去铁胺
再生(生物学)
伤口愈合
药理学
氧化应激
体内
炎症
药物输送
抗氧化剂
细胞生物学
医学
化学
免疫学
生物
生物化学
生物技术
有机化学
作者
Paige Holden,Lakshmi S. Nair
出处
期刊:Tissue Engineering Part B-reviews
[Mary Ann Liebert, Inc.]
日期:2019-06-11
卷期号:25 (6): 461-470
被引量:113
标识
DOI:10.1089/ten.teb.2019.0111
摘要
Deferoxamine (DFO) has been in use for half a century as a Food and Drug Administration-approved iron chelator, but recent studies indicate a variety of properties that could expand this drug's application into the fields of tissue and regenerative engineering. DFO has been implicated as an angiogenic agent in studies on ischemia, wound healing, and bone regeneration because of its ability to upregulate hypoxia-inducible factor-1 alpha (HIF-1α) and other key downstream angiogenic factors. DFO has also demonstrated antioxidant capabilities unrelated to its iron-chelating properties, making it a potential modulator of the oxidative stress involved in the inflammation response. Together, these properties make DFO a potential bioactive molecule to promote wound healing and enhance tissue integration of biomaterials in vivo. Deferoxamine (DFO) is approved by the Food and Drug Administration as an iron chelator and is been used to treat iron overload. Recent studies indicate that DFO may have important applications in the growing field of tissue regeneration because of its unique properties of downregulating inflammation while promoting vascularization, thereby enhancing wound healing in vivo.
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