Real-time in vivo detection of biomaterial-induced reactive oxygen species

被引:105
作者
Liu, Wendy E. [3 ,4 ]
Ma, Minglin [3 ,4 ]
Bratlie, Kaitlin M. [2 ,3 ,4 ]
Dang, Tram T. [2 ]
Langer, Robert [1 ,2 ,3 ,4 ]
Anderson, Daniel G. [1 ,2 ,3 ,4 ]
机构
[1] MIT, Div Hlth Sci & Technol, Cambridge, MA 02139 USA
[2] MIT, Dept Chem Engn, Cambridge, MA 02139 USA
[3] MIT, David H Koch Inst Integrat Canc Res, Cambridge, MA 02139 USA
[4] Childrens Hosp, Dept Anesthesiol, Boston, MA 02115 USA
基金
美国国家卫生研究院;
关键词
Biocompatibility; Immune response; Foreign body response; Free radical; HUMAN-NEUTROPHILS; PROTEASE ACTIVITY; OXIDATIVE STRESS; MECHANISMS; OXIDASE; INFLAMMATION; SUPEROXIDE; ACTIVATION; RESPONSES; CANCER;
D O I
10.1016/j.biomaterials.2010.11.029
中图分类号
R318 [生物医学工程];
学科分类号
0831 ;
摘要
The non-specific host response to implanted biomaterials is often a key challenge of medical device design. To evaluate biocompatibility, measuring the release of reactive oxygen species (ROS) produced by inflammatory cells in response to biomaterial surfaces is a well-established method. However, the detection of ROS in response to materials implanted in vivo has not yet been demonstrated. Here, we develop a bioluminescence whole animal imaging approach to observe ROS released in response to subcutaneously-implanted materials in live animals. We compared the real-time generation of ROS in response to two representative materials, polystyrene and alginate, over the course of 28 days. High levels of ROS were observed near polystyrene, but not alginate implants, and persisted throughout the course of 28 days. Histological analysis revealed that high levels of ROS correlated not only with the presence of phagocytic cells at early timepoints, but also fibrosis at later timepoints, suggesting that ROS may be involved in both the acute and chronic phase of the foreign body response. These data are the first in vivo demonstration of ROS generation in response to implanted materials, and describe a novel technique to evaluate the host response. (C) 2010 Elsevier Ltd. All rights reserved.
引用
收藏
页码:1796 / 1801
页数:6
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