Technetium-99m labelled human serum albumin for ventriculography : a comparative evaluation of six labelling kits

• Published in: European Journal of Nuclear Medicine 1993-06, Vol.20 (6), p.465-472
• Main Authors: VANBILLOEN, H. P, VERBEKE, K. A, DE ROO, M. J, VERBRUGGEN, A. M
• Format: Article
• Language: English
• Subjects: Animals; Biological and medical sciences; Contrast media. Radiopharmaceuticals; Humans; Medical sciences; Mice; Pharmacology. Drug treatments; Rabbits; Radionuclide Ventriculography; Reagent Kits, Diagnostic; Technetium Tc 99m Aggregated Albumin - blood; Technetium Tc 99m Aggregated Albumin - pharmacokinetics; Tissue Distribution
• ISSN: 0340-6997; 1619-7089
• DOI: 10.1007/BF00175158

In this study we have compared the characteristics of six labelling kits for the preparation of technetium-99m labelled human serum albumin (99mTc-HSA) and evaluated the usefulness of the various 99mTc-HSA preparations as blood pool tracer agents. The amount of the principal ingredients, i.e. HSA and stannous ions, varies largely between the studied kits and this is probably a reason for the observed differences in the labelling rate. Analysis of the reaction mixtures after labelling of the respective kits with 99mTc showed in each preparation the presence of four to five radioactive components in variable relative amounts. The retention time of the main component on size-exclusion high-performance liquid chromatography (SEC-HPLC) was identical for all preparations. Biodistribution of the HPLC-isolated fractions was studied in mice. The components with the shortest and longest retention times on HPLC show poor retention in the plasma. The three intermediate fractions, including the principal peak, are initially retained relatively well in the blood (60%-70% of the injected dose after 10 min), but clearly to a lower degree than iodine-125 labelled HSA. Moreover, they diffuse out of the vascular compartment at a much higher rate than 125I-HSA. The biological behaviour of the main component of the various preparations was clearly different, despite the identical retention time on SEC-HPLC. Study of the total preparations in mice and a rabbit showed that two of them are cleared rapidly from the blood and cannot be considered valuable blood pool tracers. Diffusion of the other preparations out of the blood is slower but also considerable and compromises their use for ventriculography.