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首页> 外文期刊>Colloids and Surfaces, B. Biointerfaces >Fabrication of rigid and macroporous agarose microspheres by pre-cross-linking and surfactant micelles swelling method
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Fabrication of rigid and macroporous agarose microspheres by pre-cross-linking and surfactant micelles swelling method

机译:通过预交联和表面活性剂胶束制备刚性和大孔琼脂糖微球的溶胀法

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摘要

A novel combined method of pre-cross-linking and surfactant micelles swelling was proposed in this study to fabricate highly cross-linked and macroporous agarose (HMA) microspheres. Agarose was chemically modified by allylglycidyl ether (AGE) as heterobifunctional cross-linker via its active glycidyl moieties before gel formation and pre-cross-linking was achieved. By this means, the effective concentration of cross-linker presented in agarose gel increased significantly, and thus cross-linking with a high-efficiency was achieved. Further to enhance the intraparticle mass transfer of agarose microspheres, the surfactant micelles swelling method was utilized to create interconnected macropores. Under the optimal condition, HMA microspheres with homogeneous reticular structure and pore size of hundreds nanometers were successfully prepared. They exhibited a low backpressure with a flow velocity as high as 1987 cm/h, which was much higher than that of commercial Sepharose 4 F F. HMA microspheres were then derivatized with carboxymethyl (CM) groups and applied in ion-exchange chromatography. As expected, CM-HMA column separated model proteins effectively even at a flow velocity three times higher than that of commercial CM-4 F F. Visualization of dynamic protein adsorption by confocal laser scanning microscope (CLSM) revealed that the intraparticle mass transfer of CM-HMA micro spheres was intensified due to its macroporous structure. All of the results indicated the newly developed agarose microspheres were a promising medium for high-speed chromatography.
机译:在该研究中提出了一种新的结合方法的预交联和表面活性剂胶束溶胀,以制造高度交联和大孔琼脂糖(HMA)微球。通过其活性缩水甘油醚通过其活性缩水甘油基部分通过其活性缩水甘油基部分在凝胶形成和结交联之前,通过烯丙基乙基醚(年龄)化学改性。通过这种方式,在琼脂糖凝胶中呈现的交联剂的有效浓度显着增加,因此实现了与高效率的交联。此外,为了增强琼脂糖微球的椎间内部传质,使用表面活性剂胶束溶胀法来产生相互连接的大孔。在最佳状态下,成功制备了具有均匀网状结构和孔径的HMA微球。它们具有高达1987cm / h的流速表现出低的背压,其远高于商业琼脂糖4ff.HMA微球,然后用羧甲基(cm)基团衍生化并在离子交换色谱中施用。如预期的那样,CM-HMA柱分离的蛋白质甚至在比商业CM-4 F F高的流速下有效地有效。通过共聚焦激光扫描显微镜(CLSM)可视化动态蛋白质吸附的可视化,揭示了CM的粒前的传质-HMA微型球体由于其大孔结构而加强。所有结果表明,新开发的琼脂糖微球是高速色谱的有希望的介质。

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