Costantini Marco, Colosi Cristina, Guzowski Jan, Barbetta Andrea, Jaroszewicz Jakub, Swięszkowski Wojciech, Dentini Mariella, Garstecki Piotr
Department of Chemistry, Sapienza University of Rome, 00185 Rome, Italy.
J Mater Chem B. 2014 Apr 28;2(16):2290-2300. doi: 10.1039/c3tb21227k. Epub 2014 Mar 17.
We demonstrate how to generate highly ordered porous matrices from dextran-methacrylate (DEX-MA) using microfluidics. We use a flow focusing device to inject an aqueous solution of DEX-MA and surfactant to break the flow of an organic solvent (cyclohexane) into monodisperse droplets at a high volume fraction (above 74% v/v) to form an ordered high internal phase emulsion (HIPE). We collect the crystalline HIPE structure and freeze it by gelling. The resulting polyHIPEs are characterized by an interconnected and ordered morphology. The size of pores and interconnects ranges between hundreds and tens of micrometers, respectively. The technique that we describe allows for precise tuning of all the structural parameters of the matrices, including their porosity, the size of the pores and the lumen of interconnects between the pores. The resulting ordered and precisely tailored HIPE gels represent a new class of scaffolds for applications in tissue engineering.
我们展示了如何使用微流控技术从甲基丙烯酸葡聚糖(DEX-MA)生成高度有序的多孔基质。我们使用流动聚焦装置注入DEX-MA水溶液和表面活性剂,以将有机溶剂(环己烷)的流动在高体积分数(高于74% v/v)下破碎成单分散液滴,从而形成有序的高内相乳液(HIPE)。我们收集结晶的HIPE结构并通过凝胶化将其冷冻。所得的聚HIPE具有相互连接且有序的形态特征。孔和互连通道的尺寸分别在数百微米和数十微米之间。我们所描述的技术允许对基质的所有结构参数进行精确调整,包括其孔隙率、孔的大小以及孔之间互连通道的内腔。所得的有序且精确定制的HIPE凝胶代表了一类用于组织工程应用的新型支架。