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Therapeutic efficacy of a polymeric micellar doxorubicin infused by convection-enhanced delivery against intracranial 9L brain tumor models

机译:对流增强输注注入的聚合物胶束阿霉素对颅内9L脑肿瘤模型的治疗功效

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摘要

Convection-enhanced delivery (CED) with various drug carrier systems has recently emerged as a novel chemotherapeutic method to overcome the problems of current chemotherapies against brain tumors. Polymeric micelle systems have exhibited dramatically higher in vivo antitumor activity in systemic administration. This study investigated the effectiveness of CED with polymeric micellar doxorubicin (DOX) in a 9L syngeneic rat model. Distribution, toxicity, and efficacy of free, liposomal, and micellar DOX infused by CED were evaluated. Micellar DOX achieved much wider distribution in brain tumor tissue and surrounding normal brain tissue than free DOX. Tissue toxicity increased at higher doses, but rats treated with micellar DOX showed no abnormal neurological symptoms at any dose tested (0.1–1.0 mg/ ml). Micellar DOX infused by CED resulted in prolonged median survival (36 days) compared with free DOX (19.6 days; p = 0.0173) and liposomal DOX (16.6 days; p = 0.0007) at the same dose (0.2 mg/ml). This study indicates the potential of CED with the polymeric micelle drug carrier system for the treatment of brain tumors.
机译:具有各种药物载体系统的对流增强递送(CED)最近已经成为一种新型的化学治疗方法,可以克服目前针对脑肿瘤的化学治疗方法的问题。高分子胶束系统在全身给药中表现出显着更高的体内抗肿瘤活性。这项研究调查了9L同系大鼠模型中CED与聚合物胶束阿霉素(DOX)的有效性。评估了通过CED注入的游离,脂质体和胶束DOX的分布,毒性和功效。胶束DOX比游离DOX在脑肿瘤组织和周围正常脑组织中的分布要广得多。高剂量时组织毒性增加,但用胶束DOX处理的大鼠在任何测试剂量(0.1–1.0 mg / ml)下均未显示异常神经系统症状。与相同剂量(0.2 mg / ml)的游离DOX(19.6天; p = 0.0173)和脂质体DOX(16.6天; p = 0.0007)相比,CED注入的胶束DOX可延长中位生存期(36天)。这项研究表明,具有聚合物胶束药物载体系统的CED在治疗脑肿瘤方面具有潜力。

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