he duplicated. There is considerably less variety in

sments of

1. Oral Biol. choice of materials employed. While rice, sugar, or
F .imilar granular materials are frequently used to simu-

Inte the uncontaminated body, it is the almost uni-

versal custom to employ aqueous solutions whenradioiJ. Microseogk .«livity is to be incorporated therein. I’or intensive and
'adiat. Res.
ried use, a phantom containing radioactive liquid
F ..- several practical disadvantages, namely the everF present danger of leakage, which maylead to contamim of Calei F uation of expensively shielded detectors and enclosure,
153 (1963),
and the inconvenience of cross contamination between
ill, J. H. Co
- different isotopes used within the phantom itself. The
of Cats

Iutter counsels the use of short-lived materials, and the
n Annual RE additional labor that their use entails. These problems
189, pp. 24-38 increase in importance with the complexity in detail
tion of the Ig i the phantom.
Biologicalk
Less hazardous and tedious manipulation may be
ratory Radié
abtained by incorporating the desired radioelement
ort, Januan
ynne Nation

into beads of suitable size. These may be poured from

y, J. Radiuk ~tornge container to phantom manytimes with quan-

’ titative transfer. While they are still subject to accidental spillage, recovery and salvage are considerably
m in Hume,
simplified. We have recently investigated the pracBone. Radio,
tirnlity of such a system, and present here a progress
w-Hill, Nei report on some of its advantages and problems.
Appearan

|

A.J., Schol,
itive Micry
seratic Bone

PREPARATION OF BEADS

‘:.dioactive microspheres of either ceramic or plastic

material are available from the 3M Companyin sizes
ringing
from 10 to 150 micrometers.“ On special
4J., Arnstein®
.
é
ycline-B ase, order, they supplied us with much larger plastic spheres,
te and Cel 725 + 70 in diameter. Specific activities normally
Orthoped. 46° produced range from 0.1 to 30 Ci/g. These activity levels
-re not compatible with our intended use, but, again
the Alkaline
bs special request, we obtained spheres loaded with
resium-137
and eobalt-60 at approximately 1.3 wCi/g.
Institute o
The
spheres
are much too small to handle individS10,
uly or to locate if accidentally spilled (about 5000/g);
therefore, we obtained nylon beads 5.5mm diameter
» with a I-mm hole drilled to the approximate center of
Fenech. (The indentation will hold about 20 microspheres,) A fixed number of spheres were placed in
cach eavity and sealed in place with a drop of low\isvosity epoxy cement. A vacuum pickup device,
udjusted to accept a fixed number of spheres, devised
by Mr, E. Fudala of the Radiological Physics Division
stuff shop, greatly simplified the loading procedure.
) simulate

STANDARDIZATION

Whenliquid sources are used, a uniform distribution
automatically results. With discrete beads, one must

either (1) assay each bead separately, identify it
uniquely, and sum the total activity in a given source,

or (2) determine the mean activity level of the beads

and their distribution about that value. We chose the
latter course for obvious reasons.
One hundred microspheres were counted repetitively
(a different sample each time) with a total of 58 samples;
a few additional runs were made with only 10 or 20
microspheres, i.e., single beads. Table 31 summarizes
the results.

Data are expressed as net counts per minute in the

entire photopeak, as detected by a 17.8-cm diameter

by 8.9-cm thick Nal crystal and single channel ana-

lyzer. Sources were placed in accurately reproducible
geometryon the crystal face.
The first loading of beads was carried out using

microspheres from the top of the container. The abso-

lute activity level was about 30% greater than that
inferred from the assay supplied by the 3M Company.
Wespeculated that perhaps the discrepancy might be
due to nonuniform labeling of the plastic resin spheres,

which were then insufficiently intermixed and ran-

domized during subsequent processing and shipping.
Hence we sampled spheres taken from the midplane
and bottom of the container and noted significant
differences, though nothing like 30% (see lines 4 and 5
Table 31). The large values of chi squared indicated

that the samples tested do not represent a normal

distribution. We observe that many spheres are in
actuality more like half-spheres, with a smaller fraction
of intermediate shapes. It has been suggested that
allowing the spheres to roll down a shghtly inclined
plane would separate those with large flat surfaces and
hence improvethe uniformity, and we intend to trythis.
With this activity level, filling a liver or kidneyentirely with source beads results in an inconveniently
large total activity. The remedyis to use the required
number of active beads, diluted with additional nonradioactive ones. For economy, the latter may be of
Lucite instead of nylon. As a practical matter, we think

it likely that not more than 100 active spheres will

usually suffice for a given requirement. The number

actually used maywell be determined bythestatistical
distribution in space required to simulate a uniform

e purporf Migure 57 illustrates beads held in a simple polyethylene

distribution, rather than by the precision in total

f varying, Cich lot was
sprayed with paint of a distinctive color to
e physica,
“‘cird against accidental admixture and to facilitate
dy are té
' !rleval if inadvertently dropped.

0.7 g/cm. For accurate stmulation of the larger organs,
where self-absorption may be appreciable, fine granules
could be added to increase the density to unity.

ion equip? jig while being loaded and sealed. Beads were loaded
With each isotope at two specific activity levels, and

activity.

The mean density of close-packed beads is about

Select target paragraph3