G. Gartshore et al., EVALUATION OF TC-99M EXAMETAZIME STABILIZED WITH COBALT CHLORIDE AS ABLOOD-FLOW TRACER IN FOCAL CEREBRAL-ISCHEMIA, European journal of nuclear medicine, 21(9), 1994, pp. 913-923
A protocol has been devised to effectively ex tend the limited post-re
constitution shelf life of technetium-99m exametazime as a radiopharma
ceutical for imaging cerebral blood flow (CBF) distribution. The poten
tial of Tc-99m-exametazime stabilised with cobalt chloride for imaging
CBF distribution as late as 4 h after reconstitution has been examine
d in ischaemic and nonischaemic tissue in halothane-anaesthetised cats
. Focal cerebral ischaemia was produced by permanent middle cerebral a
rtery occlusion. The relationship between Tc-99m-exametazime uptake an
d retention and CBF (assessed with [C-14]iodoantipyrine 10 min after f
irst radiopharmaceutical administration) was determined in the same ti
ssue section with double label autoradiography. Over the CBF range 0 -
80 ml 100 g(-1) min(-1), the uptake of Tc-99m-exametazime (quantitati
vely and topographically) was linearly related to CBF irrespective of
whether the Tc-99m-labelled tracer was unstabilised (and administered
within 10 min of reconstitution) or was stabilised with cobalt chlorid
e (and administered up to 240 min after reconstitution). For levels of
CBF in excess of 80 mi 100 g(-1) min(-1) the excellent topographical
relationship between Tc-99m-exametazime distribution and CBF is mainta
ined but quantitatively, Tc-99m-exametazime underestimates CBF to a si
milar degree in animals receiving stabilised and unstabilised Tc-99m-e
xametazime. The presence of the stabiliser, cobalt chloride, extends g
reatly the period over which Tc-99m-exametazime can be used after reco
nstitution to generate images of CBF distribution in normal and ischae
mic cerebral tissue.