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New Bifunctional Chelator for Cu-64-Immuno-Positron Emission Tomography
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dc.contributor.author Pandya, Darpan N. -
dc.contributor.author Bhatt, Nikunj -
dc.contributor.author Dale, Ajit V. -
dc.contributor.author Kim, Jung Young -
dc.contributor.author Lee, Hochun -
dc.contributor.author Ha, Yeong Su -
dc.contributor.author Lee, Ji-Eun -
dc.contributor.author An, Gwang Il -
dc.contributor.author Yoo, Jeongsoo -
dc.date.available 2017-07-11T06:34:30Z -
dc.date.created 2017-04-10 -
dc.date.issued 2013-08 -
dc.identifier.issn 1043-1802 -
dc.identifier.uri http://hdl.handle.net/20.500.11750/3216 -
dc.description.abstract A new tetraazamacrocyclic bifunctional chelator, TE2A-Bn-NCS, was synthesized in high overall yield from cyclam. An extra functional group (NCS) was introduced to the N-atom of TE2A for specific conjugation with antibody. The Cu complex of TE2A-Bn-NCS showed high kinetic stability in acidic decomplexation and cyclic voltammetry studies. X-ray structure determination of the Cu-TE2A-Bn-NH2 complex confirmed octahedral geometry, in which copper atom is strongly coordinated by four macrocyclic nitrogens in equatorial positions and two carboxylate oxygen atoms occupy the elongated axial positions. Trastuzumab was conjugated with TE2A-Bn-NCS and then radiolabeled with 64Cu quantitatively at room temperature within 10 min. Biodistribution studies showed that the 64Cu-labeled TE2A-Bn-NCS-trastuzumab conjugates maintain high stability in physiological conditions, and NIH3T6.7 tumors were clearly visualized up to 3 days by 64Cu-immuno-positron emission tomography imaging in animal models. © 2013 American Chemical Society. -
dc.publisher American Chemical Society -
dc.title New Bifunctional Chelator for Cu-64-Immuno-Positron Emission Tomography -
dc.type Article -
dc.identifier.doi 10.1021/bc400192a -
dc.identifier.scopusid 2-s2.0-84883192247 -
dc.identifier.bibliographicCitation Pandya, Darpan N. (2013-08). New Bifunctional Chelator for Cu-64-Immuno-Positron Emission Tomography. Bioconjugate Chemistry, 24(8), 1356–1366. doi: 10.1021/bc400192a -
dc.subject.keywordPlus BRIDGED MACROCYCLIC CHELATORS -
dc.subject.keywordPlus IN-VIVO BEHAVIOR -
dc.subject.keywordPlus MONOCLONAL-ANTIBODIES -
dc.subject.keywordPlus COPPER-64 RADIOPHARMACEUTICALS -
dc.subject.keywordPlus BIOLOGICAL EVALUATION -
dc.subject.keywordPlus KINETIC INERTNESS -
dc.subject.keywordPlus IMMUNO-PET -
dc.subject.keywordPlus COMPLEXES -
dc.subject.keywordPlus CANCER -
dc.subject.keywordPlus DERIVATIVES -
dc.citation.endPage 1366 -
dc.citation.number 8 -
dc.citation.startPage 1356 -
dc.citation.title Bioconjugate Chemistry -
dc.citation.volume 24 -
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