期刊
AAPS JOURNAL
卷 12, 期 2, 页码 188-196出版社
SPRINGER
DOI: 10.1208/s12248-010-9175-3
关键词
biocompatible coating for implantable devices; foreign body response (FBR); glucose biosensor; tissue compatibility assessment; drug device combination products
资金
- TATRC [W81XWH0710688]
- NIH [R21HL90458-01]
- U.S. Department of Defense (DOD) [W81XWH0710688] Funding Source: U.S. Department of Defense (DOD)
In recent years, a variety of biomaterial implantable devices has been developed. Of particular significance to pharmaceutical sciences is the progress made on the development of drug/implantable device combination products. However, the clinical application of these devices is still a critical issue due to the host response, which results from both the tissue trauma during implantation and the presence of the device in the body. Accordingly, the in vivo functionality and durability of any implantable device can be compromised by the body response to the foreign material. Numerous strategies to overcome negative body reactions have been reported. The aim of this review is to outline some key issues of biomaterial/tissue interactions such as foreign body response and biocompatibility and biocompatibility assessment. In addition, general approaches used to overcome the in vivo instability of implantable devices are presented, including (a) biocompatible material coatings, (b) steroidal and nonsteroidal anti-inflammatory drugs, and (c) angiogenic drugs. In particular, strategies to overcome host response to glucose biosensors are summarized.
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