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Title: Technetium-99m-human polyclonal IgG radiolabeled via the hydrazino nicotinamide derivative for imaging focal sites of infection in rats

Journal Article · · Journal of Nuclear Medicine; (USA)
OSTI ID:5987730

The biologic behavior of human polyclonal immunoglobulin (IgG) radiolabeled with technetium-99m ({sup 99m}Tc) by a novel method, via a nicotinyl hydrazine derivative, was evaluated in rats. Technetium-99m- and indium-111-IgG were co-administered to normal rats and biodistribution was determined at 2, 6, and 16 hr. The inflammation imaging properties of the two reagents were compared in rats with deep-thigh infection due to Escherichia coli. Blood clearance of both antibody preparations was well described by a bi-exponential function: ({sup 99m}Tc-IgG: t1/2 = 3.82 +/- 0.89 and 57.52 +/- 1.70 hr. {sup 111}In-IgG: 3.93 +/- 0.117 and 40.71 +/- 1.26 hr). Biodistributions in the solid organs were similar, however, small but statistically significant differences were detected: {sup 99m}Tc-IgG greater than {sup 111}In-IgG in lung, liver, and spleen; {sup 99m}Tc-IgG less than {sup 111}In-IgG in kidney and skeletal muscle (p less than 0.01). At all three imaging times, target-to-background ratio and percent residual activity for the two compounds were remarkably similar. These studies establish that human polyclonal IgG labeled with {sup 99m}Tc via a nicotinyl hydrazine modified intermediate is equivalent to {sup 111}In-IgG for imaging focal sites of infection in experimental animals.

OSTI ID:
5987730
Journal Information:
Journal of Nuclear Medicine; (USA), Vol. 31:12; ISSN 0161-5505
Country of Publication:
United States
Language:
English

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