Title of article
Preclinical Evaluation of 68Ga-MAA from Commercial Available 99mTc- MAA Kit
Author/Authors
Shanehsazzadeh, Saeed Radiation Application Research School - Nuclear Science and Technology Research Institute (NSTRI), Tehran, Iran , Jalilian, Amir Reza Radiation Application Research School - Nuclear Science and Technology Research Institute (NSTRI), Tehran, Iran , Lahooti, Afsaneh Department of Medical Physics and Biomedical Engineering - Faculty of Medicine - Tehran University of Medical Science, Iran , Geramifar, Parham Research Center for Nuclear Medicine - Shariati Hospital - Tehran University of Medical Sciences, Tehran, Iran , Beiki, Davood Research Center for Nuclear Medicine - Shariati Hospital - Tehran University of Medical Sciences, Tehran, Iran , Yousefnia, Hassan Radiation Application Research School - Nuclear Science and Technology Research Institute (NSTRI), Tehran, Iran , Rabiee, Amir Radiation Application Research School - Nuclear Science and Technology Research Institute (NSTRI), Tehran, Iran , Mazidi, Mohammad Radiation Application Research School - Nuclear Science and Technology Research Institute (NSTRI), Tehran, Iran , Mirshojaei, Fatemeh Radiation Application Research School - Nuclear Science and Technology Research Institute (NSTRI), Tehran, Iran , Maus, Stephan Clinic of Nuclear Medicine - University Medical Centre Mainz - Langenbeckstrasse 1, D-55131 Mainz, Germany
Pages
9
From page
1415
To page
1423
Abstract
99mTc-Macroaggregated Albumin (99mTc-MAA) has been used as a perfusion agent. This
study described development of the 68Ga-MAA via commercially available kits from Pars-
Isotopes Company as a 99mTc-MAA kit. 68Ge/68Ga generator was eluted with suprapure HCl
(0.6 M, 6 mL) in 0.5 mL fractions. The two fractions with the highest 68GaCl3 activity were
generally used for labeling purposes. After labeling, the final product was centrifuged 2 times to
purify the solution. Five rats were sacrificed at each exact time interval (from 15 min to 2 h post
injection) and the percentage of injected dose per gram (%ID/g) of each organ was measured by
direct counting from 11 harvested organs of rats. The RTLC showed that labeling yields before
centrifuges were 90% and 95% for Pars-Isotopes and GE kits, respectively and after centrifuges,
they became 100%. The microscopic size examination showed a shift in the particle sizes post
centrifuges and the biodistribution data revealed the efficiency and benefits of centrifuges in
terms of preventing the of liver and bone marrow uptakes especially for Pars-Isotopes kits. Our
results showed that after centrifuges of the final product, the lung uptakes increased from 89%
to more than 97% of %ID/g after 5 min post injections. The whole procedure took less than 25
min from elution to the final product. Since 99mTc-MAA remained longer than 68Ga-MAA in the
lung and 68Ga-MAA showed better image qualities, using 68Ga-MAA is recommended.
Keywords
pulmonary ventilation/perfusion scan , Imaging , 68Ga , Macroaggregated Albumin , Biodistribution
Journal title
Astroparticle Physics
Serial Year
2017
Record number
2416496
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