Sakiyama-Elbert Shelly E
Department of Biomedical Engineering, Washington University, 1 Brookings Drive, Campus Box 1097, St Louis, MO 63130, USA.
Acta Biomater. 2014 Apr;10(4):1581-7. doi: 10.1016/j.actbio.2013.08.045. Epub 2013 Sep 8.
This review provides an overview of the incorporation of heparin into biomaterials with a focus on drug delivery and the use of heparin-based biomaterials for self-assembly of polymer networks. Heparin conjugation to biomaterials was originally explored to reduce the thrombogenicity of materials in contact with blood. Many of the conjugation strategies that were developed for these applications are still popular today for other applications. More recently heparin has been conjugated to biomaterials for drug delivery applications. Many of the delivery approaches have taken advantage of the ability of heparin to bind to a wide variety of growth factors, protecting them from degradation and potentiating interactions with cell surface receptors. More recently, the use of heparin as a base polymer for scaffold fabrication has also been explored, often utilizing non-covalent binding of heparin with peptides or proteins to promote self-assembly of hydrogel networks. This review will highlight recent advances in each of these areas.
本综述概述了肝素在生物材料中的应用,重点关注药物递送以及基于肝素的生物材料在聚合物网络自组装中的应用。肝素与生物材料的结合最初是为了降低与血液接触的材料的血栓形成性。为这些应用开发的许多结合策略如今在其他应用中仍然很受欢迎。最近,肝素已与生物材料结合用于药物递送应用。许多递送方法利用了肝素与多种生长因子结合的能力,保护它们免受降解并增强与细胞表面受体的相互作用。最近,肝素作为支架制造的基础聚合物的应用也得到了探索,通常利用肝素与肽或蛋白质的非共价结合来促进水凝胶网络的自组装。本综述将重点介绍这些领域的最新进展。