Department of Materials Engineering, Isfahan University of Technology, Isfahan, 84156-83111, Iran.
Macromol Biosci. 2018 Jun;18(6):e1800020. doi: 10.1002/mabi.201800020. Epub 2018 Apr 27.
The combination of bioactive components such as calcium phosphates and fibrous structures are encouraging niche-mimetic keys for restoring bone defects. However, the importance of hemocompatibility of the membranes is widely ignored. Heparin-loaded nanocomposite poly(ε-caprolactone) (PCL)-α-tricalcium phosphate (α-TCP) fibrous membranes are developed to provide bioactive and hemocompatible constructs for bone tissue engineering. Nanocomposite membranes are optimized based on bioactivity, mechanical properties, and cell interaction. Consequently, various concentrations of heparin molecules are loaded within nanocomposite fibrous membranes. In vitro heparin release profiles reveal a sustained release of heparin over the period of 14 days without an initial burst. Moreover, heparin encapsulation enhances mesenchymal stem cell (MSC) attachment and proliferation, depending on the heparin content. It is concluded that the incorporation of heparin within TCP-PCL fibrous membranes provides the most effective cellular interactions through synergistic physical and chemical cues.
生物活性成分(如磷酸钙和纤维结构)的组合是恢复骨缺损的仿生学关键,这一点令人鼓舞。然而,人们广泛忽视了膜的血液相容性的重要性。本研究开发了载肝素的纳米复合聚(ε-己内酯)(PCL)-α-磷酸三钙(α-TCP)纤维膜,为骨组织工程提供了具有生物活性和血液相容性的构建体。基于生物活性、机械性能和细胞相互作用对纳米复合膜进行了优化。因此,将不同浓度的肝素分子载入纳米复合纤维膜中。体外肝素释放曲线显示肝素在 14 天内持续释放,没有初始突释。此外,肝素包封可促进间充质干细胞(MSC)的附着和增殖,这取决于肝素的含量。结论是,肝素的掺入使 TCP-PCL 纤维膜能够通过协同的物理和化学线索提供最有效的细胞相互作用。