Anionic liposome formulation for oral delivery of thuricin CD, a potential antimicrobial peptide therapeutic
Loading...
Files
Published Version
Supplementary data
Date
2024
Authors
Journal Title
Journal ISSN
Volume Title
Publisher
Elsevier
Published Version
Abstract
Thuricin CD is a two-peptide antimicrobial produced by Bacillus thuringiensis. Unlike previous antibiotics, it has shown narrow spectrum activity against Clostridioides difficile, a bacterium capable of causing infectious disease in the colon. However, peptide antibiotics have stability, solubility, and permeability problems that can affect their performance in vivo. This work focuses on the bioactivity and bioavailability of thuricin CD with a view to developing a formulation for delivery of active thuricin CD peptides through the gastrointestinal tract (GIT) for local delivery in the colon. The results indicate that thuricin CD is active at low concentrations only when both peptides are present. While thuricin CD was degraded by proteases and was unstable and poorly soluble in gastric fluid, it showed increased solubility in intestinal fluid, probably due to micelle encapsulation. Based on this, thuricin CD was encapsulated in anionic liposomes, which showed increased activity compared to the free peptide, maintained activity after exposure to pepsin in gastric fluid and intestinal fluid, was stable in suspension for over 21 days at room temperature and for 60 days at 4 °C, and exhibited no toxicity to epithelial intestinal cells. These findings suggest that an anionic lipid-based nano formulation may be a promising approach for local oral delivery of thuricin CD.
Description
Keywords
Thuricin CD , Antimicrobial peptides , Bacteriocins , Antimicrobial resistance , Liposomes
Citation
Viera Herrera, C., O’Connor, P.M., Ratrey, P., Paul Ross, R., Hill, C. and Hudson, S.P. (2024) ‘Anionic liposome formulation for oral delivery of thuricin CD, a potential antimicrobial peptide therapeutic’, International Journal of Pharmaceutics, 654, 123918 (13pp). doi: 10.1016/j.ijpharm.2024.123918