N. Savion et al., ROLE OF BLOOD COMPONENTS IN OCULAR SILICONE OIL EMULSIFICATION - STUDIES ON AN IN-VITRO MODEL, Investigative ophthalmology & visual science, 37(13), 1996, pp. 2694-2699
Purpose. To develop an in vitro model for silicone oil emulsification
and to explore the blood components involved in this process. Methods,
The capacity of various blood components to support silicone oil (100
0 CS) emulsification was studied by applying 0.5 mi oil on top of 0.5
mi saline containing various blood components. Each tube was sonicated
for 150 seconds and centrifuged at 5000g for 20 minutes. Three phases
were noted in the tube: At the top was clear silicone oil, in the mid
dle was emulsified silicone oil, and at the bottom was aqueous solutio
n. The tubes were photographed, and the percentage of the phase length
containing emulsified silicone oil (middle) of the total length of th
e three phases was calculated from the projected image of each tube. R
esults, Emulsified silicone oil in plasma or serum was initiated after
100 seconds of sonication and quickly reached maximum (approximately
80%) at 120 seconds. The size of these oil droplets prepared in vitro
was 0.0467 +/- 0.028 mm, closely resembling that observed in oil sampl
es removed from a patient's anterior chamber (0.038 +/- 0.018 mm). Und
er these conditions, silicone oil emulsified in the presence of whole
blood cells occurred only at a concentration of 120 mu g protein/ml; i
n the presence of red blood cell membranes, it occurred at a concentra
tion of 60 mu g protein/ml. Lipoprotein-deficient serum failed to supp
ort emulsification; however, samples of high-density lipoprotein and l
ow-density lipoprotein supported this process. Purified high-density l
ipoprotein-apolipoproteins supported oil emulsification. The addition
of phosphatidylcholine further enhanced this process, but phosphatidyl
choline alone failed to support emulsification. Conclusions. A simple
and fast in vitro model to study factors affecting silicone oil emulsi
fication was developed. Using this model, red blood cell membranes, pl
asma lipoproteins, and purified HDL-apolipoproteins supported silicone
oil emulsification. Lipids did not, but they had the capacity to enha
nce the apolipoprotein-supported emulsification.