Zhang Ge, Suggs Laura J
Department of Biomedical Engineering, University of Texas at Austin, 1 University Station C0800, Austin, TX 78712, USA.
Adv Drug Deliv Rev. 2007 May 30;59(4-5):360-73. doi: 10.1016/j.addr.2007.03.018. Epub 2007 Apr 18.
The purpose of this review is to give an overview of strategies using natural and artificial substrates to present active biomolecules in the development of vascular structures. Two primary topics are discussed. The first is the replacement and augmentation of arteries using vascular grafts or stents. Second is the recruitment of microvasculature secondary to an ischemic event or for the purpose of developing perfused, large-volume tissue-engineered constructs. Significant overlap exists among these topics. The focus is therefore on specific drug delivery strategies with discussion of a number of emerging themes. Where applicable, results from clinical trials have been included. Early work in the field includes covalent and nonspecific immobilization of growth factors, while more recent work emphasizes biologically inspired control over localization and temporal presentation. Novel strategies for matrix-mediated release can deliver multiple growth factors and/or cells in a manner that mimics tissue development and healing. Challenges that remain within this field center on controlling reciprocal interactions among the three fundamental tissue engineering components of scaffolds, cells and signals.
本综述的目的是概述在血管结构发育中使用天然和人工基质来呈现活性生物分子的策略。讨论了两个主要主题。第一个是使用血管移植物或支架替代和增强动脉。第二个是继发于缺血事件或为了开发灌注的、大容量组织工程构建体而募集微血管。这些主题之间存在显著重叠。因此,重点是特定的药物递送策略,并讨论了一些新出现的主题。在适用的情况下,纳入了临床试验结果。该领域的早期工作包括生长因子的共价和非特异性固定,而最近的工作则强调对定位和时间呈现的生物启发控制。基质介导释放的新策略可以以模仿组织发育和愈合的方式递送多种生长因子和/或细胞。该领域仍然存在的挑战集中在控制支架、细胞和信号这三个基本组织工程组件之间的相互作用。