Potential of ceragenin CSA-13 and its mixture with pluronic F-127 as treatment of topical bacterial infections.
Leszczyńska. K K; Namiot. A A; Cruz. K K; Byfield. F J FJ; Won. E E; Mendez. G G; Sokołowski. W W; Savage. P B PB; Bucki. R R; Janmey. P A PA
Key Findings
- CSA‑13 kills a broad range of bacteria, including MRSA and P. aeruginosa, in various body fluids
- Pluronic F‑127 preserves CSA‑13’s antibacterial activity but markedly reduces its haemolytic (red‑cell‑lysing) toxicity
- CSA‑13’s killing effect is enhanced by host defence molecules such as LL‑37, lysozyme, lactoferrin and sPLA
Practical Outcomes
- A topical formulation that combines CSA‑13 with pluronic F‑127 could provide strong antibacterial action with lower safety risks, making it a candidate for future skin‑infection creams. Adding or boosting LL‑37 may further improve efficacy, but the approach remains experimental and not yet ready for DIY use.
Summary
The study shows that the synthetic antibacterial molecule CSA-13 can kill tough skin germs like MRSA and Pseudomonas, even in body fluids, and that mixing it with the polymer pluronic F‑127 keeps its killing power while greatly lowering damage to red blood cells. It also works better when natural immune peptides like LL‑37 are present. While promising for a safer topical cream, the compound isn’t commercially available yet, so the findings are mostly useful as proof‑of‑concept for future DIY formulations.
Abstract
Ceragenin CSA-13 is a synthetic mimic of cationic antibacterial peptides, with facial amphiphilic morphology reproduced using a cholic acid scaffold. Previous data have shown that this molecule displays broad-spectrum antibacterial activity, which decreases in the presence of blood plasma. However, at higher concentrations, CSA-13 can cause lysis of erythrocytes. This study was designed to assess in vitro antibacterial and haemolytic activity of CSA-13 in the presence of pluronic F-127. CSA-13 bactericidal activity against clinical strains of bacteria associated with topical infections and in an experimental setting relevant to their pathophysiological environment, such as various epithelial tissue fluids and the airway sputum of patients suffering from cystic fibrosis (CF), was evaluated using minimum inhibitory and minimum bactericidal concentration (MIC/MBC) measurements and bacterial killing assays. We found that in the presence of pluronic F-127, CSA-13 antibacterial activity was only slightly decreased, but CSA-13 haemolytic activity was significantly inhibited. CSA-13 exhibits bacterial killing activity against clinical isolates of Staphylococcus aureus, including methicillin-resistant strains, Pseudomonas aeruginosa present in CF sputa, and biofilms formed by different Gram (+) and Gram (-) bacteria. CSA-13 bactericidal action is partially compromised in the presence of plasma, but is maintained in ascites, cerebrospinal fluid, saliva, and bronchoalveolar lavage fluid. The synergistic action of CSA-13, determined by the use of a standard checkerboard assay, reveals an increase in CSA-13 antibacterial activity in the presence of host defence molecules such as the cathelicidin LL-37 peptide, lysozyme, lactoferrin and secretory phospholipase A (sPLA). These results suggest that CSA-13 may be useful to prevent and treat topical infection. Combined application of CSA-13 with pluronic F-127 may be beneficial by reducing CSA-13 toxicity.
Study Information
pubmed
2010
2010-10-21T00:00:00.000Z
10.1111/j.1365-2672.2010.04874.x
59
47