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Synthesis and Evaluation of an Enantiomerically Enriched Bifunctional Chelator for 64 Cu‐Based Positron Emission Tomography (PET) Imaging
Author(s) -
Chong HyunSoon,
Sun Xiang,
Zhong Yongliang,
Bober Kamil,
Lewis Michael R.,
Liu Dijie,
Ruthengael Varyanna C.,
Sin Inseok,
Kang Chi Soo
Publication year - 2014
Publication title -
european journal of organic chemistry
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.825
H-Index - 155
eISSN - 1099-0690
pISSN - 1434-193X
DOI - 10.1002/ejoc.201301499
Subject(s) - bifunctional , chelation , chemistry , biodistribution , positron emission tomography , in vivo , radiochemistry , stereochemistry , in vitro , combinatorial chemistry , nuclear chemistry , nuclear medicine , organic chemistry , biochemistry , medicine , microbiology and biotechnology , biology , catalysis
We report the synthesis and evaluation of an enantiomerically enriched bifunctional chelator, ( S )‐ C ‐NE3TA. The bifunctional chelator was efficiently prepared by regioselective and stereoselective ring opening of an aziridinium ion. The new chiral chelator instantly and almost completely bound to 64 Cu at room temperature. The corresponding 64 Cu‐radiolabeled complex remained intact in human serum for 48 h without any measurable transchelation and was tolerant to a rigorous EDTA challenge for 24 h. The 64 Cu‐radiolabeled ( S )‐ C ‐NE3TA complex was stable in mice and produced an excellent biodistribution profile. The results of the in vitro and in vivo evaluations indicate that the new optically active chelator is a promising candidate for PET imaging applications.