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巨噬细胞对镁合金体外腐蚀行为的影响。

Effect of macrophages on in vitro corrosion behavior of magnesium alloy.

作者信息

Zhang Jian, Hiromoto Sachiko, Yamazaki Tomohiko, Niu Jialin, Huang Hua, Jia Gaozhi, Li Haiyan, Ding Wenjiang, Yuan Guangyin

机构信息

National Engineering Research Center of Light Alloy Net Forming and State Key Laboratory of Metal Matrix Composite, School of Materials Science and Engineering, Shanghai Jiao Tong University, Shanghai, People's Republic of China.

Biomaterials Unit, International Center for Materials Nanoarchitectonics (WPI-MANA), National Institute for Materials Science, Tsukuba, Japan.

出版信息

J Biomed Mater Res A. 2016 Oct;104(10):2476-87. doi: 10.1002/jbm.a.35788. Epub 2016 Jun 6.

Abstract

The influence of cells on the corrosion behavior of biomedical magnesium alloy is an important but less studied topic, which is helpful for understanding the inconsistent corrosion rates between in vitro and in vivo experiments. In this work, macrophages were directly cultured on Mg-2.1Nd-0.2Zn-0.5Zr (wt %, abbreviated as JDBM) alloy surface for 72 or 168 hours. Macrophages retained good viability and the generation of reactive oxygen species (ROS) was greatly promoted on the alloy. Weight loss, Mg(2+) concentration, and cross-section observation results demonstrated that macrophages accelerated the in vitro corrosion of JDBM. The coverage of cell body did not affect the local thickness of corrosion product layer. The corrosion product layer had a porous inner Mg(OH)2 layer and a dense outer layer mainly composed of O, P, Mg, and Ca. The uniform acceleration of JDBM corrosion was attributed to the omnidirection diffusion of ROS from macrophages. © 2016 Wiley Periodicals, Inc. J Biomed Mater Res Part A: 104A: 2476-2487, 2016.

摘要

细胞对生物医用镁合金腐蚀行为的影响是一个重要但研究较少的课题,这有助于理解体外和体内实验中不一致的腐蚀速率。在本研究中,将巨噬细胞直接培养在Mg-2.1Nd-0.2Zn-0.5Zr(重量百分比,缩写为JDBM)合金表面72或168小时。巨噬细胞保持良好的活力,并且合金上活性氧(ROS)的生成大大增加。失重、Mg(2+)浓度和横截面观察结果表明,巨噬细胞加速了JDBM的体外腐蚀。细胞体的覆盖度不影响腐蚀产物层的局部厚度。腐蚀产物层有一个多孔的内层Mg(OH)2层和一个主要由O、P、Mg和Ca组成的致密外层。JDBM腐蚀的均匀加速归因于ROS从巨噬细胞的全方位扩散。© 2016威利期刊公司。《生物医学材料研究杂志》A部分:104A:2476 - 2487,2016年。

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