Putting
pharmaceutical agents into the body isn't hard, but
getting them into targeted areas can be problematic.
If drugs aren't taken up by a large enough proportion
of cells, a suitable “transport agent” must be used.
A French and Italian research team has successfully
used carbon nanotubes as transport agents for antimycotics
(antifungal agents). In addition, they have developed
a strategy for attaching a second agent or marker
to the nanotubes in a controlled fashion.
Carbon nanotubes are long, narrow nanoscale tubes
made of multiple layers of carbon atoms arranged
in graphite-like sheets. “They can drill through
cell membranes like tiny needles,” explains Alberto
Bianco, “without damaging the cell.” If proteins
or nucleic acids are attached to the nanotubes, they
come right along through the membrane. Bianco and
a team of scientists from CNRS (Centre National de
la Recherche Scientifique of Strasbourg and the University
of Trieste wanted to determine if this concept could
also be extended to small pharmaceutical molecules
such as antibiotics or cancer drugs. They were particularly
intrigued by the idea of attaching not one, but two
different “passengers”. This would make it possible
to carry out combination therapies with two different
drugs or to trace the uptake of a drug by using a
marker.
Attaching two different molecules to a carbon nanotube
in a targeted, controlled, and fully independent
manner requires a clever strategy. The researchers
thus put two different types of anchor sites, equipped
with protective “caps”, on the tips and sides walls
of the tubes. They removed the first type of “cap” and
attached one kind of molecule, then removed the second
type of cap and attached another type of molecule.
The researchers thus loaded the nanotubes with the
antimycotic amphotericin B, as well as a fluorescence
dye.
When coupled to the nanotubes, the drug loses the
toxic side effects typical of treatment with amphotericin
B. At the same time, its effectiveness against fungi
is improved. One reason for this could be the improved
solubility in water; in addition, the amphotericin
is prevented from forming clumps. “Our approach could
help amphotericin B become more widely used against
chronic fungal infections,” hopes Bianco.
A particularly attractive target is carbon nanotubes
equipped with both a drug and a “guide”. The guide
could then recognize certain types of cells, such
as tumor cells, and could conduct the transporter
to these cells to deliver the drug preferentially
to where it is needed.
Author: Alberto Bianco, Institut de Biologie Moléculaire
et Cellulaire, Strasbourg (France), http://www-ibmc.u-strasbg.fr/Pages_perso/english/a_bianco.html
Title: Targeted Delivery of Amphotericin B to Cells
by Using Functionalized Carbon Nanotubes
Angewandte Chemie International Edition ,
doi: 10.1002/anie.200501613
Contact : Editorial office: angewandte@wiley-vch.de or
David Greenberg (US): dgreenbe@wiley.com or
Julia Lampam (UK): jlampam@wiley.co.uk
Angewandte Chemie , Postfach 101161, 69495
Weinheim, Germany.
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