Department of Biology, Chemistry, and Pharmacy, Freie Universität Berlin, Takustrasse 3, 14195 Berlin, Germany.
Small. 2011 Mar 21;7(6):820-9. doi: 10.1002/smll.201002220. Epub 2011 Feb 18.
To study the mechanism of cellular internalization, hyperbranched polyether derivatives consisting of amino-bearing hyperbranched polyglycerols (HPGs) of varied molecular mass and size range are designed and synthesized. HPGs were further fluorescently labelled by conjugating maleimido indocarbocyanine dye (ICC-mal). The conjugates are characterized by UV-vis spectroscopy, fluorescence profile, zeta potential, and dynamic light scattering. The uptake mechanism is studied by fluorescence-activated cell sorting (FACS) analysis, fluorescence spectroscopy, and confocal microscopy with human lung cancer cells A549, human epidermoid carcinoma cells A431, and human umbilical vein endothelial cells (HUVEC) cells. For the first time, the results suggest that the higher-molecular-weight HPGs (40-870 kDa) predominantly accumulate in the cytoplasm much better than their low-molecular-weight counterparts (2-20 kDa). The HPG nanocarriers discussed here have many biomedical implications, particularly for delivering drugs to the targeted site.
为了研究细胞内化的机制,设计并合成了由不同分子量和尺寸范围的带有氨基的超支化聚甘油(HPG)组成的超支化聚醚衍生物。HPG 进一步通过连接马来酰亚胺吲哚碳菁染料(ICC-mal)进行荧光标记。通过紫外可见光谱、荧光谱、Zeta 电位和动态光散射对这些偶联物进行了表征。通过荧光激活细胞分选(FACS)分析、荧光光谱和共聚焦显微镜,用人肺癌细胞 A549、人表皮癌细胞 A431 和人脐静脉内皮细胞(HUVEC)细胞研究了摄取机制。结果首次表明,高分子量 HPG(40-870 kDa)比低分子量 HPG(2-20 kDa)更优先地在细胞质中积累。这里讨论的 HPG 纳米载体具有许多生物医学意义,特别是在将药物递送到靶向部位方面。