore, antimicrobial photodynamic therapy (aPDT) has been intensely pursued as an alternative therapy for bacterial infections. aPDT leads to the generation of reactive oxygen species (ROS) that destroy bacterial cells in the presence of a photosensitizer, visible light and oxygen. Here, we elucidated a possibility of its clinical application by reducing the treatment time and exposing curcumin to 20 J/cm2 of blue laser light, which corresponds to only 52 s to counteract vancomycin resistant Staphylococcus aureus (VRSA) both in vitro and in vivo. To understand the mechanism of action, the generation of total reactive oxygen species (ROS) was quantified by 2'-7'-dichlorofluorescein diacetate (DCFH-DA) and the type of phototoxicity was confirmed by fluorescence spectroscopic analysis. The data showed more production of singlet oxygen, indicating type-II phototoxicity. Different anti-biofilm assays (crystal violet and congo red assays) and microscopic studies were performed at sub-MIC concentration of curcumin followed by treatment with laser light against preformed biofilm of VRSA. The result showed significant reduction in the preformed biofilm formation. Finally, its therapeutic potential was validated in skin abrasion wistar rat model. The result showed significant inhibition of bacterial growth. Furthermore, immunomodulatory analysis with rat serum was performed. A significant reduction in expression of proinflammatory cytokines TNF-α and IL-6 were observed. Hence, we conclude that curcumin mediated aPDT with 20 J/cm2 of blue laser treatment (for 52 s) could be used against multi-drug resistant bacterial infections and preformed biofilm formation as a potential therapeutic approach.


Asunto(s)
Antiinfecciosos/administración & dosificación , Curcumina/administración & dosificación , Fotoquimioterapia/métodos , Infecciones Cutáneas Estafilocócicas/tratamiento farmacológico , Staphylococcus aureus Resistente a Vancomicina/efectos de los fármacos , Administración Cutánea , Animales , Carga Bacteriana/efectos de los fármacos , Carga Bacteriana/efectos de la radiación , Biopelículas/efectos de los fármacos , Biopelículas/crecimiento & desarrollo , Biopelículas/efectos de la radiación , Modelos Animales de Enfermedad , Farmacorresistencia Bacteriana Múltiple , Humanos , Láseres de Semiconductores , Masculino , Pruebas de Sensibilidad Microbiana , Fotoquimioterapia/instrumentación , Ratas , Especies Reactivas de Oxígeno/metabolismo , Piel/microbiología , Piel/patología , Infecciones Cutáneas Estafilocócicas/microbiología , Infecciones Cutáneas Estafilocócicas/patología , Staphylococcus aureus Resistente a Vancomicina/crecimiento & desarrollo , Staphylococcus aureus Resistente a Vancomicina/aislamiento & purificación
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