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An optimized protocol for the efficient radiolabeling of gold nanoparticles by using a125i-labeled azide prosthetic group

  • Jongho Jeon
  • , Ha Eun Shim
  • , Sajid Mushtaq
  • , Mi Hee Choi
  • , Sang Hyun Park
  • , Dae Seong Choi
  • , Beom Su Jang
  • Korea Atomic Energy Research Institute
  • University of Science and Technology UST

Research output: Contribution to journalArticlepeer-review

6 Scopus citations

Abstract

Here, we demonstrate a detailed protocol for the radiosynthesis of a125I-labeled azide prosthetic group and its application to the efficient radiolabeling of DBCO-group-functionalized gold nanoparticles using a copper-free click reaction. Radioiodination of the stannylated precursor (2) was carried out by using [125I]NaI and chloramine T as an oxidant at room temperature for 15 min. After HPLC purification of the crude product, the purified125I-labeled azide (1) was obtained with high radiochemical yield (75 ± 10%, n = 8) and excellent radiochemical purity (>99%). For the synthesis of radiolabeled 13-nm-sized gold nanoparticles, the DBCO-functionalized gold nanoparticles (3) were prepared by using a thiolated polyethylene glycol polymer. A copper-free click reaction between 1 and 3 gave the125I-labeled gold nanoparticles (4) with more than 95% of radiochemical yield as determined by radio-thin-layer chromatography (radio-TLC). These results clearly indicate that the present radiolabeling method using a strain-promoted copper-free click reaction will be useful for the efficient and convenient radiolabeling of DBCOgroup-containing nanomaterials.

Original languageEnglish
Article numbere54759
JournalJournal of Visualized Experiments
Volume2016
Issue number116
DOIs
StatePublished - 10 Oct 2016

Keywords

  • Azide
  • Bioorthogonal reaction
  • Chemistry
  • Copper-free click reaction
  • Gold nanoparticles
  • Issue 116
  • Prosthetic group
  • Radioactive iodine
  • Radioisotope
  • Radiolabeling
  • Radiotracer

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