School of Engineering, University of British Columbia, 3333 University Way, Kelowna, BC V1V 1V7, Canada; Center for Minimally Invasive Therapeutics (C-MIT), California NanoSystems Institute (CNSI), Department of Bioengineering, University of California - Los Angeles, 410 Westwood Plaza, Los Angeles, CA 90095, USA.
School of Engineering, University of British Columbia, 3333 University Way, Kelowna, BC V1V 1V7, Canada.
Acta Biomater. 2019 Sep 15;96:149-160. doi: 10.1016/j.actbio.2019.06.040. Epub 2019 Jun 25.
In the present study, polydimethylsiloxane (PDMS) porous scaffolds are designed based on minimal surface architectures and fabricated through a low-cost and accessible sacrificial mold printing approach using a fused deposition modeling (FDM) 3D printer. The effects of pore characteristics on compressive properties and fluid permeability are studied. The results suggest that radially gradient pore distribution (as a potential way to enhance mechanically-efficient scaffolds with enhanced cell/scaffold integration) has higher elastic modulus and fluid permeability compared to their uniform porosity counterparts. Also, the scaffolds are fairly strain-reversible under repeated loading of up to 40% strain. Among different triply periodic minimal surface pore architectures, P-surface was observed to be stiffer, less permeable and have lower densification strain compared to the D-surface and G-surface-based pore shapes. The biocompatibility of the created scaffolds is assessed by filling the PDMS scaffolds using mouse embryonic fibroblasts with cell-laden gelatin methacryloyl which was cross-linked in situ by UV light. Cell viability is found to be over 90% after 4 days in 3D culture. This method allows for effectively fabricating biocompatible porous organ-shaped scaffolds with detailed pore features which can potentially tailor tissue regenerative applications. STATEMENT OF SIGNIFICANCE: Printing polymers with chemical curing mechanism required for materials such as PDMS is challenging and impossible to create high-resolution uniformly cured structures due to hard control on the base polymer and curing process. An interconnected porous mold with ordered internal architecture with complex geometries were 3D printed using low-cost and accessible FDM technology. The mold acted as a 3D sacrificial material to form internally architected flexible PDMS scaffolds for tissue engineering applications. The scaffolds are mechanically stable under high strain cyclic loads and provide enough pore and space for viably integrating cells within the gradient architecture in a controllable manner.
在本研究中,基于最小曲面结构设计了聚二甲基硅氧烷(PDMS)多孔支架,并通过使用熔融沉积建模(FDM)3D 打印机的低成本且易于获得的牺牲模印刷方法制造。研究了孔特征对压缩性能和流体渗透性的影响。结果表明,与具有均匀孔隙率的对应物相比,径向梯度孔分布(作为增强细胞/支架整合的机械高效支架的潜在方法)具有更高的弹性模量和流体渗透性。此外,在高达 40%应变的重复加载下,支架具有相当的可恢复应变。在不同的三重周期性最小表面孔结构中,与 D 面和 G 面为基础的孔形状相比,P 面表现出更硬、渗透性更低且致密化应变更低。通过用原位交联的紫外光交联的载有细胞的明胶甲基丙烯酰来填充 PDMS 支架,评估了所创建支架的生物相容性。在 3D 培养中 4 天后,细胞活力超过 90%。这种方法允许有效地制造具有详细孔特征的生物相容多孔器官形状支架,这可能可以针对组织再生应用进行定制。意义声明:对于 PDMS 等需要化学固化机制的聚合物进行打印具有挑战性,并且由于难以控制基础聚合物和固化过程,因此不可能创建高分辨率的均匀固化结构。使用低成本且易于获得的 FDM 技术 3D 打印具有有序内部结构的互连多孔模具,具有复杂的几何形状。该模具充当 3D 牺牲材料,用于形成用于组织工程应用的内部结构的柔性 PDMS 支架。支架在高应变循环负载下机械稳定,并以可控制的方式为梯度结构内的细胞提供足够的孔和空间以实现可行的整合。