Layer-by-layer assembled melanin nanoparticles thin films for photodynamic activity-based disinfection by ultraviolet A irradiation

  • Egemen Umur
  • , Fahriye Arslan
  • , Emel Bakay
  • , Busra Sirek
  • , Bugra Ayan*
  • , Engin Baysoy
  • , Nermin Topaloğlu
  • , Gizem Kaleli-Can*
  • *Korresponderande författare för detta arbete

Forskningsoutput: TidskriftsbidragArtikelVetenskapligPeer review

3 Citeringar (Scopus)

Sammanfattning

Hospitalized patients with indwelling catheters face the threat of catheter-associated infections (CAIs), which often lead to high morbidity and mortality rates. Disinfection procedures including metal-based antibacterial coatings and photosensitive nanoparticles are unsatisfactory due to concerns associated with long-term toxicity. This study investigates photodynamic capabilities of natural melanin nanoparticles (MNPs) as a layer-by-layer assembled (LBL-A) MNPs thin film to avoid biofilm formation and reveals the physical–chemical properties of LBL-A MNPs thin film using Scanning Electron Microscopy (SEM), Attenuated Total Reflectance-Fourier Transform Infrared (ATR-FTIR) spectroscopy, UV–visible spectroscopy, and ability to generate reactive oxygen species (ROS). Additionally, the biocompatibility of LBL-A MNPs thin films in terms of their cytotoxic effect on fibroblast cells was examined. The highest cellular inactivation rates for E. coli bacteria with 86.7% and S. aureus with 80.5% were achieved when the developed LBL-A MNP thin films were exposed to UV-A irradiation (395–400 nm) for 60 s with a distance of 1 cm. In contrast, The LBL-A MNPs thin film protected fibroblast cells against UV-A irradiation with no significant reduction in cell viability. In this regard, the MNPs-based photodynamic method not only enables the treatment of CAIs within only 60 s of UV-A irradiation, but also eliminates the harmful effects of both UV-C and metal-based nanoparticles in living organisms.

OriginalspråkEngelska
Sidor (från-till)2547-2562
Antal sidor16
TidskriftEmergent Materials
Volym7
Nummer6
DOI
StatusPublicerad - dec. 2024
MoE-publikationstypA1 Tidskriftsartikel-refererad

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