Rapid Biocompatibility Analysis of Materials via In Vivo Fluorescence Imaging of Mouse Models

被引:50
作者
Bratlie, Kaitlin M. [1 ,2 ]
Dang, Tram T. [1 ,2 ]
Lyle, Stephen [3 ]
Nahrendorf, Matthias [4 ]
Weissleder, Ralph [4 ]
Langer, Robert [1 ,2 ,5 ]
Anderson, Daniel G. [2 ,5 ]
机构
[1] MIT, Dept Chem Engn, Cambridge, MA 02139 USA
[2] Childrens Hosp, Dept Anesthesiol, Boston, MA 02115 USA
[3] Univ Massachusetts, Sch Med, Dept Canc Biol, Worcester, MA USA
[4] Massachusetts Gen Hosp, Ctr Syst Biol, Boston, MA 02114 USA
[5] MIT, David H Koch Inst Integrat Canc Res, Cambridge, MA 02139 USA
来源
PLOS ONE | 2010年 / 5卷 / 03期
关键词
FOREIGN-BODY REACTION; ALGINATE; ISLETS; FIBROBLASTS; ARTHRITIS; TUMORS; SKIN;
D O I
10.1371/journal.pone.0010032
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Background: Many materials are unsuitable for medical use because of poor biocompatibility. Recently, advances in the high throughput synthesis of biomaterials has significantly increased the number of potential biomaterials, however current biocompatibility analysis methods are slow and require histological analysis. Methodology/Principal Findings: Here we develop rapid, non-invasive methods for in vivo quantification of the inflammatory response to implanted biomaterials. Materials were placed subcutaneously in an array format and monitored for host responses as per ISO 10993-6: 2001. Host cell activity in response to these materials was imaged kinetically, in vivo using fluorescent whole animal imaging. Data captured using whole animal imaging displayed similar temporal trends in cellular recruitment of phagocytes to the biomaterials compared to histological analysis. Conclusions/Significance: Histological analysis similarity validates this technique as a novel, rapid approach for screening biocompatibility of implanted materials. Through this technique there exists the possibility to rapidly screen large libraries of polymers in vivo.
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页数:8
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