NRI
developed Biodegradable Polymers May Improve Treatment of Inflammatory
Diseases
in acute lung
injury, acute liver failure and inflammatory bowel disease
Atlanta, Georgia, Aug 21, 2008
Abby Vogel, Georgia Tech
Polyketal microparticles show promise as drug delivery vehicle
A family of biodegradable polymers called polyketals and their
derivatives may improve treatment for such inflammatory illnesses
as acute lung injury, acute liver failure and inflammatory bowel
disease by delivering drugs, proteins and snips of ribonucleic acid
to disease locations in the body.
“The polyketal microparticles we developed are simply a vehicle
to get the drugs inside the body to the diseased area as quickly
as possible,” said Niren Murthy, assistant professor in the
Coulter Department of Biomedical Engineering at Georgia Tech and
Emory University. “The major advantage to using these polyketals
to deliver drugs is that they degrade into biocompatible compounds
that don’t accumulate in a patient’s tissue or cause
additional inflammation.”
Details about the polyketals and clinical applications were described
during three presentations on August 18-20 at the 236th American
Chemical Society National Meeting in Philadelphia. This research
– initially started in 2003 – is funded by the National
Science Foundation and the National Institutes of Health.
In a presentation on August 19, graduate student Scott Wilson detailed
a new polyketal derivative aimed at enhancing the treatment of inflammatory
bowel disease – an illness that causes the large and small
intestines to swell.
The new polymer has the advantage of stability in both acids and
bases. It degrades only in the presence of reactive oxygen species,
which are present in and around inflamed tissue. Cell culture experiments
have demonstrated that the microparticles degraded more rapidly
in cells that overproduced superoxide, a reactive oxygen species
The researchers are currently collaborating with Didier Merlin,
a professor in the Division of Digestive Diseases at Emory University,
to investigate loading these polyketals with therapeutics to treat
inflammatory bowel disease.
“We think these microparticles are going to be fantastic
for oral drug delivery because they can survive the stomach conditions
before they release their contents in the intestines,” noted
Murthy.
Murthy’s group is also examining the use of polyketals to
treat acute liver failure – a condition in which the liver
stops functioning because macrophages in the liver create reactive
oxygen species. One treatment is the delivery of superoxide dismutase,
an enzyme that detoxifies superoxide. Incorporating the enzyme inside
a polyketal – poly(cyclohexane-1,4-diyl acetone dimethylene
ketal) – allows the enzyme to be released very quickly in
an acidic environment.
“Patients with acute liver failure need drugs as soon as
possible or else they’ll die,” said Murthy. “We’ve
tailored the polyketal’s hydrolysis rates to deliver the drug
in one or two days.”
Nick Crisp, professor of microbiology and immunology at the University
of Rochester Medical Center, and Robert Pierce, currently head of
anatomic pathology at Schering-Plough Biopharma and formerly of
the University of Rochester Medical Center, are collaborating on
this project. Georgia Tech, Emory and the University of Rochester
have filed three patent applications on the polyketal drug delivery
system.
Polyketal microparticles – used as a vehicle to deliver therapeutics
to an affected region of the body – degrade into biocompatible
compounds that don’t accumulate in a patient’s tissue
or cause additional inflammation. (Georgia Tech Photo: Gary Meek)
300 dpi Hi-Res Version
To treat other illnesses, it may be necessary to deliver proteins
to a diseased organ. In a presentation on August 18, Georgia Tech
researchers described such a method, which was developed by Murthy,
Michael Davis, an assistant professor in the Coulter Department
of Biomedical Engineering, and graduate student Jay Sy.
“Delivering proteins inside microparticles has been limited
because getting the protein into the microparticles required organic
solvents that frequently destroyed the proteins,” explained
Murthy. “To overcome this problem, we developed a method of
simply immobilizing the protein on the surface of the microparticles.”
The researchers incorporated a nitrilotriacetic acid-lipid conjugate
into the polyketal. In a one-step procedure, they mixed the microparticles
with the proteins and centrifuged them. That immobilized the proteins
on the surface of the polyketals. Laboratory experiments conducted
under physiological conditions have shown that half of the bound
proteins were released within 24 hours.
Also in collaboration with Davis, the researchers are testing the
ability of the protein-bound polyketals to treat heart attacks.
In the next few years, Murthy and his team of graduate students
and collaborators plan to continue developing new polyketals and
conducting efficacy tests in cell cultures and animal studies.
“In the past few years, we have developed methods to tailor
the polyketal’s properties, which have already allowed us
to target many different medical conditions, but our end goal is
to test these treatments in humans,” noted Murthy.
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