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Published on: February 9, 2019
Azithromycin cationic non-lecithoid nano/microparticles improve bioavailability and targeting efficiency.
Meng Zhong1, Yue Feng, Hong Liao
1Medicine Engineering Research Center, Chongqing Medical University, Chongqing, 400016, People's Republic of China.
This study developed novel azithromycin cationic non-lecithoid nano/microparticles, demonstrating significantly enhanced oral and intravenous bioavailability and improved lung targeting efficiency for azithromycin delivery.
Area of Science:
- Nanotechnology
- Pharmaceutical Sciences
- Drug Delivery Systems
Background:
- Azithromycin is a widely used antibiotic.
- Current drug delivery methods for azithromycin have limitations in bioavailability and targeted delivery.
- Niosomes offer a promising non-lecithoid alternative for drug encapsulation.
Purpose of the Study:
- To develop and evaluate azithromycin cationic non-lecithoid nano/microparticles (AMCNS).
- To achieve high bioavailability and efficient lung targeting of azithromycin.
- To explore oral and intravenous administration routes for AMCNS.
Main Methods:
- Cationic niosomes of varying sizes (AMCNS-S and AMCNS-L) were synthesized.
- Azithromycin (AM) was encapsulated within the niosomes.
- Bioavailability and lung targeting efficiency were assessed after oral and intravenous administration in comparison to free AM.
Main Results:
- AMCNS exhibited significantly enhanced oral (up to 273.19%) and intravenous (up to 163.50%) relative bioavailability compared to free AM.
- Intravenous administration of AMCNS resulted in substantial lung targeting efficiency, with lung AM concentrations 16-28 times higher than free AM at 12 hours.
- Consistent higher AM concentrations in the lungs compared to heart and kidney were observed with AMCNS.
Conclusions:
- Niosome-based azithromycin nanocarriers (AMCNS) demonstrate high bioavailability and effective lung targeting.
- This development offers a valuable strategy for antibacterial therapy using non-lecithoid niosomal applications.
- The study highlights the potential of AMCNS for improved azithromycin delivery.
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