Abstract
Objectives: E-101 Solution (E-101) is a novel myeloperoxidase-mediated antimicrobial. It is composed of porcine myeloperoxidase (pMPO), glucose oxidase, glucose as the substrate and specific amino acids in an aqueous vehicle. E-101 is being developed for topical application directly into surgical wounds to prevent surgical site infections (SSIs). The in vitro activity of E-101 was investigated. Methods: MIC, MBC, time-kill and antimicrobial combination experiments were performed according to CLSI guidelines with modifications. Resistance selection studies were performed using a serial passage method. Results: E-101 showed MIC90 values of 0.03, 0.5 and 0.5 mg pMPO/L for staphylococci (n=140), streptococci (n=95) and enterococci (n=55), respectively. MIC90 values ranged between 0.03-0.5 and ≤0.004-0.12 mg pMPO/L for Enterobacteriaceae (n=148) and Gram-negative non-Enterobacteriaceae (n=92) strains, respectively. There was no antimicrobial tolerance to E-101 for Staphylococcus aureus, Streptococcus agalactiae or Streptococcus pyogenes. Time-kill studies demonstrated a rapid (<30 min) bactericidal effect against S. aureus, Enterococcus faecalis, Escherichia coli and Pseudomonas aeruginosa in a concentration-dependent and time-dependent manner. There was no evidence of stable resistance to E-101 among staphylococci, enterococci, E. coli or P. aeruginosa strains and no evidence of E-101 interaction with antibiotics commonly used in clinical medicine. Conclusions: E-101 shows potent and broad-spectrum in vitro activity against bacteria that are the causative pathogens of SSIs, thereby providing the impetus to test its clinical utility in the prevention of SSIs. © The Author 2010. Published by Oxford University Press on behalf of the British Society for Antimicrobial Chemotherapy. All rights reserved.
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Denys, G. A., Grover, P., O’Hanley, P., & Stephens, J. T. (2011). In vitro antibacterial activity of E-101 solution, a novel myeloperoxidase-mediated antimicrobial, against Gram-positive and Gram-negative pathogens. Journal of Antimicrobial Chemotherapy, 66(2), 335–342. https://doi.org/10.1093/jac/dkq429
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