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Host-Guest Interaction Mediated Assembilies: Supramolecular Nanoparticles for Paclitaxel/siRNA Co-delivery

机译:宿主—来宾相互作用介导的大会:紫杉醇/ siRNA共交付的超分子纳米粒子。

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摘要

To achieve synergistic effect of anti-tumor agent and therapeutic gene, a novel type supramolecular nanoparticle which perform co-delivery of paclitaxel and siRNA was synthesized via host-guest interaction. In the self-assembly complex (termed as PC/Ada-PTX), the cationic PEI_(600)-CD (PC) vectors composed of β -cyclodextrin (β-CD) and low-molecular-weight polyethylenimine (PEI, Mw 600) served as the host and the adamantane-conjugated paclitaxel (Ada-PTX) as the guest. The cytotoxicity of the PC/Ada-PTX complex was much lower than that of PEI 25 kD in SKOV-3 cell line. Functioning of paclitaxel accompanied by siRNA which silenced the survivin gene exhibited novel lethality to the tumor cells, which is confirmed by significant up-regulation of cell-cycle arrest and cell apoptosis. By hypodermic injection of the SNP into the tumor-bearing nude mice, it was found that the SNP remarkably enhanced the anti-tumor effect. The host-guest assembled SNP should have great potential applications in cancer therapy.
机译:为了实现抗肿瘤剂和治疗基因的协同作用,通过宿主-客体相互作用合成了新型的紫杉醇和siRNA共同递送的超分子纳米颗粒。在自组装复合物(称为PC / Ada-PTX)中,由β-环糊精(β-CD)和低分子量聚乙烯亚胺(PEI,Mw 600)组成的阳离子PEI_(600)-CD(PC)载体)做为宿主,金刚烷共轭紫杉醇(Ada-PTX)做为客人。在SKOV-3细胞系中,PC / Ada-PTX复合物的细胞毒性远低于PEI 25 kD。紫杉醇伴随沉默沉默survivin基因的siRNA的功能对肿瘤细胞表现出新的致死性,这可以通过细胞周期停滞和细胞凋亡的显着上调来证实。通过将SNP皮下注射到荷瘤裸鼠中,发现SNP显着增强了抗肿瘤作用。来宾组装的SNP在癌症治疗中应具有巨大的潜在应用。

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