Affiliations 

  • 1 Department of Pathobiology and Population Science, Royal Veterinary College, University of London, Royal College Street, London NW1 0TU, UK. [email protected]
  • 2 University College London School of Pharmacy, 29-39 Brunswick Square, Bloomsbury, London WC1N 1AX, UK. [email protected]
  • 3 UCL Centre for Nanotechnology and Regenerative Medicine, Division of Surgery & Interventional Science, University College London, London NW3 2PF, UK. [email protected]
  • 4 Department of Pathobiology and Population Science, Royal Veterinary College, University of London, Royal College Street, London NW1 0TU, UK. [email protected]
Polymers (Basel), 2018 May 12;10(5).
PMID: 30966555 DOI: 10.3390/polym10050521

Abstract

The treatment of skin and soft tissue infections caused by methicillin-resistant Staphylococcus aureus (MRSA) remains a challenge, partly due to localization of the bacteria inside the host's cells, where antimicrobial penetration and efficacy is limited. We formulated the cationic polymer polyhexamethylene biguanide (PHMB) with the topical antibiotic nadifloxacin and tested the activities against intracellular MRSA in infected keratinocytes. The PHMB/nadifloxacin nanoparticles displayed a size of 291.3 ± 89.6 nm, polydispersity index of 0.35 ± 0.04, zeta potential of +20.2 ± 4.8 mV, and drug encapsulation efficiency of 58.25 ± 3.4%. The nanoparticles killed intracellular MRSA, and relative to free polymer or drugs used separately or together, the nanoparticles displayed reduced toxicity and improved host cell recovery. Together, these findings show that PHMB/nadifloxacin nanoparticles are effective against intracellular bacteria and could be further developed for the treatment of skin and soft tissue infections.

* Title and MeSH Headings from MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine.