血管生成
治疗性血管生成
药物输送
血管生成
再生(生物学)
药品
癌症研究
药理学
生物
医学
计算生物学
新生血管
细胞生物学
纳米技术
干细胞
材料科学
祖细胞
作者
Wei Zhao,Eugenia Volkova,Michael R. Blatchley,Sharon Gerecht
标识
DOI:10.1016/j.addr.2019.08.005
摘要
In recent years, as the mechanisms of vasculogenesis and angiogenesis have been uncovered, the functions of various pro-angiogenic growth factors (GFs) and cytokines have been identified. Therefore, therapeutic angiogenesis, by delivery of GFs, has been sought as a treatment for many vascular diseases. However, direct injection of these protein drugs has proven to have limited clinical success due to their short half-lives and systemic off-target effects. To overcome this, hydrogel carriers have been developed to conjugate single or multiple GFs with controllable, sustained, and localized delivery. However, these attempts have failed to account for the temporal complexity of natural angiogenic pathways, resulting in limited therapeutic effects. Recently, the emerging ideas of optimal sequential delivery of multiple GFs have been suggested to better mimic the biological processes and to enhance therapeutic angiogenesis. Incorporating sequential release into drug delivery platforms will likely promote the formation of neovasculature and generate vast therapeutic potential.
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