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首页> 外文期刊>Artificial cells, nanomedicine, and biotechnology. >The study of establishment of an in vivo tumor model by three-dimensional cells culture systems methods and evaluation of antitumor effect of biotin-conjugated pullulan acetate nanoparticles
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The study of establishment of an in vivo tumor model by three-dimensional cells culture systems methods and evaluation of antitumor effect of biotin-conjugated pullulan acetate nanoparticles

机译:三维细胞培养系统方法建立体内肿瘤模型的研究及生物素共轭乙酸支链淀粉纳米粒子的抗肿瘤作用评估

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摘要

In this study, three-dimensional (3D) hydrogels were used for human hepatocellular carcinoma (HepG2) cells culture systems in vitro and establishment of an in vivo xenografted tumor model. Based on our previous work on the biotin-conjugated pullulan acetate nanoparticles (Bio-PA NPs) as anticancer drug carriers, we further studied the anti-tumor effect of the NPs in two-dimensional (2D) and 3D cell culture system. When embedded in 3D hydrogels, HepG2 cells formed tumor spheroids and the cytoplasmic actin microfilamentrates were rearranged over a period of 7?days. In vitro cytotoxicity results indicated that HepG2 cells in 3D hydrogels were more resistant to Bio-PA NPs treatments compared to the 2D system. The tumor formation rate of in vivo xenografted tumor model using 3D culture systems method was 98.2%, which was significantly higher than that using of 2D cultured cells (76.4%). Then we injected the 3D HepG2 cells systems in the right anterior axillary of female Balb/c nude mice, and evaluate the in vivo anti-tumor efficacy of Bio-PA NPs. In summary, these results suggested that HepG2 cells in 3D hydrogel system has shown the potential to provide an in vitro and in vivo model and for the evaluation of Bio-PA NPs. Graphical Abstract Schematic illustration for the preparation of Bio-PA/EPI NPs using dialysis method and establishment of tumor model in vivo and in vitro . Schematic illustration for the preparation of Bio-PA/EPI NPs using dialysis method and establishment of tumor model in vivo and in vitro .
机译:在这项研究中,三维(3D)水凝胶用于人类肝细胞癌(HepG2)细胞体外培养系统和体内异种移植肿瘤模型的建立。基于我们先前关于生物素缀合的醋酸支链淀粉纳米颗粒(Bio-PA NPs)作为抗癌药物载体的工作,我们进一步研究了NPs在二维(2D)和3D细胞培养系统中的抗肿瘤作用。当嵌入3D水凝胶中时,HepG2细胞形成肿瘤球体,并且细胞质肌动蛋白微丝率在7天的时间内重新排列。体外细胞毒性结果表明,与2D系统相比,3D水凝胶中的HepG2细胞对Bio-PA NPs处理更具抵抗力。使用3D培养系统方法的体内异种移植肿瘤模型的肿瘤形成率为98.2%,显着高于使用2D培养细胞的肿瘤形成率为76.4%。然后,我们将3D HepG2细胞系统注入雌性Balb / c裸鼠的右前腋窝,并评估Bio-PA NP的体内抗肿瘤功效。总之,这些结果表明3D水凝胶系统中的HepG2细胞已显示出提供体外和体内模型以及评估Bio-PA NP的潜力。用透析方法制备Bio-PA / EPI NP的图解示意图和体内外肿瘤模型的建立。用透析法制备Bio-PA / EPI NP的示意图并建立体内外肿瘤模型。

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