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首页> 外文期刊>International Journal of Pharmaceutics >Therapeutic efficacy study of novel 5-FU-loaded PMM 2.1.2-based microspheres on C6 glioma.
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Therapeutic efficacy study of novel 5-FU-loaded PMM 2.1.2-based microspheres on C6 glioma.

机译:新型基于5-FU的PMM 2.1.2微球对C6神经胶质瘤的治疗功效研究。

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摘要

The aim of this study was to evaluate the potential of poly(methylidene malonate 2.1.2) as a new drug delivery system to the central nervous system. 5-Fluorouracil microspheres were formulated by an emulsion-extraction method, and evaluated on a C6 glioma model. Twenty-seven Sprague-Dawley female rats underwent implantation of various C6 cell concentrations. Magnetic resonance imaging was performed at day 10 to control the setting of the tumor, by using a T2-weighted sequence. At day 12, 18 animals received blank or 5-FU-loaded microspheres, while 9 animals were not implanted and constituted the controls. Thereafter, MRI was performed twice a week to follow the tumor growth. In 12 animals, an alloimmune rejection of the tumor was observed, showing the limitations of the C6 glioma model. When tumor developed, no relationship was observed between the number of C6 cells injected and the tumor volume. 5-FU microsphere efficacy could statistically be demonstrated by significantly improving the median survival of C6 glioma-bearing animals and also by decreasing tumor burden.
机译:这项研究的目的是评估聚(亚甲基丙二酸酯2.1.2)作为向中枢神经系统输送新药物的潜力。通过乳液萃取法配制5-氟尿嘧啶微球,并在C6神经胶质瘤模型上评估。二十七只Sprague-Dawley雌性大鼠接受了各种C6细胞浓度的植入。通过使用T2加权序列在第10天进行磁共振成像以控制肿瘤的形成。在第12天,有18只动物接受空白或5-FU负载的微球,而没有植入9只动物并构成对照。此后,每周两次进行MRI,以追踪肿瘤的生长。在12只动物中,观察到肿瘤的同种免疫排斥,显示出C6神经胶质瘤模型的局限性。当肿瘤发展时,注射的C6细胞数量与肿瘤体积之间没有关系。可以通过显着提高C6胶质瘤动物的中位存活率并降低肿瘤负担来从统计学上证明5-FU微球功效。

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