Chinese Clinical Oncology
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ZHANG Tao, ZHOU Nai-kang, ZHANG Jin-ming, MA Yong-fu
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Abstract: Objective To investigate the biodistribution of a new PET tracer—11Cpodophyllotoxin(11C-PDT) in mice model of lung carcinoma and inflammation, and the value of 11C-PDT to differentiate the two models. Methods The biodistribution of 11C-PDT was performed in mice model,and 18F-FDG was used as control. Twelve mice with lung carcinoma and twelve mice with inflammation were divided into two groups according to the different tracers at random. 11C-PDT or 18F-FDG was injected into coccygeal vein of mice model. The biodistribution of mice for 11C-PDT and 18F-FDG were measured with wellgamma detector at 60 min after injection. Results On the biodistribution study of 11C-PDT,the radioactive uptake(%ID/g) in tumor was higher than that in the inflammation tissue(0.63±0.25 vs. 0.29±0.09,P<0.05);the radioactive uptake(%ID/g)of 18F-FDG in tumor was also higher than that in the inflammation tissue(7.56±1.77 vs. 3.83±0.71,P<0.01). The uptake between 11C-PDT and 18F-FDG in tumor was of significance(P<0.05). The ratios of inflammation/muscle of 18F-FDG(1.58±0.11)were higher than those of 11C-PDT(0.73±0.28)with statistic significance(P<0.05). Conclusion11C-PDT is more specific than 18F-FDG in tumor tissue, and could be used as PET tracer to differatiate lung carcinoma from inflammation in the future.
ZHANG Tao, ZHOU Nai-kang, ZHANG Jin-ming, MA Yong-fu. Differential diagnostic value of 11Cpodophyllotoxin as a PET tracer on lung carcinoma and inflammation[J].Chinese Clinical Oncology, 2012, 17(10): 865-.
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http://manu65.magtech.com.cn/Jwk3_lczlxzz/EN/Y2012/V17/I10/865
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