New reactor needed for medical imaging
- why cyclotrons cannot do the job
Article
from Australasian Science Magazine
Rex
Boyd defends the decision to commission a new nuclear reactor.
It
is claimed by opponents of the nuclear industry that Australia's
demand for medical radioisotopes can be met by cyclotrons.
The truth is that any number of cyclotrons will never replace
Australia's need for a reactor.
Australia
has two cyclotrons, which use high voltages and electrical
fields to accelerate hydrogen atoms through a vacuum chamber.
When they collide with a target substance they produce radioactivity.
As
a general rule, it is more difficult to make a radioisotope
in a cyclotron than in a reactor. Cyclotron reactions are
less productive and less predictable than nuclear reactions
performed in a reactor.
The
cyclotron produces neutron-deficient radioisotopes whereas
the reactor produces neutron-rich radioisotopes. Thus the
reactor and the cyclotron complement each other in satisfying
society's need for a full range of radioisotopes; rarely
one acts as a substitute for the other.
A few
radioisotopes are exceptions to this rule and can be produced
by either facility. One is technetium-99m, currently used
in 85% of medical applications. The discovery that technetium-99m
can be produced in a cyclotron does not imply that the need
for a reactor is disappearing.
The
half-life of technetium-99m is 6 hours. This means that
this radioisotope must be produced and distributed on a
daily basis.
However,
when technetium-99m is produced in a reactor it proceeds
through a precursor radioisotope, molybdenum-99, which has
a half-life of 66 hours. Thus the weekly production of molybdenum-99
generators can meet all the technetium-99m needs of Australian
hospitals.
In
contrast the cyclotron does not produce molybdenum-99; instead
it produces technetium-99m directly. Therefore a network
of cyclotrons situated across Australia would be needed
to make daily deliveries of technetium-99m to the nation's
hospitals. This is one reason why none of the many powerful
cyclotrons around the world are used for the manufacture
of technetium-99m.
Reliance
on cyclotrons for our most frequently used medical isotope
would have a serious negative impact on the practice of
nuclear medicine. The rapid decay of technetium-99m would
limit the number of patients treated in any one day and
would preclude the use of nuclear medicine techniques in
out-of-hours emergency situations when stocks would be exhausted.
Appointments would be subject to technetium-99m availability
and patient waiting lists would lengthen.
Economic
factors would also militate against cyclotron-produced technetium-99m.
The raw materials for reactor production are cheap (a few
dollars per kilogram) and readily available, whereas the
starting material for the cyclotron-method is a rare form
of molybdenum that must be enriched to high levels of isotopic
purity (>99%), is not commercially available and would cost
millions of dollars per kilogram.
Traces
of other molybdenum isotopes in the raw materials can reduce
the purity of the technetium-99m. A series of competing
nuclear reactions produces undesirable longer-lived technetium
radioisotopes, particularly technetium-96, that can accumulate
during theday. The level of these impurities may exceed
the legal limit and degrade the quality of the scanned image.
Other
technetium radioisotopes would expose patients to higher
radiation doses. Only 0.1% technetium-96 is necessary before
radiation exposure of patients is doubled. Hence before
cyclotron-produced technetium-99m could be used, certain
regulations governing radiopharmaceutical quality would
need changing.
The
cyclotron production of technetium-99m is technically feasible
but undesirable for all of these reasons.
The
frontiers of nuclear medicine now extend beyond the diagnosis
of disease with technetium-99m. Other short-lived radioisotopes
are being introduced into nuclear medicine with the capability
of reducing the pain associated with cancer. Australia must
have its own reactor if its community is to have access
to these radioisotopes and reap the benefits of the latest
advances.
Rex
Boyd was formerly the director of the $20 million National
Medical Cyclotron Project at Sydney's Royal Prince Alfred
Hospital.
Main
sources for biefing paper:
ANSTO, and papers at 1999 and 2001 ANA conferences.
NRPB Bulletin #231, Sept 2001.
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