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Celecoxib-Loaded Cubosomal Nanoparticles as a Therapeutic Approach for Staphylococcus aureus In Vivo Infection.
Samar Zuhair Alshawwa1, Thanaa A El-Masry2, Mohamed Nasr3,4
1Department of Pharmaceutical Sciences, College of Pharmacy, Princess Nourah bint Abdulrahman University, P.O. Box 84428, Riyadh 11671, Saudi Arabia.
Novel cubosomal nanoparticles effectively deliver celecoxib to combat antibiotic-resistant Staphylococcus aureus infections. This nanotechnology enhances drug delivery, reducing bacterial load and inflammation in vivo.
Area of Science:
- Nanotechnology
- Pharmacology
- Microbiology
Background:
- Antibiotic resistance in bacteria like Staphylococcus aureus necessitates novel treatment strategies.
- Cubosomes offer a nanotechnology-based delivery system with potential for enhanced antibacterial action.
Purpose of the Study:
- To encapsulate celecoxib into cubosomal nanoparticles for improved antibacterial efficacy.
- To evaluate the in vitro characteristics and in vivo antibacterial activity of celecoxib-loaded cubosomes against Staphylococcus aureus.
Main Methods:
- Celecoxib encapsulation into cubosomes, followed by in vitro characterization (size, zeta potential, entrapment efficiency, release).
- In vivo assessment using a systemic infection model in mice, including tissue analysis (histopathology, immunostaining) and measurement of inflammatory markers.
Main Results:
- Celecoxib-loaded cubosomes exhibited favorable physicochemical properties (mean size 128.15 nm, negative zeta potential -17.50, entrapment efficiency 88.57%).
- In vivo studies demonstrated reduced bacterial burden, inflammation, and apoptosis in liver and spleen tissues of treated mice.
- Significant decrease in inflammatory markers (IL-1β, IL-6, COX-2, TNF-α) was observed, indicating effective modulation of inflammatory pathways.
Conclusions:
- Cubosomes represent a promising drug delivery system for celecoxib, enhancing its in vivo antibacterial activity.
- This formulation improves oral bioavailability and efficacy against Gram-positive bacterial infections.
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