A new device, the chemical equivalent of a
transistor, might make possible ultrasensitive bio-medical
single-antigen detection.
The things we associate with transistors,
the closing or opening of a switch or the amplification of a signal,
are normally carried out by injecting a tiny electric signal into a
gate electrode which then changes the environment of a nearby
channel region. This allows a current to be shut off or to be
amplified. In an experiment carried out by physicists at the
University of California at Irvine, the same things are done through
chemical reactions.
Philip Collins (collinsp@uci.edu,
949-824-9961) and his colleagues use carbon nanotubes as the central
working substance of their device. The nanotubes, immersed in a
liquid, can be switched from a conducting state to an insulating
state by oxidizing them -- that is, by chemically removing the free
electrons. The chemical reactions are triggered by an electrical
potential applied across the interaction area (figure at
Physics News Graphics).
What the Irvine researchers
show is that this
process can be performed reversibly and over short periods of time,
as fast as 10 microseconds. This is quite slow by today's
transistor standards; the more important promise for prospective
chemical field effect transistors (or ChemFETs) is the potentially
large amplifications. It looks as if only a few electrons' worth of
oxidation can be used to switch currents as large as microamps.
In a future bio-detector the switching would be provided not by an
applied electrochemical signal but by the trace presence of antigens
docking with antibodies attached to the nanotubes. In previous
detectors, chemical actuation has required the presence of tens of
antigens; here, a single antigen might be enough to change the state
of the nanotube.
Mannik et al.,
Physical Review Letters, 7 July 2006
Contact Philip Collins, University of California at Irvine
collinsp@uci.edu
Tel: 949-824-9961
Image at
Physics News Graphics
Philip Collins' Research Group