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Studies on molecular interactions between nalidixic acid and liposomes
1Institute of Biophysics and Radiation Biology, Faculty of Medicine, Semmelweis University, Budapest VIII, P.O. Box 263, Puskin u. 9, H-1444 Budapest, Hungary.
International Journal of Pharmaceutics
|July 6, 2004
Summary
Nalidixic acid sodium salt interacts with liposome lipid head groups. Ultraviolet-B light exposure causes free radical formation, affecting liposome properties and phase transitions, especially with dioleoyl-phosphatidylcholine content.
Area of Science:
- Lipid-drug interactions
- Photochemistry
- Nanomedicine
Background:
- Liposomes are crucial drug delivery systems.
- Nalidixic acid sodium salt (NANa) is an antibiotic.
- Understanding drug-liposome interactions is vital for effective drug delivery.
Purpose of the Study:
- To investigate the interaction between NANa and liposomes composed of DPPC and DOPC.
- To evaluate the impact of UV-B irradiation on these interactions and radical formation.
- To characterize liposome stability and phase transition modifications.
Main Methods:
- Differential scanning calorimetry (DSC) for thermal analysis.
- Electron paramagnetic resonance (EPR) spectroscopy for molecular interactions and radical kinetics.
- Dynamic light scattering (DLS) for liposome size distribution.
- Spectrophotometry for entrapment efficiency determination.
Main Results:
- NANa primarily interacts with the head groups of liposome lipids.
- UV-B irradiation induces free radical formation, with effects extending beyond the head group region.
- Liposome phase transition parameters are altered by NANa, influenced by the dioleoyl-phosphatidylcholine content.
Conclusions:
- NANa interacts with liposome lipid head groups, and UV-B irradiation induces free radicals.
- The observed effects on liposome properties are dependent on lipid composition, particularly DOPC content.
- These findings provide insights into the stability and behavior of NANa-loaded liposomes under UV-B exposure.