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Calcein release from temperature-sensitive liposome with or without stirring
A Ono1, M Yamaguchi, I Horikoshi
1Department of Hospital Pharmacy, Toyama Medical and Pharmaceutical University, Sugitani, Japan.
Biological & Pharmaceutical Bulletin
|January 1, 1994
Summary
Stirring temperature-sensitive liposomes (liposomes) reduces the temperature required for calcein release by 8 degrees Celsius. Mixed liposomes showed maximum release near 40-45°C, depending on stirring.
Area of Science:
- Liposome research
- Drug delivery systems
- Physical chemistry
Background:
- Temperature-sensitive liposomes are crucial for controlled drug release.
- Understanding factors affecting liposome release kinetics is essential for optimizing therapeutic applications.
- Liposome composition and environmental conditions significantly influence drug release profiles.
Purpose of the Study:
- To investigate the effect of stirring on calcein release from dipalmitoylphosphatidylcholine (DPPC) liposomes.
- To determine the optimal temperature for maximum calcein release from mixed DPPC-distearoylphosphatidylcholine (DSPC) liposomes under different stirring conditions.
Main Methods:
- Utilized reverse phase evaporation vesicle (REV) technology to create liposomes.
- Incorporated the fluorescent marker calcein into liposomes.
- Measured calcein release rates at various temperatures with and without mechanical stirring.
Main Results:
- Stirring decreased the temperature required for calcein release from DPPC REVs by approximately 8°C.
- DPPC-DSPC mixed REVs exhibited maximum calcein release around 40°C with stirring.
- Maximum release for mixed REVs without stirring was observed near 45°C.
Conclusions:
- Stirring significantly alters the thermal transition and release characteristics of temperature-sensitive liposomes.
- Liposome composition, specifically the inclusion of DSPC, can modulate the release temperature.
- These findings provide valuable insights for designing advanced liposomal drug delivery systems with tunable release profiles.