Original Article
Subject Category: Immunology/Infection
Journal of Investigative Dermatology (2009) 129, 2463–2469; doi:10.1038/jid.2009.95; published online 23 April 2009
Antimicrobial and Healing Efficacy of Sustained Release Nitric Oxide Nanoparticles Against Staphylococcus Aureus Skin Infection
Luis R Martinez1,2,6, George Han3,6, Manju Chacko3, Mircea Radu Mihu1,2, Marc Jacobson4,5, Phil Gialanella4, Adam J Friedman3,5,7, Joshua D Nosanchuk1,2,7 and Joel M Friedman3,7
- 1Division of Infectious Diseases, Departments of Medicine, Albert Einstein College of Medicine, Bronx, New York, USA
- 2Department of Microbiology and Immunology, Albert Einstein College of Medicine, Bronx, New York, USA
- 3Department of Physiology and Biophysics, Albert Einstein College of Medicine, Bronx, New York, USA
- 4Department of Pathology, Montefiore Medical Center, Bronx, New York, USA
- 5Division of Dermatology, Department of Medicine, Montefiore Medical Center, Bronx, New York, USA
Correspondence: Dr Joshua D. Nosanchuk, Department of Medicine, Albert Einstein College of Medicine, 1300 Morris Park Avenue, Bronx, New York 10461, USA. E-mail: nosanchu@aecom.yu.edu
6All these authors contributed equally to this work.
7These authors share senior authorship.
Received 3 November 2008; Revised 26 January 2009; Accepted 6 March 2009; Published online 23 April 2009.
Abstract
Staphylococcus aureus (SA) is a leading cause of both superficial and invasive infections in community and hospital settings, frequently resulting in chronic refractory disease. It is imperative that innovative therapeutics to which the bacteria are unlikely to evolve resistance be developed to curtail associated morbidity and mortality and ultimately improve our capacity to treat these infections. In this study, a previously unreported nitric oxide (NO)-releasing nanoparticle technology is applied to the treatment of methicillin-resistant SA (MRSA) wound infections. The results show that the nanoparticles exert antimicrobial activity against MRSA in a murine wound model. Acceleration of infected wound closure in NO-treated groups was clinically shown compared with controls. The histology of wounds revealed that NO nanoparticle treatment decreased suppurative inflammation, minimal bacterial burden, and less collagen degradation, providing potential mechanisms for biological activity. Together, these data suggest that these NO-releasing nanoparticles have the potential to serve as a novel class of topically applied antimicrobials for the treatment of cutaneous infections and wounds.
Abbreviations:
CFU, colony forming unit; MRSA, methicillin-resistant Staphylococcus aureus; MSSA, methicillin-sensitive Staphylococcus aureus; NO, nitric oxide; NO-np, nitric oxide through nanoparticle; PBS, phosphate-buffered saline



