P. Borel et al., CAROTENOIDS IN BIOLOGICAL EMULSIONS - SOLUBILITY, SURFACE-TO-CORE DISTRIBUTION, AND RELEASE FROM LIPID DROPLETS, Journal of lipid research, 37(2), 1996, pp. 250-261
Data on the physico-chemical properties of carotenoids in biological e
mulsions are essential to our knowledge of carotenoid metabolism. Ther
efore, we determined the behavior of carotenoids in phospholipid-stabi
lized triglyceride emulsions, a model for biological emulsions such as
dietary emulsions, triglyccride-rich lipoproteins, and intracellular
storage droplets. The solubility of beta-carotene (a model for apolar
carotenoids, carotenes) in pure bulk triglycerides (0.112 to 0.141 wt
% according to triglycerides) was significantly higher than zeaxanthin
(a model for polar carotenoids, xanthophylls) (0.022 to 0.088 wt %).
The solubility of both carotenoids increased when the chain-length of
the triglycerides' fatty acids decreased. The amount of zeaxanthin ass
ociated with lipid droplet dramatically increased in phospholipid-trig
lyceride droplets as compared to the pure corresponding triglyceride d
roplets, whereas the amount of beta-calotene associated with lipid dro
plets increased only slightly. beta-carotene distributed almost exclus
ively in the core of triolein-lecithin-carotenoid droplets, while zeax
anthin distributed preferentially at the droplet's surface. A signific
ant percentage (8.3%) of zeaxanthin was spontaneously transferred from
lipid droplets to aqueous phase and the remaining part was transferre
d during triglyceride hydrolysis catalysed by pancreatic lipase, while
beta-carotene absolutely required triglyceride lipolysis to be transf
erred to the aque-ous phase. Our results show that polar and apolar ca
rotenoids behave differently in biological emulsions. They further our
understanding of the bioavailability of polar and apolar carotenoids
and of their distribution between lipoprotein particles.