The pinhole SPECT for animal model of bone metastasis with SPC-A-1BM human pulmonary adenocarcinoma bone metastasis cell line

The study was to investigate the role of pinhole single photon emission computed tomography (SPECT), the human pulmonary adenocarcinoma bone-seeking metastasis cell line SPC-A-1BM was used. These cells form typical osteolytic bone metastases when inoculated into the arterial circulation of NIH-Beige...

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Veröffentlicht in:Nuclear science and techniques 2008-10, Vol.19 (5), p.290-296
Hauptverfasser: GAO, Xiuli, YANG, Shunfang, YU, Yongli, SHI, Meiping, ZHAO, Lanxiang, YE, Jianding, LU, Jianying
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Sprache:eng
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Zusammenfassung:The study was to investigate the role of pinhole single photon emission computed tomography (SPECT), the human pulmonary adenocarcinoma bone-seeking metastasis cell line SPC-A-1BM was used. These cells form typical osteolytic bone metastases when inoculated into the arterial circulation of NIH-Beige-Nude-XD (BNX) mice v/a the left ventricle. In order to evaluate the irradiation impact of ^99mTc-MDP versus X-ray on cells growth, we used six groups of SPC-A-IBM cells in our imaging scheme and irradiated by various doses of ^99mTc-MDP (37, 74, 111, 370, 740 MBq) and X-ray(40 kV, 2 mA, 6 s) respectively. The cell's number of each group was well recorded in different exposure time( 4, 8, 12, 24, 48, 72, 96 hours ). After that, SPC-A-1BM cells (1×106) were inoculated into the mice via left ventricle. We compared the results obtained with those different doses of ^99mTc-MDP using pinhole SPECT and conventional X-ray skeletal surveys. The data show that the cell-survival number of 111 MBq group has insignificant difference with that of X-ray and the dose is adequate to have an ideal image. Besides, it is important that the chromosome of the cells in the group of 111 MBq showed no irradiation-related damages in our test. These results implied that ^99mTc-MDP pinhole SPECT may provide another way other than conventional X-ray skeletal surveys in detecting bone metastasis of pulmonary adenocarcinoma in BNX mice.
ISSN:1001-8042
2210-3147
DOI:10.1016/S1001-8042(09)60006-3