MOE Key Laboratory of Macromolecule Synthesis and Functionalization, Department of Polymer Science and Engineering, Zhejiang University, Hangzhou 310027, China.
ACS Appl Mater Interfaces. 2021 Dec 8;13(48):57000-57008. doi: 10.1021/acsami.1c18333. Epub 2021 Nov 24.
Porous surfaces have attracted tremendous interest for customized incorporation of functional agents on biomedical devices. However, the versatile preparation of porous structures on complicated devices remains challenging. Herein, we proposed a simple and robust method to fabricate "spongy skin" on diversified polymeric substrates based on non-solvent-induced phase separation (NIPS). Through the swelling and the subsequent phase separation process, interconnected porous structures were directly formed onto the polymeric substrates. The thickness and pore size could be regulated in the ranges of 5-200 and 0.3-0.75 μm, respectively. The fast capillary action of the porous structure enabled controllable loading and sustained release of ofloxacin and bovine albumin at a high loading dosage of 79.9 and 24.1 μg/cm, respectively. We verified that this method was applicable to diversified materials including polymethyl methacrylate, polystyrene, thermoplastic polyurethane, polylactide acid, and poly(lactic--glycolic acid) and can be realized onto TCPS cell culture plates. This NIPS-based method is promising to generate porous surfaces on medical devices for incorporating therapeutic agents.
多孔表面因其在生物医学设备上定制功能性试剂方面的应用而受到极大关注。然而,在复杂设备上制备多功能的多孔结构仍然具有挑战性。在此,我们提出了一种基于非溶剂诱导相分离(NIPS)的简单且强大的方法,可在各种聚合物基底上制备“海绵状表皮”。通过溶胀和随后的相分离过程,可在聚合物基底上直接形成相互连接的多孔结构。厚度和孔径可分别在 5-200 μm 和 0.3-0.75 μm 的范围内调节。多孔结构的快速毛细作用可实现对氧氟沙星和牛血清白蛋白的可控负载和持续释放,载药剂量分别高达 79.9 和 24.1 μg/cm。我们验证了该方法适用于包括聚甲基丙烯酸甲酯、聚苯乙烯、热塑性聚氨酯、聚乳酸酸和聚(乳酸-乙醇酸)在内的多种材料,并且可以在 TCPS 细胞培养板上实现。这种基于 NIPS 的方法有望在医疗设备上生成多孔表面,以结合治疗剂。