Kazama S, Takashige G, Yoshioka H, Tanizawa H, Ogata T, Koscielniak J, Berliner L J
School of Pharmaceutical Sciences, University of Shizuoka, Japan.
Magn Reson Med. 1996 Oct;36(4):547-50. doi: 10.1002/mrm.1910360407.
The nitroxide group 2,2,6,6-tetramethylpiperidine-1-oxyl (TEMPO) was covalently bound to a dextran via an N-acetamido linkage to produce a novel spin probe, TEMPO-dextran (TEMPO-DX), which circulates for long time periods in an animal without metabolic degradation. TEMPO-DX was stable in mice, while small TEMPO analogs quickly disappeared after administration. Since dextran was reduced somewhat in size during synthesis, the resultant spin-labeled dextran could be excreted through the kidney. A strong L-band electron spin resonance signal was obtained shortly after intravenous administration of TEMPO-DX into the tail vein of a mouse, from which three-dimensional images of specific organs were calculated. The signal was found to persist for well over 1 h.
氮氧化物基团2,2,6,6 - 四甲基哌啶 - 1 - 氧基(TEMPO)通过N - 乙酰氨基键与葡聚糖共价结合,生成一种新型自旋探针,即TEMPO - 葡聚糖(TEMPO - DX),它能在动物体内长时间循环而不发生代谢降解。TEMPO - DX在小鼠体内稳定,而小分子TEMPO类似物给药后很快消失。由于合成过程中葡聚糖尺寸略有减小,所得的自旋标记葡聚糖可通过肾脏排泄。将TEMPO - DX经尾静脉静脉注射到小鼠体内后不久,就获得了强烈的L波段电子自旋共振信号,并据此计算出特定器官的三维图像。发现该信号能持续超过1小时。