before the radium was fixed in tissue.
Without data to support another conclu-
sion, Hamilton probably assumed that
the behavior of plutonium would be
similar—much of it would be eliminat-
ed quickly.
Hamilton also suggested that “integra-
tion of 24-hour urine samples, checked
every 2 weeks will give a fairly good
indication of intake of Pu by an indi-
vidual, and so a gauge of Pu deposition
in body.” This statement is consistent
with the assumption that, like radium,
plutonium would take time to become
fixed in tissue. Thus, an accurate deter-
mination of a body burden would re-
quire that the measurements be made
after the plutonium circulating in the
blood was either excreted or fixed. At
that later time, only plutonium re-enter-
ing the blood from fixed tissue sites
would be circulating, and measurements
of the fraction excreted would more ac-
curately reflect the level of retained
plutonium.
Eleven milligrams of plutonium were
diverted to Hamilton at the beginning
of February 1944 (about 2 per cent of
the total Clinton output of plutonium at
that point) to enable him to begin bio-
medical experiments with animals. The
research involved administering soluble
15-microgram portions of plutonium-
239 compounds to rats, using different
plutonium valence states (+3, +4, and
+6) and different methods of introduc-
ing the plutonium (oral, intramuscular,
intravenous, subcutaneous, and intrapul-
monary procedures).
A Met Lab progress report for February
containing Hamilton’s input stated:
Product studies: - Oral absorption
of all valence states is less than
0.05%; lung retention high; ad-
sorbed material predominately in
skeleton; excretion very small in
urine and feces.
And the report for March noted:
Product behaves differently in the
three valence states. The plus 4
state is retained to considerable ex-
tent at 16 days, the plus 3 is re-
tained to a less degree and the plus
6 to a still less degree.
By April, Hempelmann was discussing
Hamilton’s results at Los Alamos, say-
ing that “plutonium in all three valence
states is very poorly absorbed when
taken by mouth—less than .005%” and
“the organ which took up most of the
absorbed plutonium was the bone, with
more than half of the element going to
the skeletal system in each case.”
Additional quantities of plutonium were
made available to Hamilton, and he was
authorized to extend his research to the
uptake of plutonium dust from the
lungs of rats. He soon learned that
only about 20 per cent of the plutonium
originally inhaled was eventually de-
posited in the skeleton. Almost half
was trapped in the upper air passages
and eliminated; about 25 per cent re-
mained in the lung, although some of
that was slowly eliminated. The actual
percentages depended on whether or
not the plutonium compound was solu-
ble—plutonium nitrate was quite readi-
ly absorbed, whereas the oxide was not
absorbed at all.
In the spring of 1944, plutonium was
made available for animal studies at the
Chicago Met Lab, and research was ini-
tiated there on the acute toxicity of plu-
tonium. Those studies involved the in-
jection of microgram and milligram
quantities of plutonium-239 into mice,
rats, rabbits,.and dogs.
The results of the studies at Berkeley
and Chicago showed that plutonium’s
physiological behavior differed signifi-
cantly from that of radium. Two facts
were particularly alarming: there was
significant deposition of plutonium in
the liver, and the overall excretion rates
were very low (see Table 1). Neither
of these facts were anticipated when the
tentative 5-microgram tolerance limit
for plutonium was adopted early in
1944. Furthermore, the rate of plutoni-
um elimination in excreta differed be-
tween species of animals by as much as
a factor of five. Such variation made it
difficult to estimate what the rate would
be for man.
The studies also showed that plutonium
was similar to radium in being a bone
seeker, but only a little more than half
of what was retained went to the bone,
compared to 99 per cent for radium.
Also, the two metals deposited at dif-
ferent locations. Radium (similar,
chemically, to calcium) deposited in
mineralized bone, whereas plutonium
remained on the surface in the “actively
metabolizing” portion of the bone, an
area intimately associated with bone
marrow and the production of blood
cells. (However, because plutonium
deposits on the endosteal surfaces of
the red marrow and the alpha particles
have a limited range, the blood-forming
tissue is not irradiated uniformly.)
The initial animal excretion rate for
plutonium was low (less than 10 per
cent of what had been introduced ap-
peared in the urine and about 6 per cent
in the feces over the first four days),
The Human Plutonium Injection Experiments
188
Los Alamos Science Number 23 1995
Joseph Hamilton carried out the ini-
tial metabolic studies of plutonium in
animals.