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The Journal of Nuclear Medicine Vol. 11 No. 2 85-88
© 1970 by Society of Nuclear Medicine
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Compartmental Redistribution of 99mTc-Pertechnetate in the Presence of Perchlorate Ion and its Relation to Plasma Protein Binding

William H. Oldendorf, Warden B. Sisson and Youichi Iisaka

Wadsworth Hospital, Veterans Administration Center, Los Angeles, California
UCLA School of Medicine, Los Angeles, California

Correspondence: For reprints contact: William H. Oldendorf, Veterans Administration Center, Wilshire and Sawtelle Blvds., Los Angeles, Calif. 90073.

ABSTRACT

It was shown in rabbits that the addition of 3 mg/kg of perchlorate (ClO4) ion results in a major tissue redistribution of pertechnetate (TcO4). This probably results from (1) release of TcO4 from plasma protein binding sites with resulting redistribution to tissue extracellular spaces and (2) a shift of a portion of the TcO4 intracellularly. The injection of this dose of ClO4 results in tissue levels relative to blood plasma about 1.38 times greater than without ClO4.

In the presence of ClO4,, TcO4 moves from plasma into red cells. The ClO4 dose dependence of this plasma-to-red cell shift was studied in vivo. The ratio of plasma-to-red cell concentration of TcO4 shifts from 3.98 ± 0.3 1 without ClO4 to 1.98 ± 0.32 with 3 mg/kg of ClO4. This intracellular shift was demonstrated in vitro at a single high concentration of ClO4 producing a ratio of 1.25.

The effect of ClO4 on plasma-to-red cell distribution is complete within 1 min of i.v. injection in the rabbit.

Chloride does not redistribute between red cellsand plasma as does TcO4 in response to ClO4.

Preliminary dialysis studies indicate about 80% of plasma TcO4 is protein bound in rabbit and man. This drops to about 40% in the presence of ClO4 concentrations used in this study in the rabbit but changes very little in man.

The tissue compartmental redistribution in the presence of ClO4 described here is not expected to produce visible changes in clinical scan appearance except in those organs where active uptake is present.

Possible mechanisms responsible for this redistribution are discussed.







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Copyright © 1970 by the Society of Nuclear Medicine.