125I-Iododeoxyuridine for the Treatment of a Brain Tumor Model:Selection of Conditions for Optimal Effectiveness

S. Lehnert, Yongbiao Li, E. Bump, Bill Riddoch, A. Chenite, M. Shive
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引用次数: 2

Abstract

The intent of this study was to optimise conditions for the use of 125 IUdR in the treatment of cancer. The radiopharmaceutical plus a biomodulator, methotrexate (MTX) was delivered by intra-tumoral injection of a thermosensitive hydrogel forming a slow release depot of 125 IUdR and MTX in the tumor. Methods: The C6 rat glioblastoma was implanted intra-cranially. A chitosan polymer was used to formulate a biodegradable and biocompatible implant for controlled intra-tumoral delivery of 125 IUdR plus MTX. Results: Intratumoral implant of hydrogel loaded with 7.0 -7.4 MBq of 125 IUdR resulted in survival of 20% of treated animals to 180 days after tumor implant. Simultaneous delivery of MTX increased the number of rats that were effectively cured, to 40%. Conclusion: Using an injectable thermolabile hydrogel as vehicle for 125 IUdR delivery a higher level of tumor control was achieved in a rat glioma model than had been previously reported.
125i -碘脱氧尿苷治疗脑肿瘤模型:最佳疗效条件的选择
本研究的目的是优化125 IUdR用于癌症治疗的条件。这种放射性药物加上生物调节剂甲氨蝶呤(MTX)是通过在肿瘤内注射热敏水凝胶来传递的,在肿瘤中形成125 IUdR和MTX的缓释库。方法:颅内植入C6大鼠胶质母细胞瘤。采用壳聚糖聚合物制备可生物降解和生物相容性的植入物,用于控制125 IUdR加MTX的肿瘤内输送。结果:载7.0 -7.4 MBq的125 IUdR的水凝胶植入瘤内,20%的治疗动物存活至肿瘤植入后180天。同时给予甲氨蝶呤使有效治愈的大鼠数量增加到40%。结论:使用可注射的可热性水凝胶作为125 IUdR的载体,在大鼠胶质瘤模型中实现了比以前报道的更高水平的肿瘤控制。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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