SDR abe ea ale anil a alatidcts fhnthe

106
TABLE 45.
Batch No. | Ant | Code || Dura- ||

|

L2878

|

!

\

Man |

O02

!
Man;

08

Sample

|

40d

|

|
; 49d

Ra 22Th
—

' Rat !
Man:
| Man:

[Rat

Rat
i Rat
| Rat

72
8&3
85

0.51:

' Vertebra®
Rib™
Vertebra™

0.430:
0.38
1.2

| Long bones
| Femur
| Skull

6.1
1.7
—

TH2 | 18m | Long bones)

Man

66

—
Ly |

Man

166

DOW

|

|

SS

eae

ee

i

|

Rib

Femur

| Vertebra®)

(
|

—
—
—

1.1
—
—

9

»1
>1
1

|

1.3
0.8
—

0.53

O45
—

|

|

we ee

2.7

—

—

Ra /eTh|

28TH/28Ro
—— |

—

»>1

TH2 ' 22m © Long bones
THA | 12m ‘© Long bones;
TH5 » 22m | Long bones

ee os

Weighted|

38d
, 26d
, 48d

2284¢-/228Ra

ne

Lib!

Po
|
;

00940

means

Feuruinrium Activity Ratios or Trortum Davestern Propucts 1x Bone

|

—

|
|

1.16
1.03

|
|

1.8
1.16
1.06

|
|

|

—

L4

|
|
|
|

1.0

|

1.4

-—
-—

1.0
—
—

2.2
—
—

1.3
1.6
1.6

0.9

~1.0

—

0.8
1.1
1.3

1.3

—

0.9

|

212 Bi /:

|

|

—
—
—

—

22 Ph /24Ra

—

1.7
—

1.8

~

—

—

0.8
|

0.7
0.7
1

|

—

——}

~1

~I]
~

—

-

—

0.9

———_--

1

2) Containing bone marrow.

Caleulation based on an assumed 2%Th/2%Ra activity ratio of 1.00.

would be expected that manyof them, and particularly

“SRa, would be translocated to other organs or exereted. Since all the decay products are ultimately
derived from 7°*Th or **°Th located within the particulate phase, there is no problem in explaming the
fact that some of these decay-produet atoms are physically confined «within the particles. What does require
an explanation, however, is the inference from the biological data that not all the decay-product atoms remain bound with the “8“Th in this way. It is probably

significant in this connection that in experiments with

Thorotrast samples fron: the same hatch but in different animals and for different durations of the burden,
the 7*8Ra/*8°Th ratios reported for the RES cover
rather a narrow range of values (see for example Tables 42 and 43, batch 13098). The “retention” of 7*8Ra
therefore appears to be a property of the Thorotrast
itself rather than the animal.

A plausible mechanismfor the escape of radioactive

daughter products from the Thorotrast particles might
be thought to be diffusion. However, the physical halfhfe of a radionuchde would then be one of the most
important parameters determining its fractional retention. Consideration of the available biological data
for cach thorium daughter product in relation to its
physical half-life, renders this possibility unlikely (see
Table 50). Particularly this is evident in the case of
the two radium isotopes. *“*Ra (half-life 5.8 years;
fractional retention at late times in the particles of the
RES ~0.45) and *7*Ra (half-life 3.6 davs; fractional
retention in the particles of the RES ~0.7), since a

diffusion mechanism would require the fraction
tention to depend on the inverse square root |

half-life.
A more plausible mechanism predicts that dai
products can escape from the particles by virtue
recoil energy which they gain at the momento1
creation.'**) In the case of those nuclides whic

formed concurrently with the emission of an @ ra\
the parent nucleus, this recoil] energy is consid.

(Table 47). By the application of standard 1

energy relationships for heavy nuclei‘?3% it ¢
calculated that a **8Ra atom, for example, has

coil range of approximately 60 A in ThOs. Th

portant consideration now is whether this 1s shlong compared with the size of Thorotrast pai

From measurements of eleetron micrographsit ay

that the particle size is not closely controlled, for
been variously reported as 30 to 100 A with a mi

70 A, 80 to 200 A, and 55 + 25 A.*)

Nevertheless, these are of the same order of n
tude as the calculated recoil ranges of several :

thorium decay products, and it is, therefore, to |
pected that a substantial proportion of these

would be able to escape from the particulate ph
the Thorotrast. In the case of atoms formed by

transitions, the recoil range is very much lower.

ertheless, the recoil energy commonly exceedrequired for breaking chemical bonds (1-3 eV
would thus be sufficient to allow some of the atc
surface locations on the particles to break free, ¢
the change in chemical state alone were not suf

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