Effect of C7-3-Peptide-Loaded Chitosan Nanoparticles Against Multi-Drug-Resistant Neisseria gonorrhoeae .
Asma Ismail AlbdrawyFadilah Sfouq AleanizyEsraa Kamal EltaybAbdullah A AldossariMohammed M AlanaziRihaf AlfarajEram Kd EltahirHibah M AlbasriJouri S AlanaziFulwah Yahya AlqahtaniPublished in: International journal of nanomedicine (2024)
All prepared NPs were optimized for the smallest particle size of 136.9 to 168.3 nm. The EE% of C7-3, C7-3m1, and C7-3m2 CNPs reached 90.2, 92.5, and 91.8%, respectively. An in vitro release study demonstrated a continuous sustained-release pattern of C7-3 peptide from NPs. The SDS-PAGE assay confirmed the integrity of C7-3 peptide after the fabrication process. When comparing each peptide alone, the generated NPs demonstrated higher anti-gonococcal and anti-biofilm effectiveness against standard and resistant bacterial strains under anaerobic conditions. The cytotoxicity experiments revealed the cytocompatibility of NPs in HeLa cell lines. Given the advantages of enhanced anti-gonococcal activity of the C7-3 peptide and its derivatives when loaded with CNPs, as well as the antimicrobial properties of chitosan NPs, the reported NPs have great potential in the treatment of gonococcal infection.
Keyphrases
- drug resistant
- drug delivery
- oxide nanoparticles
- multidrug resistant
- staphylococcus aureus
- wound healing
- systematic review
- escherichia coli
- acinetobacter baumannii
- cancer therapy
- microbial community
- photodynamic therapy
- single cell
- candida albicans
- signaling pathway
- climate change
- hyaluronic acid
- combination therapy
- biofilm formation
- tissue engineering