T. Nishiya et al., MECHANISTIC STUDY ON TOXICITY OF POSITIVELY CHARGED LIPOSOMES CONTAINING STEARYLAMINE TO BLOOD, Artificial cells, blood substitutes, and immobilization biotechnology, 23(4), 1995, pp. 505-512
We studied the interaction of stearylamine (SA) containing liposomes (
SA-liposomes) with erythrocyte ghost (EG) or platelets, utilizing the
Tb/dipicolinate (Tb/DPA) assay for the mixing of aqueous contents and
a resonance energy transfer (RET) assay for the mixing of lipid. The r
esults demonstrate that SA-liposomes and EG, after aggregation, have a
great tendency to mix their lipid before the mixing of the internal c
ontents. The mixing of their contents takes place inside the vesicles
due to the fusion of SA-liposomes and EG, followed by the leakage of t
he contents from the vesicles. In the presence of carboxymethyl chitin
(CM-chitin), SA-liposomes-EG interaction was inhibited indicating tha
t CM-chitin reduces the tendency bf SA-liposomes to interact with EG.
The lipid mixing between SA-liposomes and platelets was not affected b
y CM-chitin or phagocytosis inhibitors: EDTA, cytochalasin B, or 2,4-d
initrophenol and iodoacetate, indicating the importance of glycoprotei
ns on the platelet membrane surface in the interaction of SA-liposomes
with platelets.