| CHAMPAIGN,
Ill. - Protein-encapsulated single-walled carbon nanotubes
that alter their fluorescence in the presence of specific
biomolecules could generate many new types of implantable
biological sensors, say researchers from the University
of Illinois at Urbana-Champaign who developed the encapsulation
technique.
In a paper accepted for publication
in the journal Nature Materials, and posted on its
Web site, the researchers showed the viability of
their technique by creating a near-infrared nanoscale
sensor that detects glucose. The sensor could be inserted
into tissue, excited with a laser pointer, and provide
real-time, continuous monitoring of blood glucose
level.
"Carbon nanotubes naturally
fluoresce in the near-infrared region of the spectrum
where human tissue and biological fluids are particularly
transparent," said Michael Strano, a professor
of chemical and biomolecular engineering at Illinois.
"We have developed molecular sheaths around the
nanotube that respond to a particular chemical and
modulate the nanotube's optical properties."
To make their biological sensors,
Strano, postdoctoral research associate Seunghyun
Baik, and graduate students Paul Barone and Daniel
Heller begin by assembling a monolayer of the enzyme
glucose oxidase on the surface of nanotubes suspended
in water. The enzyme not only prevents the nanotubes
from sticking together into useless clumps, it also
acts as a selective site where glucose will bind and
generate hydrogen peroxide.
Next, the researchers functionalize
the surface with ferricyanide, an ion that is sensitive
to hydrogen peroxide. The ion attaches to the surface
through the porous monolayer. When present, hydrogen
peroxide will form a complex with the ion, which changes
the electron density of the nanotube and consequently
its optical properties.
"When glucose encounters
the enzyme, hydrogen peroxide is produced, which quickly
reacts with the ferricyanide to modulate the electronic
structure and optical characteristics of the nanotube,"
Strano said.
"The more glucose that is present, the brighter
the nanotube will fluoresce."
To prove the practicality of
their technique, Strano's team loaded some of the
sensors into a porous capillary that confined the
nanotubes but allowed glucose to enter. When inserted
into human tissue, the fluorescent emission of the
sensor corresponded to the local glucose concentration.
"The advantage of the
near-infrared signaling to and from such a capillary
device is its potential for implantation into thick
tissue or whole blood media, where the signal may
penetrate up to several centimeters," Strano
said. "And, because nanotubes won't degrade like
organic molecules that fluoresce, these nanoparticle
optical sensors would be suitable for long-term monitoring
applications."
One important aspect of the
new surface chemistry, Strano said, is that no bonds
are broken on the nanotube. "This allows us to
shuttle electrons in and out without damaging the
nanotube itself."
Another important aspect is
that the technique can be extended to many other chemical
systems. "We've shown that it is possible to
tailor the surface to make it selective to a particular
analyte,"
Strano said. "There are whole classes of analytes
that can be detected in this manner."
The National Science Foundation
funded the work. The researchers have applied for
a patent.
CONTACT: James E. Kloeppel,
Physical Sciences Editor 217 244-1073; <mailto:kloeppel@uiuc.edu>.
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