Multilayered vesicles prepared by reverse-phase evaporation: liposome structure and optimum solute entrapment
Liposome structure and solute entrapment in multilayered vesicles (MLVs) prepared by reverse-phase evaporation (REV) were studied. MLV-REV vesicles prepared from ether/water emulsions have high entrapment. Entrapment depends on drug, drug concentration, lipid, lipid concentration, and the container used to prepare the vesicles. By use of 300 /sup +/L of aqueous phase and 100 mg of phosphatidylcholine (PC), vesicles prepared in a test tube 25 mm x 175 mm have higher entrapment than vesicles prepared in a 100-mL round-bottom or pear-shaped flask. By use of a test tube, 100 mg of PC, and 300 ..mu..L of aqueous phase containing sucrose (1-50 mg/mL), >90% sucrose entrapment was obtained. Increasing lipid content to 150 mg of PC decreased entrapment to approx.80%. Neutral PC MLV-REV vesicles have optimum entrapment. Mixing negatively charged lipids or cholesterol (CH) with PC to make MLV-REV vesicles results in decreased entrapment compared to using only PC. Preparing vesicles with the solid lipid dipalmitoylphosphatidylcholine (DPPC) or DPPC/CH mixtures results in 30-40% entrapment when diethyl ether is used to make the MLV-REV emulsion. The high entrapment found for MLV vesicles prepared from water/organic solvent emulsions depends on maintaining a core during the process of liposome formation. A method to calculate the fraction of water residing in the liposomes' core is presented and used to compare multilayered vesicles prepared by different processes. X-ray diffraction data demonstrate that a heterogeneous distribution of lipid may exist in multilayered vesicles prepared by the REV process.
- Research Organization:
- Lilly Research Lab., Indianapolis, IN
- OSTI ID:
- 6789475
- Journal Information:
- Biochemistry; (United States), Journal Name: Biochemistry; (United States) Vol. 26:1; ISSN BICHA
- Country of Publication:
- United States
- Language:
- English
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Related Subjects
62 RADIOLOGY AND NUCLEAR MEDICINE
AQUEOUS SOLUTIONS
CELL CONSTITUENTS
CHOLESTEROL
COHERENT SCATTERING
DIFFRACTION
DISPERSIONS
ESTERS
EVAPORATION
HYDROXY COMPOUNDS
LIPIDS
LIPOSOMES
MIXTURES
MOLECULAR STRUCTURE
ORGANIC COMPOUNDS
ORGANIC PHOSPHORUS COMPOUNDS
ORGANOIDS
PHASE TRANSFORMATIONS
PHOSPHOLIPIDS
SCATTERING
SOLUTES
SOLUTIONS
STEROIDS
STEROLS
X-RAY DIFFRACTION