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Preparation and Evaluation of [201Tl](Iii)-Dtpa-Higg for Inflammation Detection



Jalilian AR1 ; Khorrami A2 ; Tavakoli MB2 ; Kamalidehghan M1 ; Yari Kamrani YY1 ; Shahidi F3
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Authors Affiliations
  1. 1. Cyclotron and Nuclear Medicine Department, Nuclear Research Center for Agriculture and Medicine (NRCAM), Karaj, Iran
  2. 2. Medical Physics and Engineering Department, Isfahan University of Medical Sciences, Isfahan, Iran
  3. 3. Nuclear Electronic Department, Nuclear Research Center for Agriculture and Medicine (NRCAM), Karaj, Iran

Source: Iranian Journal of Radiation Research Published:2006

Abstract

Background: Radiolabeled polyclonal human immunoglubins are useful in the detection of inflammations. In this work a novel approach has been presented to use thallium-201 as a complexing nuclide for the development of radioimmuno-conjugates. Materials and Methods: Thallium-201 (T1/2=3.04 d) in TI+ form was converted to TI3+ cation in presence of O3 in 6M HCl, controlled by RTLC/gel electrophoresis methods and used in the labeling of human polyclonal antibody (HIgG) after residulation with freshly prepared cyclic DTPA-dianhydride. The best results of the conjugation were obtained by the addition of 1 mi of a HIgG pharmaceutical solution (5 mg/ml, in phosphate buffer, pH=7) to a glass tube, which was pre-coated with DTPA-dianhydride (0.01 mg) at 25°C with continuous mild stirring for 30 min. Results: The final isotonic [201TI](III)-DTPA-HIgG complex was checked by radio-TLC using several solvent systems to ensure the formation of only one species, and it was followed by filtration through a 0.22 μm filter (specific activity= 33.7 TBq/mM, radiochemical purity>95%). Preliminary bio-distribution studies in normal and inflammation-bearing rats were performed. The target/skin and target/ blood ratios were 4 and 6 after 28h, respectively, showing the selectivity of the radiopharmaceutical for the inflammatory lesions. Conclusion: The incorporation of TI(III) cation into a immunoconjugate was performed using the known methods. The biodistribution of the immunocomplex was shown to be consistent with a stable complex for the detection of inflammations. Significant inflammation detection was observed for the final complex in rats with turpentine oil-induced inflammation.
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