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Synthesis of immunomagnetic nanoparticles and their application in the separation and purification of CD34(+) hematopoietic stem cells

机译:免疫磁性纳米粒子的合成及其在CD34(+)造血干细胞分离纯化中的应用

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摘要

The silica-coated superparamagnetic nanoparticles with the uniform diameter of about 60 nm were synthesized-by reverse microemulsions method. And the magnetic nanoparticles were modified with N-(2-aminoethyl)-3-aminopropyltrimethoxysilane (AEAPS). The immunomagnetic nanoparticles were then successfully prepared by covalently immobilizing anti-CD34(+) monoclonal antibodies to the surface of amino silane modified magnetic particles. The cell separation results showed that the synthesized immunomagnetic nanoparticles could rapidly and conveniently separate the CD34(+) cells with high efficiency and specificity than normal ones. The surface morphology of separated target cells was examined by scanning electron microscope (SEM). Atomic force microscope (AFM) also characterized the magnetic materials on the surface of the separated target cells for the first time, which further confirmed that the target cells were separated by the immunomagnetic nanoparticles. The viability of the separated cells was studied by culturing method and Beckman Vi-cell viability analyst. Therefore, our experiments provided a new, direct, rapid mode to separate target cells. (c) 2006 Elsevier B.V. All rights reserved.
机译:采用反向微乳液法合成了直径约60nm的二氧化硅包覆的超顺磁性纳米粒子。并用N-(2-氨基乙基)-3-氨基丙基三甲氧基硅烷(AEAPS)修饰了磁性纳米粒子。然后通过将抗CD34(+)单克隆抗体共价固定在氨基硅烷修饰的磁性颗粒表面上,成功制备了免疫磁性纳米颗粒。细胞分离结果表明,所合成的免疫磁性纳米颗粒与常规细胞相比,可以快速,方便地分离CD34(+)细胞,具有较高的效率和特异性。通过扫描电子显微镜(SEM)检查分离的靶细胞的表面形态。原子力显微镜(AFM)还首次对分离的靶细胞表面上的磁性材料进行了表征,这进一步证实了靶细胞已被免疫磁性纳米颗粒分离。通过培养方法和贝克曼Vi-细胞活力分析仪研究分离的细胞的活力。因此,我们的实验提供了一种新的,直接的,快速的模式来分离靶细胞。 (c)2006 Elsevier B.V.保留所有权利。

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