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Preparation of pectin-based nanosized drug delivery system with diverse morphologies and their targeting antitumor effect on hepatocellular carcinoma cells

机译:具有不同形态的果胶基纳米型药物递送系统的制备及其对肝细胞癌细胞的靶向抗肿瘤作用

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This study was aim to find out the best morphology that have the best targeting on hepatocellular carcinoma cells. The drug-loaded pectin nanospheres, vesicles and nanorods were fabricated in aqueous media containing Ca~(2+) and CO_3~(2-) ions. Through adjusting the preparation conditions, nanosized drug delivery system with diverse morphologies, that is, nanospheres, vesicles and nanorod could be obtained. The cell survival rate were determined by Trypan blue staining method. CCK-8 method was used to study the inhibition effect of 5-FU, drug-loaded pectin. Nanospheres, vesicles and nanorods and blank drug loaded systerm on HepG2 cell line. Cellular uptakes were determined by HPLC method. DNA fragments by agarose gel electrophoresis, flow cytometry and Hoechst staining were used to confirm the death of the HepG2 cell. The nanospheres have the best targeting and antitumor effect on hepatocellular carcinoma cells.
机译:本研究旨在探讨肝细胞癌细胞最佳靶向的最佳形态。在含有Ca〜(2+)和CO_3〜(2-)离子的水性介质中制造了药物果胶蛋白纳米球,囊泡和纳米棒。通过调节制备条件,可以获得具有多种形态的纳米药物输送系统,即纳米球,囊泡和纳米棒。细胞存活率由台盼蓝染色方法确定。 CCK-8方法用于研究5-FU,载药果胶的抑制作用。纳米球,囊泡和纳米棒和含有HOPG2细胞系上的空白药物的Systerm。通过HPLC方法测定细胞上升。通过琼脂糖凝胶电泳,流式细胞术和Hoechst染色的DNA片段用于确认HepG2细胞的死亡。纳米球对肝细胞癌细胞具有最佳的靶向和抗肿瘤作用。

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