Cited by 244Wound Healing and TreatmentsNanoparticles: synthesis and applicationsAntimicrobial Resistance in Staphylococcus

Antimicrobial and Healing Efficacy of Sustained Release Nitric Oxide Nanoparticles Against Staphylococcus Aureus Skin Infection

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Martinez, Luis R., Han, George, Chacko, Manju, Mihu, Mircea Radu, Jacobson, Marc, Gialanella, Phil, Friedman, Adam J., Nosanchuk, Joshua D. +1 more·2009·Journal of Investigative Dermatology

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.

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Crossref · 10.1038/jid.2009.95

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  • In murine skin infection models of S. aureus and MRSA biofilms, nitric oxide-releasing nanoparticles decreased overall wound bacterial burden compared with both unloaded nanoparticles and the control group.

    “In murine skin infection models of S. aureus and methicillin-resistant S. aureus biofilms, nitric oxide-releasing nanoparticles decreased overall wound bacterial burden compared with both unloaded nanoparticles and the control group 39 .”

    From Nanotechnology approaches for global infectious diseases (2021) · cites this paper as [39]

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References 17 · Cited by 244

Authors
Martinez, L. R., Han, G., Chacko, M., Mihu, M. R., Jacobson, M., Gialanella, P., Friedman, A. J., Nosanchuk, J. D., & Friedman, J. M.
Affiliations
  • Albert Einstein College of Medicine (US)
  • Montefiore Medical Center (US)
Corresponding author
Nosanchuk, Joshua D.
Venue
Journal of Investigative Dermatology
Publisher
Elsevier BV
Published
2009-10
Volume
129
Issue
10
Pages
2463-2469
ISSN
0022-202X (ISSN-L)
OpenAlex
W1982996309
Cited by
244
References
17
Citations by year
2026: 7 · 2025: 3 · 2024: 11 · 2023: 9 · 2022: 20 · 2021: 18 · 2020: 12 · 2019: 20 · 2018: 17 · 2017: 16 · 2016: 27 · 2015: 16 · 2014: 7 · 2013: 14 · 2012: 18
FWCI
15.62
Type
journal article
Language
en
Update notices
erratum (2010-03-01)
Open access
Locations
  • Journal of Investigative Dermatology (publishedVersion)
  • PubMed (publishedVersion)
Funders
  • National Institutes of Health (AI056070-01A2)
  • U.S. Department of Defense (DAMD17-03-1-0127)
Topics
  • Health Sciences › Medicine › Rehabilitation › Wound Healing and Treatments
  • Physical Sciences › Materials Science › Materials Chemistry › Nanoparticles: synthesis and applications
  • Health Sciences › Medicine › Infectious Diseases › Antimicrobial Resistance in Staphylococcus
Keywords
sustained drug release, methicillin-resistant Staphylococcus aureus, skin wound infection, topical antimicrobial agents, wound healing, suppurative inflammation, collagen degradation, skin infections, antibacterial activity
MeSH terms
Administration, Topical, Animals, Anti-Infective Agents, Biopsy, Collagen, Delayed-Action Preparations, Disease Models, Animal, Female, Mice, Inbred BALB C, Nitric Oxide, Skin, Staphylococcal Skin Infections, Wound Healing, Drug Delivery Systems, Treatment Outcome, Mice, Nanoparticles, Methicillin-Resistant Staphylococcus aureus

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