Evaluation of 99Tcm-labelled human immunoglobulin in animal models of experimentally induced inflammatory lesions

1995 ◽  
Vol 16 (10) ◽  
pp. 846-852 ◽  
Author(s):  
H. H. SHIMPI ◽  
O. P. D. NORONHA ◽  
A. M. SAMUEL
Brain ◽  
2008 ◽  
Vol 131 (3) ◽  
pp. e92-e92 ◽  
Author(s):  
B. Brochet ◽  
V. Dousset ◽  
M. Deloire ◽  
C. Boiziau ◽  
K. G. Petry

1996 ◽  
Vol 22 (12) ◽  
pp. 635-637 ◽  
Author(s):  
Mutsumi Miyauchi ◽  
Takashi Takata ◽  
Hiroshi Ito ◽  
Ikuko Ogawa ◽  
Joji Kobayashi ◽  
...  

2002 ◽  
Vol 87 (03) ◽  
pp. 374-382 ◽  
Author(s):  
Daniel Myers ◽  
Shirley Wrobleski ◽  
Frank Londy ◽  
Beverly Fex ◽  
Angela Hawley ◽  
...  

SummaryP-selectin antagonism decreases thrombosis and inflammation in animal models of venous thrombosis (VT) prophylaxis. This study defines results using a P-selectin receptor antagonist for VT treatment.Eight juvenile baboons underwent 6 h of iliofemoral venous stasis to produce an occlusive VT. Two days later, animals were treated for 14 days with rPSGL-Ig, 4 mg/kg (n3), LMWH (n2) or saline (n3) and treatment continued weekly (rPSGL-Ig) or daily (LMWH, saline). The animals were examined and sacrificed 14 days after treatment initiation (n4) or on day 90 (n4).Percent spontaneous vein reopening revealed a significant increase (p <0.05) in the proximal iliac vein in rPSGL-Ig and LMWH animals compared to controls (62%, 70% vs 8%), without differences in inflammation. No anticoagulation, thrombocytopenia, or wound complications were found in rPSGL-Ig animals. At 90 days, recanalization with iliac vein valve competence was found in treated animals.rPSGLIg successfully treated established VT without anticoagulation.


1991 ◽  
Vol 30 (01) ◽  
pp. 18-23 ◽  
Author(s):  
A. Saptogino ◽  
F. Wolf ◽  
W. Becker

Recently, polyclonal unspecific human immunoglobulin was suggested as a new agent for the localization of inflammatory lesions. Little information about the biodistribution of this radiopharmaceutical was reported so far. To obtain further information, 99mTc-labelled human immunoglobulin (HIG) was administered to a volunteer with presumed normal biokinetics. The absorbed doses to the organs were calculated according to the MIRD concept. The scintigraphic images at 1, 2, 4 and 24 h post injection demonstrated a prolonged activity retention in the blood and high activity in the kidneys, bladder and also in the liver. No significant uptake in the bowels and the marrow could be observed over the whole period of study. 27.4% of the administered activity was excreted in the urine within 24 h. The calculated organ absorbed doses, all in μGy/MBq, were estimated as follows: whole body 2.7, liver 7.3, spleen 12.0, kidneys 15.3, lungs 3.2, marrow 9.6 and gonads 17.0. From these results an effective dose equivalent of 7.9 • 10−3 mSv/MBq was calculated. The cancer risk estimate of 5 • 10−5, using 370 MBq 99mTc-HIG, may be considered quite low in comparison to other scintigraphic methods of diagnosing inflammation.


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