This work deals with the effect of Ca
2+ and La
3+ on the colloidal stability of phosphatidylcholine (PC)liposomes in aqueous media. As physical techniques, nephelometry, photon correlation spectroscopy,electrophoretic mobility, and surface tension were used. The theoretical predictions of the colloidal stabilityof liposomes were followed using the Derjaguin-Landau-Verwey-Overbeek theory. Changes in the sizeof liposomes and high polydispersity values were observed as La
3+ concentration increases, suggestingthat this cation induces the aggregation of liposomes. However, changes in polydispersity were not observedwith Ca
2+, suggesting a coalescence mechanism or fusion of liposomes. The stability factor (
W), calculatedfrom the nephelometry measurements indicated that aggregation/fusion occurs at a critical concentration(c.c.) of 0.3 and 0.7 M for La
3+ and Ca
2+, respectively. To gain a better insight into the interaction mechanismbetween the liposomes and the studied ions, the interaction between PC monolayers and Ca
2+ and La
3+was studied. Changes in the surface area per lipid molecule (
A0) in the monolayer at the c.c. values werefound for both ions, with a more pronounced effect in the case of Ca
2+. This corresponds with a largerreduction of the steric repulsive interaction between the headgroups at the phospholipid membrane (
head).The experimental result validates the hypothesis made on the liposome fusion in the presence of Ca
2+ andliposome aggregation in the presence of La
3+. These aggregation mechanisms have also been confirmedby transmission electron microscopy.