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 language | English |
|---|---|
| Article number | e54759 |
| Journal | Journal of Visualized Experiments |
| Volume | 2016 |
| Issue number | 116 |
| DOIs | |
| State | Published - 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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