Abstract
An attempt has been made to design suitable niosome-encapsulated drug delivery system for ciprofloxacin and norfloxacin. Encapsulation of ciprofloxacin and norfloxacin in niosomes was investigated and the nasal and intestinal absorption of the products studied. More than 80% of the drugs were successfully encapsulated to give products with sustained release characteristics. Encapsulation in niosomes also improved the stability of the antibacterial compounds. Although the systemic availability of these niosome-encapsulated antibacterial compounds was not increased after nasal administration, intestinal absorption was significantly higher in comparison with that of plain inclusion complexes.
Original language | English |
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Pages (from-to) | 145-149 |
Number of pages | 5 |
Journal | Journal of Pharmacy and Pharmacology |
Volume | 49 |
Issue number | 2 |
Publication status | Published - 02-1997 |
All Science Journal Classification (ASJC) codes
- Pharmacology
- Pharmaceutical Science