Abstract
The purpose of this study is to synthesize 123I-labeled hesperetin and to investigate its in vivo behavior. The optimized labeling condition provided two isomers of 123I-labeled hesperetin with high radiochemical yields and radiochemical purities. Both 123I-labeled products were orally administered to normal ICR mice, and the initial result showed that most of 123I activity was detected in the stomach and the intestines. A part of 123I-labeled hesperetin was absorbed from the small intestine to bloodstream and then it was distributed in normal organs. The results in the present study provided an efficient radiolabeling method of flavonoid and quantitative organ distribution of orally administered hesperetin.
Original language | English |
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Pages (from-to) | 437-443 |
Number of pages | 7 |
Journal | Journal of Radioanalytical and Nuclear Chemistry |
Volume | 306 |
Issue number | 2 |
DOIs | |
State | Published - 1 Nov 2015 |
Keywords
- Biodistribution
- Hesperetin
- Radiolabeling
- SPECT/CT