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作 者:万卫星[1] 张荣军[1] 谭成[1] 蔡刚明[1] 范益军 季顺东[2] 韩玉珉[3] 金坚[1]
机构地区:[1]核医学国家重点实验室,江苏省原子医学研究所,214063 [2]苏州医学院血栓与止血研究室 [3]中国科学院生物物理研究所
出 处:《中华核医学杂志》1999年第4期201-203,共3页Chinese Journal of Nuclear Medicine
摘 要:目的 探讨以凝血酶为靶,重组水蛭素(rH)为配基进行血栓显像的潜在价值。方法 氯胺T法制备125IrH,采用体外放射配体结合法分析rH对凝血酶纤维蛋白复合物的亲和、定量关系和时间反应动力学。亚氨基噻吩盐酸盐修饰法制备99TcmrH,进行小鼠体内分布测定及犬动、静脉血栓模型显像。结果 rH 不能直接与纤维蛋白原结合,当凝血酶与纤维蛋白形成复合物后才能与其形成三元复合物,且这种结合呈高亲和、特异和可逆性。99TcmrH 在小鼠心、脑、肝、脾、肺摄取低,肾摄取高,15 min 达(64-724±5-042) %ID/organ,血清除迅速。犬股动脉血栓于45 min 可清晰显影,靶/ 本底(T/B) 比值为1-47。静脉血栓于注药后30 min 就出现浓聚,并随时间延长血栓显影更清晰,1 h T/B比值为1-53。结论 99TcmrH 有望成为1Objective To assessthe ability ofthe directthrombin (Th) inhibitor,recombinant hirudin (rH) as a new thrombusimagingligand- Methods 125I rHwas prepared by chloramine Tmethod,99Tcm rHby modified 2 iminothiolane method- The affinity ofrHto Th fibrin complex wasanalyzed bythecompetitiveradioas sayin vitro,the kinetics ofthe rH Th fibrin complex formation was studied too- Biodistribution of 99Tcm rHin mice wasdetermined andthrombusimaging was performedin dogthrombosis model- Results TherHcould only bind with Th fibrin complex,butnotdirectly withfibrinogen andthe binding wasoffairly high specificity and a vidity- The biodistribution studyin mice demonstrated thatrH was excreted from kidneys [(64-724 ±5-042)% ID/orgen within 15 min afterinjection] and there waslow uptakein heart,brain,liver,spleen and lungs- In SPECTimaging,allthrombi were clearly visible,arterialthrombi were seen clearly within 45 min afterinjection (T/B= 1-47) andfadedawayslowly,venousthrombi werealsoseen within30 minafterinjection and quantitative imagingratios ofthethrombustothe contralateralvesselincreased withtime (T/B= 1-53in 60 min)- Conclu sions Allthese resultsindicatethatTh probablycan beregarded asthetargetor markerin diagnosisofthrombus formation and rHcan be used asa newligandinthrombusimaging-
分 类 号:R817.42[医药卫生—影像医学与核医学]
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