Loading…

Hybrid bio-nanoporous peptide loaded-polymer platforms with anticancer and antibacterial activities

In this study, hybrid bio-nanoporous peptides loaded onto poly( N -isopropylacrylamide- co -butylacrylate) (pNIPAM- co -BA) coatings were designed and obtained via matrix-assisted pulsed laser evaporation (MAPLE) technique. The incorporation of cationic peptides magainin (MG) and melittin (Mel) and...

Full description

Saved in:
Bibliographic Details
Published in:Nanoscale advances 2024-04, Vol.6 (8), p.238-258
Main Authors: Icriverzi, Madalina, Florian, Paula Ecaterina, Bonciu, Anca, Dumitrescu, Luminita Nicoleta, Moldovan, Antoniu, Pelinescu, Diana, Ionescu, Robertina, Avram, Ionela, Munteanu, Cristian V. A, Sima, Livia Elena, Dinca, Valentina, Rusen, Laurentiu, Roseanu, Anca
Format: Article
Language:English
Subjects:
Citations: Items that this one cites
Online Access:Get full text
Tags: Add Tag
No Tags, Be the first to tag this record!
Description
Summary:In this study, hybrid bio-nanoporous peptides loaded onto poly( N -isopropylacrylamide- co -butylacrylate) (pNIPAM- co -BA) coatings were designed and obtained via matrix-assisted pulsed laser evaporation (MAPLE) technique. The incorporation of cationic peptides magainin (MG) and melittin (Mel) and their combination was tailored to target synergistic anticancer and antibacterial activities with low toxicity on normal mammalian cells. Atomic force microscopy, scanning electron microscopy, X-ray photoelectron spectroscopy, Fourier transform infrared spectroscopy as well as contact angle and surface energy measurements revealed the successful and functional incorporation of both the peptides within porous polymeric nanolayers as well as surface modifications ( i.e. variation in the pore size diameter, surface roughness, and wettability) after Mel, MG or Mel-MG incorporation compared to pNIPAM- co -BA. In vitro testing revealed the impairment of biofilm formation on all the hybrid coatings while testing with S. aureus , E. coli and P. aeruginosa . Moreover, MG was shown to modulate the effect of Mel in the combined Mel-MG extract formulation released via pNIPAM-platforms, thus significantly reducing cancer cell proliferation through apoptosis/necrosis as revealed by flow cytometry analysis performed in vitro on HEK293T, A375, B16F1 and B16F10 cells. To the best of our knowledge, Mel-MG combination entrapped in the pNIPAM- co -BA copolymer has not yet been reported as a new promising candidate with anticancer and antibacterial properties for improved utility in the biomedical field. Mel-MG incorporation compared to pNIPAM- co -BA in in vitro testing revealed the impairment of biofilm formation in all the hybrid formulations. pNIPAM- co -BA coatings featuring nanopore biointerfaces obtained vis laser methods incorporating magainin/melittin peptides impair bacterial growth and reduce cancer cell proliferation.
ISSN:2516-0230
2516-0230
DOI:10.1039/d3na00947e