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1. 卫生部核医学重点实验室,江苏省原子医学研究所
2. 江南大学化工学院
纸质出版日期:2008-03-01
移动端阅览
[1]谭成,俞惠新,林秀峰,张莉,陈波,宋翠翠,曹国宪.碘标延胡索乙素及其小鼠体内分布[J].核技术,2008(03):219-222.
TAN Cheng1 YU Huixin1, 2 LIN Xiufeng1 ZHANG Li1 CHEN Bo1 SONG Cuicui2 CAO Guoxian1 1. Radioiodine-labeling of tetrahydropalmatine and its biodistribution in mice[J]. Nuclear techniques, 2008, (3): 219-222.
本文通过131I标记延胡索乙素(THP)以探讨其在小鼠体内的分布代谢。采用氯胺-T法对THP进行131I标记;以三氯甲烷萃取
聚酰胺薄膜为介质、正己烷:三氯甲烷:甲醇:醋酸=2:3:0.5:0.055(V/V)为展开剂
测定标记物的标记率和放化纯;KM小鼠尾静脉注射131I-延胡索乙素(185kBq/只
n=6)
分别于注射后5、10、30、60、120、240、1440min取各脏器、及脑部额叶、顶叶、枕叶、海马、纹状体、丘脑和血
称重、计数
计算每克组织百分注射剂量率(%ID·g-1)。结果表明
131I-延胡索乙素标记率达76%
纯化后其放化纯为97.3%
7和20天后分别为95.4%、96.8%;动物实验显示131I-延胡索乙素在小鼠体内广泛分布
主要经肝和肾进行代谢
5min时%ID·g-1分别为14.35、6.55
脂肪和肠也有较高分布
5min时ID·g-1分别为3.05、3.91;脑组织中5~10min即达峰值
各脑区均有分布
其中以顶叶、额叶和小脑略高
2h后脑中基本代谢完毕。由此可见
碘标延胡索乙素标记物稳定
体内主要经肝肾代谢
脂肪及脑内各区域也有较高分布
可用于进一步的微量示踪研究。
The work was to investigate radioiodinated tetrahydropalmatine and its biodistribution in mice. Tetrahy-dropalmatine was labeled with 131I using the chloramine-T method and the labeled compound were characterized by polyamide TLC. The animals were sacrificed at different times after radiopharmaceutical i.v. administration. The interested tissues samples were collected
and percent injected dose per gram (%ID·g-1) was calculated for each sample. The labeling yield of 131I-tetrahydropalmatine was 76% and its RCPs were 97.3%
95.4%
and 96.8% after 1
7 and 20 days
respectively. Biodistribution in mice demonstrated that 131I-tetrahydropalmatine was extensive
and it was me-tabolized mainly in liver and kidney
which contained of 14.35% and 6.55% ID·g-1at 5 min
respectively
with 3.26% and 1.20% ID·g-1at 4h
respectively. Comparatively high 131I-tetrahydropalmatine was found in intestine and fat
but clearance was slow
3.91%and 3.05% at 5 min and decreased to 0.79% and 0.37% at 4 h. The results also showed that 131I-tetrahydropalmatine could well penetrate the blood-brain barrier to attain a maximal level in brain tissue within 5~10 min
but it mostly was cleaned out after 2 h. There was no significant difference in brain regions despite of highest biodistribution in parietal lobe. In conclusion
131I-tetrahydropalmatine was stable and it was metabolized mainly in liver and kidney
but there was no significant difference in brain regions.
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