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Vasc Med ; 15(4): 307-13, 2010 Aug.
Article in English | MEDLINE | ID: mdl-20724376

ABSTRACT

Liposomes have been used as imaging and therapeutic agents in various tissues but only infrequently in the cardiovascular system. We prepared a liposome to target atheromas in a Watanabe heritable hyperlipidemic (WHHL) rabbit model. Liposomes labeled with rhodamine and nanogold were injected intra-arterially into the descending thoracic aortas of WHHL rabbits. The arterial segments of interest were perfusion-fixed and evaluated with immunohistochemistry, light microscopy, and electron microscopy. Deconvolution microscopy showed that rhodamine label was concentrated in the plaque shoulder regions of advanced-stage atheromas; however, rhodamine label was not found in adjacent, non-atherosclerotic aorta. Transmission electron microscopy revealed liposome remnants and the highest concentration of nanogold label in lipid-laden areas of atheromas. Liposomes were concentrated in areas of lipoprotein-associated phospholipase A(2) expression. We conclude that modified liposomes can be delivered to the shoulder regions of advanced atheromas in WHHL rabbits and may be useful therapeutically for targeting metabolically active plaque.


Subject(s)
Drug Delivery Systems/methods , Hyperlipidemias/drug therapy , Liposomes/pharmacokinetics , Plaque, Atherosclerotic/drug therapy , 1-Alkyl-2-acetylglycerophosphocholine Esterase/metabolism , Animals , Aorta, Thoracic/metabolism , Aorta, Thoracic/ultrastructure , Disease Models, Animal , Freeze Fracturing , Gold/pharmacokinetics , Hyperlipidemias/genetics , Injections, Intra-Arterial , Liposomes/chemistry , Metal Nanoparticles , Microscopy, Electron , Plaque, Atherosclerotic/genetics , Rabbits , Rhodamines/pharmacokinetics
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