Liposomes can be used as model systems to study the oxidation of phospholip
ids of meat products, providing an understanding of their characteristics a
nd stability. Liposomes made of muscle phospholipids were prepared using th
ree methods. They exist in multilamellar vesicles, small unilamellar vesicl
es and large unilamellar vesicles, as seen by electron microscopy of freeze
-fractured samples. Fatty acid and class compositions of liposomes and phos
pholipid extracts were Similar. In small unilamellar vesicles and large uni
lamellar vesicles, conjugated dienes and thiobarbituric acid values (TBA-rs
) were slightly higher than in multilamellar vesicles and phospholipid extr
acts, but they remained at a very low level. During storage at 4 degrees C
in air, polyunsaturated fatty acids, the phosphatidyl ethanolamine/phosphat
idyl choline ratio, conjugated dienes and TBA-rs were stable for at least 7
d Turbidity of small unilamellar vesicles and large unilamellar vesicles i
ncreased slightly with time, indicating changes in the size distribution of
liposomes. Liposomes can therefore be prepared from muscle phospholipids w
ith no major deterioration in lipids. Furthermore, their stability during s
hort term storage (3, d) is good. The method chosen to prepare liposomes sh
ould take into account the physical structure of liposomes, which can inter
fere with further experiments. (C) 1999 Academic Press.