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作 者:刘长滨[1] 徐白萱[1] 张锦明[1] 王瑞民[1] 关志伟[1] 姚树林[1] 田嘉禾[1]
出 处:《军医进修学院学报》2012年第4期382-386,共5页Academic Journal of Pla Postgraduate Medical School
基 金:教育部留学回国人员科研启动基金资助项目(030312)~~
摘 要:目的采用治疗性核素铼188(rhenium-188,188Re)标记Morpholino寡核苷酸,探讨其作为治疗性药物的可能性。方法以硫乙甘肽(Mercaptoacetyltriglycine,MAG3)作为双功能螯合剂,采用间接标记法,试验不同标记条件对标记率的影响。标记完成后检测生物活性、体外稳定性及正常小白鼠的体内分布。结果在最佳标记条件下,Morpholino的标记率为65%±12%,纯化后放化纯度>93%,比活度为(2.37±0.32)MBq/μg。稳定性检测发现,标记物在体外出现再氧化,导致188Re-Morpholino出现解离。加入抗氧化剂抗坏血酸(VitC)后可以显著提高体外稳定性。正常鼠生物分布显示,Morpholinos主要通过肾脏排泄,甲状腺及胃的摄取明显高于其他器官。结论以MAG3作螯合剂,188Re可以成功标记Morpholino寡核苷酸;188Re-Morpholino标记物体外稳定性较差,虽然加入抗氧化剂可以提高体外稳定性,但标记物在体内仍出现解离,因此,目前的标记方法可能不适合作为治疗药物。Objective To study the possibility of rhenium-188(188Re)-labeled morpholino oligonucleotide as a therapeutic drug.Methods Mercaptoacetyltriglycine(MAG3) was used as a bifunctional chelater to test the effect of 188Re-labelled morpholino oligonucleotide on labeling rate.Biological activity,in vitro stability and distribution of 188Re-labeled morpholino oligonucleotide in normal mice were detected.Results The labeling rate of 188Re-labeled morpholino oligonucleotide was 65%±12% with a radiochemical purity of over 93% and a specific activity of(2.37±0.32)MBq/μg.Re-oxidation of markers occurred in vitro,which caused disassociation of 188Re-labeled morpholino oligonucleotide.Addition of anti-oxidant and ascorbic acid into 188Re-labeled morpholino oligonucleotide could significantly improve its in vitro stability.188Re-labelled morpholino oligonucleotide was mainly excreted through the kidneys.Its uptake was significantly higher in thyroid and stomach.Conclusion MAG3 can label 188Re-labeled morpholino oligonucleotide with a poor in vitro stability.Addition of anti-oxidant into 188Re-labeled morpholino oligonucleotide can improve its in vitro stability,but the markers will disassociate in vivo.Thus,188Re-labeled morpholino oligonucleotide cannot be used as a therapeutic drug.
关 键 词:Morpholino寡核苷 铼-188 生物学标记
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