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通过脑靶向系统共递送阿霉素和小干扰RNA用于胶质瘤治疗:血管活性肠肽-2修饰的聚乳酸-羟基乙酸共聚物纳米粒

Co-delivery of doxorubicin and siRNA for glioma therapy by a brain targeting system: angiopep-2-modified poly(lactic-co-glycolic acid) nanoparticles.

作者信息

Wang Lei, Hao Yongwei, Li Haixia, Zhao Yalin, Meng Dehui, Li Dong, Shi Jinjin, Zhang Hongling, Zhang Zhenzhong, Zhang Yun

机构信息

a School of Pharmaceutical Sciences, Zhengzhou University , Zhengzhou , PR China.

出版信息

J Drug Target. 2015;23(9):832-46. doi: 10.3109/1061186X.2015.1025077. Epub 2015 Apr 9.

Abstract

It is very challenging to treat brain cancer because of the blood-brain barrier (BBB) restricting therapeutic drug or gene to access the brain. In this research project, angiopep-2 (ANG) was used as a brain-targeted peptide for preparing multifunctional ANG-modified poly(lactic-co-glycolic acid) (PLGA) nanoparticles (NPs), which encapsulated both doxorubicin (DOX) and epidermal growth factor receptor (EGFR) siRNA, designated as ANG/PLGA/DOX/siRNA. This system could efficiently deliver DOX and siRNA into U87MG cells leading to significant cell inhibition, apoptosis and EGFR silencing in vitro. It demonstrated that this drug system was capable of penetrating the BBB in vivo, resulting in more drugs accumulation in the brain. The animal study using the brain orthotopic U87MG glioma xenograft model indicated that the ANG-targeted co-delivery of DOX and EGFR siRNA resulted in not only the prolongation of the life span of the glioma-bearing mice but also an obvious cell apoptosis in glioma tissue.

摘要

由于血脑屏障(BBB)限制治疗药物或基因进入大脑,治疗脑癌极具挑战性。在本研究项目中,血管活性肠肽-2(ANG)被用作脑靶向肽,用于制备多功能ANG修饰的聚乳酸-羟基乙酸共聚物(PLGA)纳米颗粒(NPs),其同时包裹了阿霉素(DOX)和表皮生长因子受体(EGFR)小干扰RNA(siRNA),命名为ANG/PLGA/DOX/siRNA。该系统能够有效地将DOX和siRNA递送至U87MG细胞,在体外导致显著的细胞抑制、凋亡和EGFR沉默。结果表明,该药物系统能够在体内穿透血脑屏障,使更多药物在脑内蓄积。使用脑原位U87MG胶质瘤异种移植模型的动物研究表明,ANG靶向共递送DOX和EGFR siRNA不仅延长了荷瘤小鼠的寿命,而且在胶质瘤组织中引起明显的细胞凋亡。

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