Polymers and Fiber Surfaces

聚合物和纤维表面

• 批准号: 270156600
• 负责人: Professor Dr. Henning Menzel
• 金额: --
• 依托单位: Department of Materials Science and Engineering
• 依托单位国家: 德国
• 项目类别: Research Units
• 财政年份: 2015
• 资助国家: 德国
• 起止时间: 2014-12-31 至 2022-12-31
• 项目状态: 已结题
• 来源: https://gepris.dfg.de/gepris/projekt/270156600?language=en
• 关键词: Polymers; Fiber; Surfaces

The starting point for the preparation of graded implants are fiber mats prepared by electrospinning of polycaprolacton (PCL). Aim of this project is, to modify the fiber mats in a way that they will be suited for the functionalization with drug release systems. To do so, the fiber mats are treated by plasma, coated with polydopamin (pDA) or with chitosan-graft-polycaprolacton (Chi-g-PCL). In the last grant period these three methods have been proven to be suitable to functionalize fiber mats with drug release systeme and to create spatial gradients. However, the different modifications differ in the results obtained. It was found that more nanoporous silica nanoparticles as drug release system could be adsorbed by the pDA modified fiber mats compared to those modified with Chi-g-PCL. However, less signaling protein was released from polymeric drug delivery systems on fiber mats modified with pDA compared to fiber mats modified with Chi-g-PCL. These differences and with that the advantages and disadvantages of the modification methods shall be investigated systematically. In addition they shall be ascribed to chemical and physical surface properties. To do so the differently modified fiber mats will be functionalized with the same drug release system (supplied by subproject TP5) and the release kinetics will be investigated (together with subproject TP6). The results will be correlated with the surface potential (zeta-Potential) of the modified fiber mats, which can be determined by electro-kinetic measurements. Besides the electrostatic interactions which can be quantified using the zeta potentials of the fiber surfaces, the drug release system and the proteins, also hydrophobic interactions will be taken into account. For this, protein adsorption measurements with model proteins will be carried out. A thorough understanding auf the electrostatic and hydrophobic interactions will enable a knowledge-based design of an optimal modification of the fiber mats. This will also will allow a transfer of the method to other biomedical applications. First tests to transfer the coating methods to other substrates will be carried out. Blending of PCL with different PCL-block- and graft-copolymers will be prepared and electro spun as blend. In this way, further methods to introduce further chemical functionalities at the surface which can be used to improve cell adhesion if necessary. Blending with photo-reactive copolymers shall be used to adjust the properties of the fibers (together with subproject TP3).

制备梯度植入物的起点是通过静电纺丝聚己内酯（PCL）制备的纤维垫。该项目的目的是，以一种适合于药物释放系统功能化的方式对纤维垫进行改性。为此，纤维垫通过等离子体处理，用聚多巴胺（pDA）或用壳聚糖-接枝-聚己内酯（Chi-g-PCL）涂覆。在上一个资助期内，这三种方法已被证明适用于用药物释放系统功能化纤维垫并产生空间梯度。然而，不同的修改在所获得的结果不同。结果表明，pDA改性的纤维毡比Chi-g-PCL改性的纤维毡能更好地吸附作为药物释放系统的纳米多孔二氧化硅纳米粒子。然而，与用Chi-g-PCL改性的纤维垫相比，用pDA改性的纤维垫上的聚合物药物递送系统释放的信号蛋白较少。应系统地研究这些差异以及修改方法的优点和缺点。此外，它们应归因于化学和物理表面特性。为此，将用相同的药物释放系统（由子项目TP 5提供）对不同改性的纤维垫进行功能化，并研究释放动力学（与子项目TP 6一起）。结果将与改性纤维垫的表面电位（zeta-电位）相关，该表面电位可以通过电动测量来确定。除了可以使用纤维表面、药物释放系统和蛋白质的ζ电位量化的静电相互作用之外，还将考虑疏水相互作用。为此，将使用模型蛋白质进行蛋白质吸附测量。深入了解静电和疏水相互作用将使基于知识的设计的纤维毡的最佳改性。这也将允许将该方法转移到其他生物医学应用中。将进行将涂层方法转移到其他基材上的第一次测试。将制备PCL与不同PCL嵌段共聚物和接枝共聚物的共混物并静电纺丝为共混物。以这种方式，如果需要，在表面引入可以用于改善细胞粘附的其他化学官能团的其他方法。应使用与光反应共聚物的混合来调整纤维的性能（与子项目TP 3一起）。