Self-assembling nanoparticles functionalized with targeting moieties have
significant potential for atherosclerosis nanomedicine. While self-assembly
allows for easy construction (and degradation) of nanoparticles with therapeutic
or diagnostic functionality, or both, the targeting agent can direct them to a
specific molecular marker within a given stage of the disease. Therefore,
supramolecular nanoparticles have been investigated in the last decade as
molecular imaging agents or explored as nanocarriers that can decrease the
systemic toxicity of drugs by producing accumulation predominantly in specific
tissues of interest. In this review, we first describe the pathogenesis of
atherosclerosis and the damage caused to vascular tissue, as well as the current
diagnostic and treatment options. Then we provide an overview of targeted
strategies using self-assembling nanoparticles and include liposomes, high
density lipoproteins, protein cages, micelles, proticles, and perfluorocarbon
nanoparticles. Finally, we elaborate on and provide an overview of current
challenges, limitations, and future applications for personalized medicine in
the context of atherosclerosis of self-assembling nanoparticles.