Matrix-Mediated Delivery of Silver Nanoparticles for Prevention of Staphylococcus aureus and Pseudomonas aeruginosa Biofilm Formation in Chronic Rhinosinusitis

Author:

Yathavan Bhuvanesh12,Chhibber Tanya12,Steinhauff Douglas23,Pulsipher Abigail124,Alt Jeremiah A.1234,Ghandehari Hamidreza1234,Jafari Paris125

Affiliation:

1. Department of Molecular Pharmaceutics, University of Utah, Salt Lake City, UT 84112, USA

2. Utah Center for Nanomedicine, University of Utah, Salt Lake City, UT 84112, USA

3. Department of Biomedical Engineering, University of Utah, Salt Lake City, UT 84112, USA

4. Department of Otolaryngology—Head and Neck Surgery, University of Utah School of Medicine, Salt Lake City, UT 84132, USA

5. Center for Integrative Genomics, University of Lausanne, 1015 Lausanne, Switzerland

Abstract

Chronic rhinosinusitis (CRS) is a chronic health condition affecting the sinonasal cavity. CRS-associated mucosal inflammation leads to sinonasal epithelial cell death and epithelial cell barrier disruption, which may result in recurrent bacterial infections and biofilm formation. For patients who fail medical management and elect endoscopic sinus surgery for disease control, bacterial biofilm formation is particularly detrimental, as it reduces the efficacy of surgical intervention. Effective treatments that prevent biofilm formation in post-operative patients in CRS are currently limited. To address this unmet need, we report the controlled release of silver nanoparticles (AgNps) with silk-elastinlike protein-based polymers (SELPs) to prevent bacterial biofilm formation in CRS. This polymeric network is liquid at room temperature and forms a hydrogel at body temperature, and is hence, capable of conforming to the sinonasal cavity upon administration. SELP hydrogels demonstrated sustained AgNp and silver ion release for the studied period of three days, potent in vitro antibacterial activity against Pseudomonas aeruginosa (**** p < 0.0001) and Staphylococcus aureus (**** p < 0.0001), two of the most commonly virulent bacterial strains observed in patients with post-operative CRS, and high cytocompatibility with human nasal epithelial cells. Antibacterial controlled release platform shows promise for treating patients suffering from prolonged sinonasal cavity infections due to biofilms.

Funder

Utah Clinical & Translational Science Institute

Skaggs Graduate Research Fellowship awarded by the University of Utah, College of Pharmacy

Research Incentive Seed Grant awarded by the University of Utah School of Medicine

National Center for Advancing Translational Sciences of the National Institutes of Health

Publisher

MDPI AG

Subject

Pharmaceutical Science

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