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(99)Tc(m)-N(NOEt)(2)在KMB17人胚肺二倍体细胞与不同种类肺癌细胞中的摄取动力学比较
BACKGROUND AND OBJECTIVE: PET/CT imaging is expensive, so searching the tumor imaging agent for SPECT/CT is necessary. (99)Tc(m)-N(NOEt)(2) [bis (N-ethoxy-N-ethyl dithiocarbamato) nitrido(99)Tc(m) (Ⅴ)] can be uptaken by lung cancer cells and other cells alike. The aim of this study is to evaluate th...
Formato: | Online Artículo Texto |
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Lenguaje: | English |
Publicado: |
中国肺癌杂志编辑部
2010
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6000428/ https://www.ncbi.nlm.nih.gov/pubmed/20677555 http://dx.doi.org/10.3779/j.issn.1009-3419.2010.04.07 |
Sumario: | BACKGROUND AND OBJECTIVE: PET/CT imaging is expensive, so searching the tumor imaging agent for SPECT/CT is necessary. (99)Tc(m)-N(NOEt)(2) [bis (N-ethoxy-N-ethyl dithiocarbamato) nitrido(99)Tc(m) (Ⅴ)] can be uptaken by lung cancer cells and other cells alike. The aim of this study is to evaluate the distinctive value in lung tumor with (99)Tc(m)-N(NOEt)(2), the difference in its uptake kinetics in human embryonic lung diploid fibroblasts KMB17 and several kinds of lung cancer cells lines. METHODS: Firstly, six different cell culture medium which contained YTMLC Gejiu human lung squamous carcinoma cell, SPC-A1 human lung adenocarcinoma cell, AGZY low metastatic human lung adenocarcinoma, 973 high metastatic human lung adenocarcinoma cell, GLC-82 Gejiu human lung adenocarcinoma cell, and KMB17 human embryonic lung diploid fibroblast, respectively with equal cell density of 1×10(6)/mL and the same volume were prepared; secondly, the same radioactive dose of (99)Tc(m)-N(NOEt)(2) was added into each sample and then 300 μL mixed sample was taken out respectively and cultured in 37 ℃ culture box; Finally, 5 min, 15 min, 30 min, 45 min, 60 min, 75 min, 90 min after cultivation, centrifuged each cultured sample and determined the intracellular radiocounts of each sample, calculated each cell sample's uptake rate of (99)Tc(m)N(NOEt)(2) at different time. RESULTS: Statistical difference was found among six cell samples, and the uptake rate sequence from high to low is 973 and SPC-A1 > YTMLC > GLC-82 > AGZY > KMB17 respectively; furthermore, 30 min-45 min after culture, the uptake rate reached stability, and the 45 min uptake rate of each sample was higher than its 96.7% uptake peak. CONCLUSION: Based on the results above mentioned, it is supposed that there are discriminative clinical value when using (99)Tc(m)-N(NOEt)(2) as a tumor targeting imaging agent, and 30 min or so after injection may be the best imaging time in the early imaging stage. |
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