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Treatment of infection and inflammation associated with COVID-19, multi-drug resistant pneumonia and fungal sinusitis by nebulizing a nanosilver solution.
Nadworny, Patricia L; Hickerson, William L; Holley-Harrison, Holly Denise; Bloom, David C; Grams, Tristan R; Edwards, Terri G; Schultz, Gregory S; Burrell, Robert E.
  • Nadworny PL; Department of Biomedical Engineering, 1101 Research Transition Facility, University of Alberta, Edmonton, Alberta T6G 2V2, Canada; Department of Chemical and Materials Engineering, 9211 116 St. NW, University of Alberta, Edmonton, Alberta T6G 1H9, Canada. Electronic address: pnadworny@ualberta.ca.
  • Hickerson WL; Department of Plastic Surgery, 910 Madison Avenue, University of Tennessee Health Sciences Center, Memphis, TN 38163, USA. Electronic address: bhickerson@me.com.
  • Holley-Harrison HD; HNI Healthcare, Ascension Sacred Heart Hospital, 5151 N 9th Avenue, Pensacola, FL 32504, USA. Electronic address: hdeniseharrison@gmail.com.
  • Bloom DC; Department of Molecular Genetics and Microbiology, 1200 Newell Drive, University of Florida, Gainesville, FL 32610, USA. Electronic address: dbloom@ufl.edu.
  • Grams TR; Department of Molecular Genetics and Microbiology, 1200 Newell Drive, University of Florida, Gainesville, FL 32610, USA. Electronic address: tgrams@ufl.edu.
  • Edwards TG; Department of Molecular Genetics and Microbiology, 1200 Newell Drive, University of Florida, Gainesville, FL 32610, USA. Electronic address: tgedwards@ufl.edu.
  • Schultz GS; Institute for Wound Research, University of Florida, Gainsville, FL 32610, USA. Electronic address: schultzg@ufl.edu.
  • Burrell RE; Department of Biomedical Engineering, 1101 Research Transition Facility, University of Alberta, Edmonton, Alberta T6G 2V2, Canada; Department of Chemical and Materials Engineering, 9211 116 St. NW, University of Alberta, Edmonton, Alberta T6G 1H9, Canada. Electronic address: rburrell@ualberta.ca.
Nanomedicine ; 48: 102654, 2023 02.
Article in English | MEDLINE | ID: covidwho-2181759
ABSTRACT
Solutions containing Ag0 nanoclusters, Ag+1, and higher oxidation state silver, generated from nanocrystalline silver dressings, were anti-inflammatory against porcine skin inflammation. The dressings have clinically-demonstrated broad-spectrum antimicrobial activity, suggesting application of nanosilver solutions in treating pulmonary infection. Nanosilver solutions were tested for antimicrobial efficacy; against HSV-1 and SARS-CoV-2; and nebulized in rats with acute pneumonia. Patients with pneumonia (ventilated), fungal sinusitis, burns plus COVID-19, and two non-hospitalized patients with COVID-19 received nebulized nanosilver solution. Nanosilver solutions demonstrated pH-dependent antimicrobial efficacy; reduced infection and inflammation without evidence of lung toxicity in the rat model; and inactivated HSV-1 and SARS-CoV-2. Pneumonia patients had rapidly reduced pulmonary symptoms, recovering pre-illness respiratory function. Fungal sinusitis-related inflammation decreased immediately with infection clearance within 21 days. Non-hospitalized patients with COVID-19 experienced rapid symptom remission. Nanosilver solutions, due to anti-inflammatory, antiviral, and antimicrobial activity, may be effective for treating respiratory inflammation and infections caused by viruses and/or microbes.
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Full text: Available Collection: International databases Database: MEDLINE Main subject: Pneumonia / Sinusitis / COVID-19 Type of study: Prognostic study Topics: Long Covid Limits: Animals Language: English Journal: Nanomedicine Journal subject: Biotechnology Year: 2023 Document Type: Article

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Full text: Available Collection: International databases Database: MEDLINE Main subject: Pneumonia / Sinusitis / COVID-19 Type of study: Prognostic study Topics: Long Covid Limits: Animals Language: English Journal: Nanomedicine Journal subject: Biotechnology Year: 2023 Document Type: Article