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Physico-chemical study of the radiopharmaceuticals 99mTc-DMSA, 99mTc-EDTA and 99mTc-DTPA interaction with plasmatic proteins.

作者信息

Garcia Domenech R, Abril Mendez O, Galvez Alvarez J, Farga Marti A

机构信息

School of Pharmacy, Department of Chemical Physics, University of Valencia, Spain.

出版信息

Int J Rad Appl Instrum A. 1989;40(6):536-8. doi: 10.1016/0883-2889(89)90141-x.

DOI:10.1016/0883-2889(89)90141-x
PMID:2551850
Abstract

This report studies the binding rate of the radiopharmaceuticals 99mTc-DTPA, 99mTc-EDTA and 99mTc-DMSA to plasmatic proteins. The proteins bind to the tested radiopharmaceuticals in the following sequence: 99mTc-DTPA less than 99mTc-DMSA(C1) less than 99mTc-EDTA less than 99mTc-DMSA(C2) where C1 and C2 represent two different Tc-DMSA complexes. The thermodynamic study suggests a quantitative relationship of radiopharmaceutical:protein = 1:1 and an almost nonexistent influence of the temperature, which means that the interacting forces in this process are relatively weak.

摘要

相似文献

1
Physico-chemical study of the radiopharmaceuticals 99mTc-DMSA, 99mTc-EDTA and 99mTc-DTPA interaction with plasmatic proteins.
Int J Rad Appl Instrum A. 1989;40(6):536-8. doi: 10.1016/0883-2889(89)90141-x.
2
Stability of the radiopharmaceutical [99mTc]DMSA: study of the ligand exchange reaction with [99Tc]EDTA.放射性药物[99mTc]二巯基丁二酸的稳定性:与[99Tc]乙二胺四乙酸配体交换反应的研究
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