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首页> 外文期刊>International Journal of Pharmaceutics >Cell-polymer interactions of fluorescent polystyrene latex particles coated with thermosensitive poly(N-isopropylacrylamide) and poly(N-vinylcaprolactam) or grafted with poly(ethylene oxide)-macromonomer.
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Cell-polymer interactions of fluorescent polystyrene latex particles coated with thermosensitive poly(N-isopropylacrylamide) and poly(N-vinylcaprolactam) or grafted with poly(ethylene oxide)-macromonomer.

机译:涂有热敏性聚(N-异丙基丙烯酰胺)和聚(N-乙烯基己内酰胺)或接枝有聚(环氧乙烷)-大分子单体的荧光聚苯乙烯胶乳颗粒的细胞-聚合物相互作用。

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摘要

Cell-polymer interactions of thermosensitive poly(N-isopropylacrylamide) (PNIPAM) or poly(N-vinylcaprolactam) (PVCL) coated particles with RAW264.7 macrophages and intestinal Caco-2 cells were evaluated. Nanosized particles were prepared by modifying the surface of fluorescent polystyrene (FPS) particles with the thermosensitive polymer gels or with poly(ethylene oxide) (PEO)-macromonomer grafts. The particles were characterized by IR-spectroscopy for functional groups, light scattering for size distribution and zeta-potential for surface charge. Effects of temperature and polymer coating/grafting on the cellular interactions were evaluated by cell association/uptake and visualized by confocal scanning microscope. PEO and PNIPAM inhibited the polymer-cell contact by steric repulsion, evidenced by weak attachment of the particles. PVCL-coated FPS was adsorbed on the cells more strongly, especially at 37 degrees C, because of more hydrophobic nature at higher temperatures. The results suggest feasibilityof the PNIPAM and PVCL for biotechnological/pharmaceutical applications, as the cell-particle interactions may be modified by size, surface charge, hydrophobicity, steric repulsion and temperature.
机译:评估了热敏性聚(N-异丙基丙烯酰胺)(PNIPAM)或聚(N-乙烯基己内酰胺)(PVCL)涂层颗粒与RAW264.7巨噬细胞和肠道Caco-2细胞的细胞-聚合物相互作用。通过用热敏聚合物凝胶或聚环氧乙烷(PEO)-大分子单体接枝改性荧光聚苯乙烯(FPS)颗粒的表面来制备纳米尺寸的颗粒。通过红外光谱对官能团,光散射进行粒度分布和ζ电势对表面电荷进行表征。通过细胞缔合/摄取评估温度和聚合物包被/接枝对细胞相互作用的影响,并通过共聚焦扫描显微镜可视化。 PEO和PNIPAM通过空间排斥抑制了聚合物-细胞的接触,这表现为颗粒的附着力弱。由于较高温度下的疏水性,PVCL涂层的FPS更牢固地吸附在细胞上,尤其是在37摄氏度时。结果表明PNIPAM和PVCL在生物技术/药物应用中的可行性,因为细胞-颗粒之间的相互作用可能会因大小,表面电荷,疏水性,空间排斥性和温度而改变。

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