Journal
JOURNAL OF RADIOANALYTICAL AND NUCLEAR CHEMISTRY
Volume 317, Issue 3, Pages 1243-1252Publisher
SPRINGER
DOI: 10.1007/s10967-018-6013-z
Keywords
Doxorubicin; Radioidination; Tumor imaging; Molecular dynamics; Molecular docking
Funding
- Westgrid
- Compute/Calcul Canada
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Non-invasive molecular imaging techniques are accruing more interest in the last decades. Several radiolabelling elements have been FDA-approved and are currently used to characterize tumors. In this study, the DNA intercalating agent doxorubicin was radiolabelled with I-125. Several parameters for the radiolabelling reaction were investigated and optimized. A maximum yield of 94 +/- 0.3% was reached after reacting 20 mu g of doxorubicin with 200 mu g Chloramine-T at pH 5 for 30 min. The in vivo stability of I-125-doxorubicin is validated by the low propensity for thyroid uptake in mice. The preclinical T/NT ratio was approximately 6.4 at 30 min. Docking and molecular dynamics confirmed that the radiolabelling of doxorubicin did not affect (or slightly improved its binding to DNA). Overall, I-125-doxorubicin was demonstrated to be a promising non-invasive probe for solid tumor imaging. [GRAPHICS] .
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