A Topical Hydrogel with Deferiprone and Gallium-Protoporphyrin Targets Bacterial Iron Metabolism and Has Antibiofilm Activity

Many infectious diseases are associated with multidrug-resistant (MDR) bacteria residing in biofilms that require high antibiotic concentrations. While oral drug delivery is frequently ineffective, topical treatments have the potential to deliver higher drug concentrations to the infection site whil...

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Veröffentlicht in:Antimicrobial agents and chemotherapy 2017-06, Vol.61 (6)
Hauptverfasser: Richter, Katharina, Thomas, Nicky, Claeys, Jolien, McGuane, Jonathan, Prestidge, Clive A, Coenye, Tom, Wormald, Peter-John, Vreugde, Sarah
Format: Artikel
Sprache:eng
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Zusammenfassung:Many infectious diseases are associated with multidrug-resistant (MDR) bacteria residing in biofilms that require high antibiotic concentrations. While oral drug delivery is frequently ineffective, topical treatments have the potential to deliver higher drug concentrations to the infection site while reducing systemic side effects. This study determined the antibiofilm activity of a surgical wound gel loaded with the iron chelator deferiprone (Def) and the heme analogue gallium-protoporphyrin (GaPP), alone and in combination with ciprofloxacin. Activity against MDR , , , and biofilms was assessed in the colony biofilm and artificial wound model by enumeration of CFU and correlative light/electron microscopy. While biofilms were equally susceptible to GaPP and Def-GaPP gels (log reduction of 3.8 and 3.7, respectively), the Def-GaPP combination was crucial for significant activity against biofilms (log reduction of 1.3 for GaPP and 3.3 for Def-GaPP). When Def-GaPP gel was combined with ciprofloxacin, the efficacy exceeded the activity of the individual compounds. Def-GaPP delivered in a surgical wound gel showed significant antibiofilm activity against different MDR strains and could enhance the gel's wound-healing properties. Moreover, Def-GaPP indicated a potentiation of ciprofloxacin. This antibiofilm strategy has potential for clinical utilization as a therapy for topical biofilm-related infections.
ISSN:0066-4804
1098-6596
DOI:10.1128/AAC.00481-17