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Updated: Jul 3, 2026

Microfluidic Production of Lysolipid-Containing Temperature-Sensitive Liposomes
Published on: March 3, 2020
Collisional solute release from thermally activated lipid particles
Pengyun Zeng1, Jeffrey Mahlberg, Timothy Scott Wiedmann
1Department of Pharmaceutics, University of Minnesota, Minneapolis, MN 55455, USA.
Solid lipid particles demonstrate potential as thermo-activated drug delivery systems. Drug release from these particles requires both micelles and heat, with release rates influenced by particle and micelle concentrations.
Area of Science:
- Materials Science
- Pharmaceutical Sciences
- Physical Chemistry
Background:
- Solid lipid particles (SLPs) are investigated for controlled drug delivery applications.
- Thermo-activated systems offer potential for targeted and on-demand drug release.
- Understanding release kinetics is crucial for optimizing drug delivery efficacy.
Purpose of the Study:
- To evaluate submicron-sized diphenylhexatriene (DPH)/myristyl alcohol solid lipid particles as a thermo-activated drug delivery system.
- To investigate the influence of micelle concentration and thermal activation on DPH release rates.
- To elucidate the mechanisms governing drug release from SLPs.
Main Methods:
- Submicron-sized DPH/myristyl alcohol particles were fabricated using an atomization/drying process.
- Drug release kinetics were measured by monitoring DPH release into sodium dodecyl sulfate (SDS) micellar solutions under varying conditions.
- A design study was employed to analyze the relationships between release rate, particle concentration, and micelle concentration.
Main Results:
- The release of DPH from SLPs was found to be dependent on both the presence of micelles and thermal activation.
- Initial DPH release rates were generally linear but showed nonlinearity at low micelle concentrations (rate decrease) and high particle/micelle concentrations (rate increase).
- Release rate was linearly proportional to particle concentration and nonlinearly related to micelle concentration, suggesting a saturable, possibly collision-based, release mechanism.
Conclusions:
- Solid lipid particles can function as thermo-activated drug delivery systems.
- Micelles and thermal energy are essential for DPH release, with release kinetics modulated by concentration-dependent factors.
- The findings suggest a saturable, collision-based mechanism for DPH release, providing insights for future drug delivery system design.
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