Poly-(lactic- co -glycolic) Acid Nanoparticles Entrapping Pterostilbene for Targeting Aspergillus Section Nigri .
Anastasia OrekhovaCleofe PalocciLaura ChronopoulouGiulia De AngelisCamilla BadialiValerio PetruccelliSimone D'AngeliGabriella PasquaGiovanna SimonettiPublished in: Molecules (Basel, Switzerland) (2022)
Poly-(lactic- co -glycolic) acid (PLGA) is a biodegradable, biosafe, and biocompatible copolymer. The Aspergillus section Nigri causes otomycosis localized in the external auditory canal. In this research, Aspergillus brasiliensis , a species belonging to the Nigri section, was tested. Coumarin 6 and pterostilbene loaded in poly-(lactic- co -glycolic) acid nanoparticles (PLGA-coumarin6-NPs and PLGA-PTB-NPs) were tested for fungal cell uptake and antifungal ability against A. brasiliensis biofilm, respectively. Moreover, the activity of PLGA-PTB-NPs in inhibiting the A. brasiliensis infection was tested using Galleria mellonella larvae. The results showed a fluorescence signal, after 50 nm PLGA-coumarin6-NPs treatment, inside A. brasiliensis hyphae and along the entire thickness of the biofilm matrix, which was indicative of an efficient NP uptake. Regarding antifungal activity, a reduction in A. brasiliensis biofilm formation and mature biofilm with PLGA-PTB-NPs has been demonstrated. Moreover, in vivo experiments showed a significant reduction in mortality of infected larvae after injection of PLGA-PTB-NPs compared to free PTB at the same concentration. In conclusion, the PLGA-NPs system can increase the bioavailability of PTB in Aspergillus section Nigri biofilm by overcoming the biofilm matrix barrier and delivering PTB to fungal cells.
Keyphrases
- drug delivery
- biofilm formation
- drug release
- candida albicans
- pseudomonas aeruginosa
- staphylococcus aureus
- cancer therapy
- bone regeneration
- oxide nanoparticles
- escherichia coli
- cell wall
- fluorescent probe
- cystic fibrosis
- stem cells
- induced apoptosis
- optical coherence tomography
- cardiovascular disease
- type diabetes
- coronary artery disease
- photodynamic therapy
- single molecule
- cell death
- cell proliferation
- risk factors
- working memory
- oxidative stress
- mesenchymal stem cells
- genetic diversity
- combination therapy
- bone marrow