journal article·2012-06-26

64Cu Core-Labeled Nanoparticles with High Specific ActivityviaMetal-Free Click Chemistry

Dexing Zeng, Nam S. Lee, Yongjian Liu, Dong Zhou, Carmen S. Dence, Karen L. Wooley, John A. Katzenellenbogen, Michael J. Welch

ACS Nano· Volume 6· Issue 6
Publisher page

Abstract

A novel strategy based on metal-free "click" chemistry was developed for the copper-64 radiolabeling of the core in shell-cross-linked nanoparticles (SCK-NPs). Compared with Cu(I)-catalyzed click chemistry, this metal-free strategy provides the following advantages for Cu-64 labeling of the core of SCK-NPs: (1) elimination of copper exchange between nonradioactive Cu in the catalyst and DOTA-chelated Cu-64; (2) elimination of the internal click reactions between the azide and acetylene groups in the same NPs; and (3) increased efficiency of the click reaction because water-soluble Cu(I) does not need to reach the hydrophobic core of the NPs. When 50 mCi Cu-64 was used for the radiolabeling, the specific activity of the radiolabeled product was 975 Ci/μmol at the end of synthesis, which represents the attachment of ca. 500 Cu-64 atoms per SCK-NP, giving in essence a 500-fold amplification of specific activity of the NP over that of the Cu-64 chelate. To the best of our knowledge, this is the highest specific activity obtained for Cu-64-labeled nanoparticles.
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Research context

OpenAlex topics: Click Chemistry and Applications · Chemical Synthesis and Analysis · Advanced biosensing and bioanalysis techniques

SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.

Affiliations

Mallinckrodt Institute of Radiology, Washington University School of Medicine, St. Louis, Missouri 63110, United States

Departments of Chemistry and Chemical Engineering, Texas A&M University, College Station, Texas 77842, United States

Department of Chemistry, University of Illinois at Urbana−Champaign, Urbana, Illinois 61801, United States

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