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Bactericidal Activity of Lipid-Shelled Nitric Oxide-Loaded Microbubbles
Maxime Lafond1, Himanshu Shekhar1, Warunya Panmanee2
1Department of Internal Medicine, Division of Cardiovascular Health and Disease, University of Cincinnati, Cincinnati, OH, United States.
Nitric oxide (NO)-loaded microbubbles enhance antibacterial therapy against resistant bacteria. Co-encapsulating NO with octafluoropropane improves NO delivery and efficacy, showing promise for treating infections.
Area of Science:
- Biomedical Engineering
- Nanotechnology
- Infectious Diseases
Background:
- Antibiotic resistance is a growing global health crisis, necessitating novel therapeutic strategies.
- Nitric oxide (NO) possesses potent bactericidal and anti-biofilm properties, but its therapeutic application is limited by its instability.
- Microbubbles (MB) offer a potential platform for controlled delivery of therapeutic agents like NO.
Purpose of the Study:
- To characterize nitric oxide-loaded microbubbles (NO-MB) stabilized with a lipid shell.
- To evaluate the feasibility of using these NO-MB for *in vitro* antibacterial therapy.
- To assess the impact of co-encapsulating NO with octafluoropropane (OFP) on MB properties and efficacy.
Main Methods:
- NO-MB and NO-OFP-MB were prepared and characterized for size distribution and acoustic attenuation.
- Ultrasound was used to trigger gas payload release, and NO concentration was measured using an amperometric sensor.
- The bactericidal efficacy against *Staphylococcus aureus* (SA) USA 300 was assessed *in vitro*.
Main Results:
- Co-encapsulation of NO with OFP increased MB volume and acoustic attenuation.
- Ultrasound successfully triggered gas release from NO-OFP-MB, delivering higher NO concentrations than saturated solutions.
- NO-OFP-MB demonstrated enhanced bactericidal efficacy against *S. aureus* compared to control groups.
Conclusions:
- Encapsulating NO with OFP in lipid-shelled MB improves NO payload delivery and enhances antibacterial efficacy.
- NO-OFP-MB show feasibility for antibacterial applications, with potential for treating resistant infections.
- Further studies are needed to explore the limitations and optimize NO-OFP-MB for clinical translation.
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