ESR imaging on a solid-tumor-bearing mouse using spin-labeled dextran

被引:10
|
作者
Saito, K [1 ]
Kazama, S
Tanizawa, H
Ito, T
Tada, M
Ogata, T
Yoshioka, H
机构
[1] Univ Shizuoka, Sch Pharmaceut Sci, Inst Environm Sci, Shizuoka 4228526, Japan
[2] Yamagata Univ, Grad Sch Engn, Yonezawa, Yamagata 9928510, Japan
关键词
ESR imaging; dextran; tumor; TEMPO; spin probe;
D O I
10.1271/bbb.65.787
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Imaging of a tumor with ESR was tried using two different types of spin probes, a Low molecular weight spin probe, CPROXYL, and a polymer spin probe, TEMPO-DX. Spin probes were administered to a mouse bearing a solid tumor that was a transplanted Ehrlich's ascites carcinoma in the back, using two methods, conventional intraperitoneal injection and continuous intravenous injection with a micro-feeder. First, the accumulation of the probe was examined by X-band ESR. CPROXYL, which was administered to a mouse intraperitoneally, was exclusively retained in urine, showing that it was rapidly excreted into the bladder, while TEMPO-DX was absorbed from the peritoneal cavity with difficulty to the vessel. Using continuous intravenous injection, CPROXYL was also rapidly excreted, but it was confirmed that TEMPO-DX concentrated in tumor tissue because it has a long half-life in vivo. In addition, measurement of E;SR imaging was done to measure the distribution of spin probes with continuous intravenous injection. The strongest spot of CPROXYL was observed on ESR images, showing the accumulation at the bladder, while the spot of TEMPO-DX was observed in the solid tumor of the basic of the mouse. These results suggest that TEMPO-DX could stay much longer than a low molecular weight spin probe in vivo and concentrate at the tumor. TEMPO-DX may be useful for developing specific ESR imaging agents for tumor.
引用
收藏
页码:787 / 794
页数:8
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