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Nanotechnology Enables Low-Dose Treatment
of Atherosclerotic Plaques
In laboratory tests, one very low dose of a drug was
enough to show an effect on notoriously tenacious artery-clogging
plaques. What kind of drug is that potent?
It's not so much the drug itself as how it was delivered.
Fumagillin -- a drug that can inhibit the growth of
new blood vessels that feed atherosclerotic plaques
-- was sent directly to the base of plaques by microscopically
small spheres called nanoparticles developed by researchers
at Washington University School of Medicine in St. Louis.
"Previously we reported that we can visualize plaques
using our nanoparticle technology, but this is the first
time we've demonstrated that the nanoparticles can also
deliver a drug to a disease site in a living organism,"
says Patrick Winter, Ph.D., research assistant professor
of medicine. "After a single dose in laboratory
rabbits, fumagillin nanoparticles markedly reduced the
growth of new blood vessels that feed plaques."
An atherosclerosis plaque results when a buildup of
cholesterol, inflammatory cells and fibrous tissue forms
inside an artery. If a plaque ruptures, it can block
blood flow to the heart or brain, causing heart attack
or stroke.
While growing, plaques require an influx of nutrients,
fats and cells, so they develop their own blood supply
-- minute blood vessels that grow within the wall of
arteries and penetrate the plaque. Many believe that
cutting off this blood supply could stabilize or reduce
plaques. In previous studies, fumagillin has been shown
to be an effective agent for stopping the process that
creates new blood vessels.
Riding on the nanoparticles, fumagillin is carried to
the site of new blood vessel formation and stays there
thanks to a fellow nanoparticle passenger -- a component
that fastens the nanoparticles to cells found in newly
developing blood vessels. Stuck in this position, the
nanoparticle drops its load of fumagillin, concentrating
it at the site of the atherosclerotic plaque.
In this study, the single dosage of fumagillin each
rabbit received was 50,000 times lower than the total
fumagillin dose used in an earlier experiment by another
research group and yet reduced the growth of new blood
vessels in plaques by 60 to 80 percent.
"Fumagillin can have neurocognitive side effects,
causing injury to the brain at high doses," Winter
says. "The ability of the nanoparticles to concentrate
the drug at the disease site allows the dose to be lowered.
This could open the door for a lot of drugs that have
failed to be approved because they caused too many side
effects at a higher dose. It might pay to look at these
drugs again and ask if placing them on these nanoparticles
can help them be effective at a lower dose and clinically
useful."
The nanoparticles are the invention of Samuel Wickline,
M.D., professor of medicine, of biomedical engineering,
of physics and of cell biology and physiology, and Gregory
Lanza, M.D., Ph.D., associate professor of medicine
and biomedical engineering. Both are heart specialists
at Barnes-Jewish Hospital.

These before (left) and after images
show the effects of fumagillin-laden nanoparticles,
which inhibit the growth of plaque-feeding microvessels,
in a rabbit aorta.
The microscopic spheres are capable of carrying a variety
of components at the same time and can be detected with
standard MRI scans, making them useful for imaging disease
sites while simultaneously treating them. Using the
nanoparticles, a physician can confirm a drug has reached
the desired location, measure the amount of drug at
the site, and later check to see if the drug has affected
the disease.
In the current study, the researchers fed rabbits a
high-cholesterol diet for 80 days before treatment with
fumagillin nanoparticles. The diet caused numerous small
plaques in the rabbits' aortas, but the plaques were
considered to be at an early stage of growth. By demonstrating
the utility of the nanoparticles for early intervention
of atherosclerosis, the research group hopes that they
can help alleviate the need for more invasive treatment
of later-stage atherosclerosis.
"We wanted to go after the early stages of the
disease when patients don't yet need immediate intervention
to prevent serious cardiac problems," Winter says.
"We think fumagillin nanoparticles potentially
could be incorporated into a protocol that includes
lipid-lowering statin drugs or dietary changes."
Next, the research group plans to study the effect of
fumagillin nanoparticles in the treatment of cancerous
tumors. According to Winter, the use of inhibitors of
blood vessel growth is a well-accepted therapy for cancer,
suggesting the nanotechnology may prove beneficial in
cancer therapy.
Visit http://medschool.wustl.edu

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