Uptake of aluminum by lipid vesicles

Abstract

Aluminium uptake and tight binding were studied in multilayered phospholipid liposomes, as a model for cellular uptake of aluminum ions. Most of these studies were conducted with an initial aluminum concentration of 10 μM, while aluminum superficially bound to liposomes was removed by citrate chelation. Maximum uptake and tight binding of aluminium were pH‐dependent. In dimyristoyl phosphatidylcholine (DMPC) liposomes, this maximum occurred in the neutral pH region, while it was shifted towards more acidic pH values in DMPC liposomes containing 20% of acidic phosphatidylserine. The initial rate of aluminum uptake was apparently dependent on the physical state of the liposome membrane. Prior formation of an aluminum‐citrate chelate prevented aluminum uptake and tight binding to DMPC liposomes.