Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
10591108 | Bioorganic & Medicinal Chemistry Letters | 2014 | 6 Pages |
Abstract
Ferrocene-substituted porphyrin RL-91 exhibits antifungal activity against opportune human pathogen Candida albicans. RL-91 efficiently inhibits growth of both planktonic C. albicans cells and cells within biofilms without photoactivation. The minimal inhibitory concentration for plankton form (PMIC) was established to be 100 μg/mL and the same concentration killed 80% of sessile cells in the mature biofilm (SMIC80). Furthermore PMIC of RL-91 efficiently prevents C. albicans biofilm formation. RL-91 is cytotoxic for human fibroblasts in vitro in concentration of 10 μg/mL, however it does not cause hemolysis in concentrations of up to 50 μg/mL. These findings open possibility for application of RL-91 as an antifungal agent for external antibiofilm treatment of medical devices as well as a scaffold for further development of porphyrin based systemic antifungals.
Related Topics
Physical Sciences and Engineering
Chemistry
Organic Chemistry
Authors
Rainer Lippert, Sandra Vojnovic, Aleksandra Mitrovic, Norbert Jux, Ivana IvanoviÄ-BurmazoviÄ, Branka Vasiljevic, Nada Stankovic,