90y标记卟啉- dota缀合物的合成及生物学评价:一种潜在的靶向肿瘤治疗分子。

Cancer biotherapy & radiopharmaceuticals Pub Date : 2013-11-01 Epub Date: 2013-07-09 DOI:10.1089/cbr.2013.1512
Sweety Mittal, Mohini Bhadwal, Tapas Das, Haladhar Dev Sarma, Rubel Chakravarty, Ashutosh Dash, Sharmila Banerjee, M R A Pillai
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引用次数: 14

摘要

合成了不对称取代卟啉5-[4-(3-氨基)-n-丙氧基苯基]-10,15,20-三-(4-羧基亚甲基氧基苯基)卟啉,并与对- ncs -苄基- dota[对异硫氰酸酯-苄基-1,4,7,10-四氮杂环十二烷-1,4,7,10-四乙酸]偶联,探索其在肿瘤靶向治疗中的潜力。卟啉- dota偶联物用国产90Sr/90Y电化学发生器获得的90Y进行放射性标记。在携带纤维肉瘤肿瘤的瑞士小鼠中进行的生物分布研究显示,在注射后30分钟内,肿瘤摄取良好(每g肿瘤注射活性约3.4%)。肿瘤活性随着时间的推移而下降,然而,由于非靶器官最初积累的活性被清除,肿瘤与血液和肿瘤与肌肉的比例在给药后4天显著增加。非积累活性主要通过肾脏途径清除。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Synthesis and biological evaluation of 90Y-labeled porphyrin-DOTA conjugate: a potential molecule for targeted tumor therapy.

An unsymmetrically substituted porphyrin, 5-[4-(3-amino)-n-propyloxyphenyl]-10,15,20-tris-(4-carboxymethyleneoxyphenyl)porphyrin, was synthesized and coupled with p-NCS-benzyl-DOTA [p-isothiocyanato-benzyl-1,4,7,10-tetraazacyclododecane-1,4,7,10-tetraacetic acid] for exploring its possible potential in targeted tumor therapy. The porphyrin-DOTA conjugate was radiolabeled with 90Y, obtained from a 90Sr/90Y electrochemical generator, developed in-house. Biodistribution studies performed in Swiss mice bearing fibrosarcoma tumor showed good tumor uptake (∼3.4% injected activity in per g of tumor) within 30 minutes postinjection. The tumor activity decreased with the progress of time, however, tumor to blood and tumor to muscle ratios considerably increased at 4 days postadministration owing to the clearance of the initially accumulated activities from the nontarget organs. The nonaccumulated activity exhibited major clearance through renal pathway.

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