...
首页> 外文期刊>Cellular oncology >Drug-targeting in combined cancer chemotherapy: tumor growth inhibition in mice by association of paclitaxel and etoposide with a cholesterol-rich nanoemulsion.
【24h】

Drug-targeting in combined cancer chemotherapy: tumor growth inhibition in mice by association of paclitaxel and etoposide with a cholesterol-rich nanoemulsion.

机译:联合癌症化疗中的药物靶向:紫杉醇和依托泊苷与富含胆固醇的纳米乳剂的结合可抑制小鼠的肿瘤生长。

获取原文
获取原文并翻译 | 示例
   

获取外文期刊封面封底 >>

       

摘要

Lipid nanoemulsions (LDE) may be used as carriers of paclitaxel (PTX) and etoposide (ETP) to decrease toxicity and increase the therapeutic action of those drugs. The current study investigates the combined chemotherapy with PTX and ETP associated with LDE.Four groups of 10-20 B16F10 melanoma-bearing mice were treated with LDE-PTX and LDE-ETP in combination (LDE-PTX?+?ETP), commercial PTX and ETP in combination (PTX?+?ETP), single LDE-PTX, and single LDE-ETP. PTX and ETX doses were 9?μmol/kg administered in three intraperitoneal injections on three alternate days. In two control groups mice were treated with saline solution or LDE alone. Tumor growth, metastasis presence, cell-cycle distribution, blood cell counts and histological data were analyzed. Toxicity of all treatments was evaluated in mice without tumors.Tumor growth inhibition was similarly strong in all treatment groups. However, there was a greater reduction in the number of animals bearing metastases in the LDE-PTX?+?ETP group (30?%) in comparison to the PTX?+?ETP group (82?%, p?
机译:脂质纳米乳剂(LDE)可用作紫杉醇(PTX)和依托泊苷(ETP)的载体,以降低毒性并增强这些药物的治疗作用。目前的研究是对PTX和ETP联合LDE联合化疗的研究.10组20-20只B16F10黑色素瘤小鼠接受LDE-PTX和LDE-ETP联合治疗(LDE-PTX?+?ETP),商业PTX和ETP组合(PTX→+ ETP),单个LDE-PTX和单个LDE-ETP。 PTX和ETX剂量为9?μmol/ kg,每隔3天进行3次腹膜内注射。在两个对照组中,仅用盐溶液或LDE治疗小鼠。分析了肿瘤生长,转移的存在,细胞周期分布,血细胞计数和组织学数据。在没有肿瘤的小鼠中评估了所有治疗的毒性。在所有治疗组中,肿瘤生长抑制作用均相似。但是,与PTXα+βETP组相比,LDE-PTXα+βETP组中有转移的动物数量减少了(30%)(82%,p≤<0.05)。 。 LDE-PTXα+ΔETP组观察到肿瘤组织中细胞密度降低,血管减少和胶原蛋白纤维增加,而PTXα+ΔETP组则没有观察到,两组均降低了与黑素瘤相关的贫血和血小板减少观测到的。流式细胞仪分析表明,LDE-PTXα+ΔETP对肿瘤细胞的选择性高于PTX-ETP,在细胞周期的G(2)/ M期表现出停滞(65 %%)(p 0.001)。 。 LDE-PTX?+?ETP组的体重减轻和骨髓抑制表现出的毒性明显低于PTX?+?ETP组.LDE-PTX?+?ETP联合药物靶向治疗显示出显着的抗癌特性并降低了与PTX ++ ETP相比毒性小。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号