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Author Spotlight: Exploring the Antibacterial Effects of Zinc Oxide Nanoparticles in Overcoming Antibiotic Resistance
Published on: September 27, 2024
Characterization and application of roxithromycin loaded cyclodextrin based nanoparticles for treatment of multidrug
Farha Masood1, Tariq Yasin2, Habib Bukhari1
1Department of Biosciences, COMSATS Institute of Information Technology (CIIT), Islamabad, Pakistan.
Abstract:
An outbreak of infections with a high mortality rate caused by multidrug resistant (MDR) bacteria is one of the biggest health challenges globally. A class IV drug, roxithromycin (ROX), has poor solubility. In this study, ROX was first encapsulated in the cavity of each of the β-cyclodextrin (βCD) and hydroxypropyl-β-cyclodextrin (HPβCD). Then, each of the resulting βCD-ROX inclusion complex and HPβCD-ROX inclusion complex were separately loaded into poly-(lactic-co-glycolic acid) (PLGA) to synthesize βCD-ROX/PLGA and HPβCD-ROX/PLGA nanoparticles (NPs). Blank and ROX loaded PLGA (ROX-PLGA) NPs were also prepared. The loading efficiency of ROX is comparatively high for HPβCD-ROX/PLGA NPs in comparison to the βCD-ROX/PLGA NPs and ROX-PLGA NPs. All designed formulations showed significant (P<0.0001) antibacterial activity against the selected MDR bacterial strains. In a nutshell, this study demonstrated a great therapeutic potential of the above-mentioned delivery systems for treatment of MDR bacteria.
Insights
This study developed novel nanoparticles for roxithromycin (ROX) to combat multidrug-resistant (MDR) bacteria. The hydroxypropyl-β-cyclodextrin (HPβCD)-ROX/PLGA nanoparticles demonstrated significant antibacterial activity against MDR strains.
Area of Science:
- Pharmaceutical Nanotechnology
- Drug Delivery Systems
- Antimicrobial Resistance
Background:
- Multidrug-resistant (MDR) bacterial infections pose a significant global health threat.
- Roxithromycin (ROX), a class IV antibiotic, suffers from poor solubility, limiting its therapeutic efficacy.
- Effective drug delivery systems are crucial for overcoming challenges associated with MDR infections.
Purpose of the Study:
- To develop and characterize novel nanoparticle formulations for enhanced delivery of roxithromycin (ROX).
- To improve the solubility and therapeutic potential of ROX against multidrug-resistant (MDR) bacteria.
- To evaluate the antibacterial activity of ROX-loaded nanoparticles against selected MDR bacterial strains.
Main Methods:
- Encapsulation of roxithromycin (ROX) within β-cyclodextrin (βCD) and hydroxypropyl-β-cyclodextrin (HPβCD).
- Loading of ROX-cyclodextrin inclusion complexes into poly-(lactic-co-glycolic acid) (PLGA) to form nanoparticles (NPs).
- Preparation of blank and ROX-loaded PLGA nanoparticles for comparison.
Main Results:
- Hydroxypropyl-β-cyclodextrin-ROX/PLGA (HPβCD-ROX/PLGA) nanoparticles exhibited higher ROX loading efficiency compared to other formulations.
- All synthesized nanoparticle formulations demonstrated significant (P<0.0001) antibacterial activity against MDR bacterial strains.
- The developed nanoparticle systems showed promising results in enhancing ROX delivery.
Conclusions:
- HPβCD-ROX/PLGA nanoparticles represent a promising strategy for improving roxithromycin solubility and delivery.
- These novel delivery systems hold significant therapeutic potential for combating infections caused by multidrug-resistant bacteria.
- Further research into these nanocarriers could lead to advanced treatments for antimicrobial resistance.
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