SIZE DISTRIBUTION OF SPONTANEOUSLY FORMED LIPOSOMES BY THE ALCOHOL INJECTION METHOD

ABSTRACT A dynamic light scattering study of the size distribution of POPC (1-palmitoyl-2-oleoyl-sn-glycero-3-phosphocholine) liposomes formed by the injection method is presented. By this method, an aliquot of methanol stock solution containing the surfactant is injected into water. The main aim of the present work was to determine under which conditions a monomodal and narrow size distribution could be obtained. The influence of several parameters on the size distribution was investigated. Firstly, we examined the influence of the POPC concentration in the initial stock methanol solution, when the POPC concentration in the final aqueous solution remains constant; secondly, the influence of POPC concentration in the aqueous phase, while the lipid concentration in the stock methanol remains constant. In both cases narrow monomodal size distributions of liposomes, centered between 40 and 70 nm, are obtained at low concentrations of POPC, in the stock methanol solution (≤25 mM) as well as in the final aqueous solution. However, at a higher lipid concentration range a more complex size distribution is observed, and an additional component larger than 500 nm is detected. The effect of dilution was also studied. It can be shown that dilution of the more concentrated POPC solutions determines the disappearance of the larger component, which is then ascribed to aggregates or clusters of smaller liposomes. Interestingly, by concentrating the diluted, monomodal liposomal suspensions, the monomodal distribution is maintained. Concentrated liposome preparations can therefore be obtained having only one population of liposomes centered around 40–70 nm radii. Finally, the effect of aging was studied. It appears that the larger components in the light scattering results are not time-stable, whereas the smaller liposome species are. It is shown that these features are also present when alcohols different from methanol are used.

[1]  Y. Maitani,et al.  MODIFIED ETHANOL INJECTION METHOD FOR LIPOSOMES CONTAINING β-SITOSTEROL β-D-GLUCOSIDE , 2001, Journal of liposome research.

[2]  M. Brandl,et al.  Liposomes with nifedipine and nifedipine-cyclodextrin complex: calorimetrical and plasma stability comparison , 1996 .

[3]  H. Döbereiner,et al.  Properties of giant vesicles , 2000 .

[4]  F. Szoka,et al.  Procedure for preparation of liposomes with large internal aqueous space and high capture by reverse-phase evaporation. , 1978, Proceedings of the National Academy of Sciences of the United States of America.

[5]  M. J. Campbell,et al.  Lipofection reagents prepared by a simple ethanol injection technique. , 1995, BioTechniques.

[6]  Miquel Pons,et al.  Liposomes obtained by the ethanol injection method , 1993 .

[7]  A. Bangham,et al.  Diffusion of univalent ions across the lamellae of swollen phospholipids. , 1965, Journal of molecular biology.

[8]  Y. Ishigami,et al.  Procedure for Preparation of Lipid Vesicles (Liposomes) Using the Coacervation (Phase Separation) Technique , 1995 .

[9]  P. Cullis,et al.  DIFFERENTIAL SCANNING MICROCALORIMETRIC STUDY OF VESICLES IN AQUEOUS-SOLUTIONS FORMED BY DIMETHYLDIOCTADECYLAMMONIUM BROMIDE , 1992 .

[10]  R. Wallace Is this a practical approach? , 2001, Journal of the American College of Surgeons.

[11]  R. New,et al.  Liposomes : a practical approach , 1990 .

[12]  N. Škalko-Basnet,et al.  Mucoadhesive chitosan-coated liposomes: characteristics and stability , 2001, Journal of microencapsulation.

[13]  J. Kremer,et al.  Vesicles of variable diameter prepared by a modified injection method. , 1977, Biochemistry.

[14]  H. Hauser,et al.  Spontaneous vesiculation of aqueous lipid dispersions. , 1986, Biochemistry.

[15]  L. Mayer,et al.  Vesicles of variable sizes produced by a rapid extrusion procedure. , 1986, Biochimica et biophysica acta.

[16]  Are Micelles and Vesicles Chemical Equilibrium Systems , 2001 .

[17]  E. Korn,et al.  Single bilayer liposomes prepared without sonication. , 1973, Biochimica et biophysica acta.

[18]  R. Naeff Feasibility of topical liposome drugs produced on an industrial scale , 1996 .

[19]  D. Lasič The spontaneous formation of unilamellar vesiscles , 1988 .

[20]  O Zumbuehl,et al.  Liposomes of controllable size in the range of 40 to 180 nm by defined dialysis of lipid/detergent mixed micelles. , 1981, Biochimica et biophysica acta.

[21]  W. Williams,et al.  A Simple Method for the Preparation of Liposomes for Pharmaceutical Applications: Characterization of the Liposomes , 1991, The Journal of pharmacy and pharmacology.