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question on PET radioisotope production in reactors
Dear Radsafers,
Perhaps one or two of you can help me answer this question, please.
A friend provided the following reference recently (see below), about the
production of the popular PET radioisotope fluorine-18 using a two-step
nuclear reaction which starts with an (n,alpha) reaction, in a fission
reactor (as opposed to the standard method of production using >20 MeV
protons from a cyclotron, by way of 18O(p, n)18F ).
I would be interested in a comparison of the reaction rates in the two
production methods, as well as information on whether nuclear medicine labs
equipped with small reactors have used them for PET radioisotope production
(and if not, why not ?).
The reason I'm asking is that it seems to me that if one can get both PET
and neutron-activated radioisotopes from one source - a reactor (at those
labs that have one) - then the cyclotron would appear to be superfluous.
Thank you very much, in advance.
Jaro
http://www.cns-snc.ca/branches/quebec/quebec.html
-----Original Message-----
Sent: Friday December 19, 2003 11:06 AM
To: 'Franta, Jaroslav'
Subject: RE: cyclotrons vs reactors ?
FYI, I found a PET isotope prescription (F18) in an old reference.
In the document by W.E. Downs and D.J.R. Evans entitled "Slowpoke - A
mini-reactor for activation analysis", AECL Commercial Products, Research
Division, CPSR-327 (June 1971) [to bepresented at the 2nd symposium on
recent developments in neutron activation anslysis - Churchill College,
Cambridge, Jue 28, 1971 to July 1, 1971], we find the following double
nuclear reaction (p. 12):
Li6(n,alpha)t
O16(t,n)F18
"Irradtaion of a saturated solution of 6Li2+ in acetic acid (5 ml) allows
for the preparation of up to 20 mCi of F18 in a single irradiation. The
separation protocol proposed by Dworkin and Lafleur may be applied to the
irradiated solution."
Ref: H.J. Dworkin, P.D. Lafleur, "Radioactive Pharmaceuticals", p. 635,
USAEC CONF 651111, 1966.
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