Abstract | PURPOSE: The aim of this study is to synthesize and evaluate (68)Ga-labeled Lissamine Rhodamine B (LRB) as a new radiotracer for imaging MDA-MB-231 and MCF-7 cells induced tumor mice by positron emission tomography (PET). METHODS: Firstly, we performed the radio synthesis and microPET imaging of (68)Ga(DOTA-LRB) in athymic nude mice bearing MDA-MB-231 and MCF-7 human breast cancer xenografts. Additionally, the evaluations of (18)F-fluorodeoxyglucose (FDG), as a glucose metabolism radiotracer for imaging tumors in the same xenografts, have been conducted as a comparison. RESULTS: The radiochemical purity of (68)Ga(DOTA-LRB) was >95%. MicroPET dynamic imaging revealed that the uptake of (68)Ga(DOTA-LRB) was mainly in normal organs, such as kidney, heart, liver, and brain and mainly excreted from kidney. The MDA-MB-231 and MCF-7 tumors were not clearly visible in PET images at 5, 15, 30, 40, 50, and 60 min after injection of (68)Ga(DOTA-LRB). The tumor uptake values of (18)F-FDG were 3.79 ± 0.57 and 1.93 ± 0.48%ID/g in MDA-MB-231 and MCF-7 tumor xenografts, respectively. CONCLUSIONS: (68)Ga(DOTA-LRB) can be easily synthesized with high radiochemical purity and stability; however, it may be not an ideal PET radiotracer for imaging of MDR-positive tumors.
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Authors | Xuena Li, Yafu Yin, Bulin Du, Na Li, Yaming Li |
Journal | BioMed research international
(Biomed Res Int)
Vol. 2016
Pg. 8549635
( 2016)
ISSN: 2314-6141 [Electronic] United States |
PMID | 26949707
(Publication Type: Journal Article, Research Support, Non-U.S. Gov't)
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Chemical References |
- Contrast Media
- Radiopharmaceuticals
- Rhodamines
- Fluorodeoxyglucose F18
- lissamine rhodamine B
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Topics |
- Animals
- Breast Neoplasms
(diagnostic imaging, metabolism, pathology)
- Contrast Media
(chemical synthesis, pharmacology)
- Fluorodeoxyglucose F18
(pharmacology)
- Humans
- MCF-7 Cells
- Mice
- Positron-Emission Tomography
(methods)
- Radiopharmaceuticals
(pharmacology)
- Rhodamines
(chemical synthesis, pharmacology)
- Tissue Distribution
- Xenograft Model Antitumor Assays
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