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Complexation of phosphocholine liposomes with polylysine. Stabilization by surface coverage versus aggregation.
Dmitry Volodkin1, Vincent Ball, Pierre Schaaf
1Institut National de la Santé et de la Recherche Médicale, Unité 595, Faculté de Chirurgie Dentaire, 11 rue Humann, 67085 Strasbourg Cedex, France. Dmitry.Volodkin@medecine.u-strasbg.fr
Biochimica Et Biophysica Acta
|November 7, 2006
Summary
Complexation of poly-L-lysine (PLL) with liposomes can lead to charge inversion or aggregation. Controlling experimental conditions allows for tunable aggregation, forming stable colloids for applications like drug delivery.
Area of Science:
- Colloid and Surface Science
- Materials Science
- Biotechnology
Background:
- Liposomes are widely used as drug delivery vehicles.
- Polycations can interact with liposomes to modify their properties.
- Understanding these interactions is crucial for developing advanced delivery systems.
Purpose of the Study:
- To investigate the complexation between linear poly-L-lysine (PLL) and phosphocholine liposomes.
- To determine how experimental conditions influence complexation outcomes (charge inversion vs. aggregation).
- To explore the potential for controlling aggregate formation for specific applications.
Main Methods:
- Dynamic Light Scattering (DLS) for size analysis.
- Microelectrophoresis for surface charge determination.
- Differential Scanning Calorimetry (DSC) for thermal analysis.
Main Results:
- Complexation resulted in either charge inversion (stabilization) or aggregation, dependent on experimental variables.
- Aggregation was controllable, leading to the formation of stable, micron-sized aggregates.
- DSC confirmed physical adsorption on the vesicle surface without disturbing lipid organization.
Conclusions:
- The study elucidates multivariable aspects of liposome-polycation complexation.
- A procedure for fabricating polycation-stabilized vesicles was optimized.
- These findings support the development of novel colloidal systems for drug delivery.
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