Antimicrobial peptides (AMPs) are promising alternatives to conventional
antibiotics and
chemotherapy in the treatment of multidrug-resistant pathogens and
drug-resistant
cancers. Clinical application of AMPs is limited due to low stability and inefficient transport. Encapsulation in nanocarriers may improve their therapeutic potential.
Chitosan nanoparticles (CS-NPs) are efficient carriers for
proteins and
peptides, improving the treatment of microbial
infections and targeted
drug delivery. We examined toxicity against
cancer cell lines and antibacterial activities of the
pleurocidin-like
AMP NRC-07 upon encapsulation in CS-NPs by ionotropic gelation. The
biological activities of various formulations of free and encapsulated NRC-07 and free nanoparticles were evaluated against Pseudomonas aeruginosa and
breast cancer cells, using assays for cell viability and
lactate dehydrogenase cytolysis with non-
cancer cell lines as controls. NRC-07-containing nanoparticles decreased the bacterial and
cancer cell viability in a concentration-dependent manner. Activities of encapsulated
peptide were >2-fold higher than those of free NRC-07
peptide. Unloaded CS-NPs and free
peptide were not cytotoxic against control cells. Encapsulation of NRC-07 into CS-NPs enhanced the antibacterial and selective cytotoxicity of the
peptide, possibly enhancing anticancer activities. Encapsulation presents a promising tool for the development of efficient drug delivery systems.