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L-赖氨酸修饰的 FeO 纳米颗粒用于磁性细胞标记。

L-Lysine-modified FeO nanoparticles for magnetic cell labeling.

机构信息

Postovsky Institute of Organic Synthesis, Russian Academy of Sciences (Ural Branch), 22 S. Kovalevskoy St., Yekaterinburg, 620990, Russia.

Postovsky Institute of Organic Synthesis, Russian Academy of Sciences (Ural Branch), 22 S. Kovalevskoy St., Yekaterinburg, 620990, Russia.

出版信息

Colloids Surf B Biointerfaces. 2020 Jun;190:110879. doi: 10.1016/j.colsurfb.2020.110879. Epub 2020 Feb 19.

Abstract

The efficiency of magnetic labeling with L-Lys-modified FeO magnetic nanoparticles (MNPs) and the stability of magnetization of rat adipose-derived mesenchymal stem cells, lineage-negative (Lin(-)) hematopoietic progenitor cells from mouse bone marrow and human leukemia K562 cells were studied. For this purpose, covalent modification of MNPs with 3-aminopropylsilane and N-di-Fmoc-L-lysine followed by removal of N-protecting groups was carried out. Since the degree of hydroxylation of the surface of the starting nanoparticles plays a crucial role in the silanization reaction and the possibility of obtaining stable colloidal solutions. In present work we for the first time performed a comparative qualitative and quantitative evaluation of the number of adsorbed water molecules and hydroxyl groups on the surface of chemically and physically obtained FeO MNPs using comprehensive FTIR spectroscopy and thermogravimetric analysis. The results obtained can be further used for magnetic labeling of cells in experiments in vitro and in vivo.

摘要

本研究旨在考察 L-赖氨酸修饰的 FeO 磁性纳米颗粒(MNPs)的磁标记效率,以及鼠骨髓来源的间充质干细胞、Lin(-)造血祖细胞和人白血病 K562 细胞的磁化稳定性。为此,采用 3-氨丙基硅烷和 N-二芴甲氧羰基-L-赖氨酸对 MNPs 进行共价修饰,然后去除 N-保护基团。由于起始纳米颗粒表面的羟基化程度在硅烷化反应中起着至关重要的作用,并且影响到能否获得稳定的胶体溶液。在本工作中,我们首次使用全面的傅里叶变换红外光谱和热重分析,对化学法和物理法制备的 FeO MNPs 表面吸附的水分子和羟基的数量进行了定性和定量比较评价。所得结果可进一步用于细胞的体外和体内磁标记实验。

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