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Galactosylated Chitosan Oligosaccharide Nanoparticles for Hepatocellular Carcinoma Cell-Targeted Delivery of Adenosine Triphosphate

机译:半乳糖基化的壳聚糖寡糖纳米颗粒用于肝细胞癌细胞靶向递送三磷酸腺苷。

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Nanoparticles composed of galactosylated chitosan oligosaccharide (Gal-CSO) and adenosine triphosphate (ATP) were prepared for hepatocellular carcinoma cell-specific uptake, and the characteristics of Gal-CSO/ATP nanoparticles were evaluated. CSO/ATP nanoparticles were prepared as a control. The average diameter and zeta potential of Gal-CSO/ATP nanoparticles were 51.03 ± 3.26 nm and 30.50 ± 1.25 mV, respectively, suggesting suitable properties for a drug delivery system. Subsequently, the cytotoxicity of Gal-CSO/ATP nanoparticles were examined by the methyl tetrazolium (MTT) assay, and the half maximal inhibitory concentration (IC50) values were calculated with HepG2 (human hepatocellular carcinoma cell line) cells. The results showed that the cytotoxic effect of nanoparticles on HepG2 cells was low. In the meantime, it was also found that the Gal-CSO/ATP nanoparticles could be uptaken by HepG2 cells, due to expression of the asialoglycoprotein receptor (ASGP-R) on their surfaces. The presented results indicate that the Gal-CSO nanoparticles might be very attractive to be used as an intracellular drug delivery carrier for hepatocellular carcinoma cell targeting, thus warranting further in vivo or clinical investigations.
机译:制备了由半乳糖基化壳聚糖寡糖(Gal-CSO)和三磷酸腺苷(ATP)组成的纳米颗粒,用于肝癌细胞特异性摄取,并评估了Gal-CSO / ATP纳米颗粒的特性。制备CSO / ATP纳米颗粒作为对照。 Gal-CSO / ATP纳米粒子的平均直径和Zeta电位分别为51.03±3.26 nm和30.50±1.25 mV,这表明该系统适合用于药物输送系统。随后,通过甲基四氮唑(MTT)检测法检测Gal-CSO / ATP纳米颗粒的细胞毒性,并用HepG2(人肝癌细胞系)计算半数最大抑制浓度(IC 50 )值) 细胞。结果显示纳米颗粒对HepG2细胞的细胞毒性作用低。同时,还发现,由于去唾液酸糖蛋白受体(ASGP-R)在其表面表达,Gal-CSO / ATP纳米颗粒可被HepG2细胞摄取。提出的结果表明,Gal-CSO纳米颗粒用作肝细胞癌细胞靶向的细胞内药物传递载体可能非常有吸引力,因此有必要进行进一步的体内或临床研究。

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