Sohier J, Vlugt T J H, Cabrol N, Van Blitterswijk C, de Groot K, Bezemer J M
OctoPlus, Zernikedreef 12, 2333 CL, Leiden, The Netherlands.
J Control Release. 2006 Mar 10;111(1-2):95-106. doi: 10.1016/j.jconrel.2005.11.016. Epub 2006 Feb 7.
To create porous scaffolds releasing in a controlled and independent fashion two different proteins, a novel approach based on protein-loaded polymeric coatings was evaluated. In this process, two water-in-oil emulsions are forced successively through a prefabricated scaffold to create coatings, containing each a different protein and having different release characteristics. In a first step, a simplified three-layered system was designed with model proteins (myoglobin and lysozyme). Poly(ether-ester) multiblock copolymers were chosen as polymer matrix, to allow the diffusion of proteins through the coatings. The model system showed the independent release of the two proteins. The myoglobin release was tailored from a burst to a linear release still on-going after 60 days, while the lysozyme release rate was kept constant. Macro-porous scaffolds, with a porosity of 59 vol.%, showed the same ability to control the release rate of the model proteins independently. The relation between the coatings properties and their release characteristics were investigated with the use of a mathematical diffusion model based on Fick's second law. It confirmed that the multiple coated scaffolds are biphasic system, where each coating controls the release of the protein that it contains. This approach could be of value for tissue engineering applications.
为了制备能够以可控且独立的方式释放两种不同蛋白质的多孔支架,对一种基于负载蛋白质的聚合物涂层的新方法进行了评估。在此过程中,将两种油包水乳液依次压过预制支架以形成涂层,每个涂层含有一种不同的蛋白质且具有不同的释放特性。第一步,用模型蛋白(肌红蛋白和溶菌酶)设计了一个简化的三层系统。选择聚(醚 - 酯)多嵌段共聚物作为聚合物基质,以使蛋白质能够通过涂层扩散。该模型系统显示出两种蛋白质的独立释放。肌红蛋白的释放从突发释放调整为线性释放,60天后仍在持续,而溶菌酶的释放速率保持恒定。孔隙率为59体积%的大孔支架显示出同样能够独立控制模型蛋白释放速率的能力。利用基于菲克第二定律的数学扩散模型研究了涂层性质与其释放特性之间的关系。结果证实,多层涂层支架是双相系统,其中每个涂层控制其所包含蛋白质的释放。这种方法可能对组织工程应用具有价值。