Faley Shannon L, Baer Bradly B, Larsen Taylor S H, Bellan Leon M
Department of Mechanical Engineering, Vanderbilt University , 2400 Highland Avenue, 101 Olin Hall, Nashville, Tennessee 37212, USA.
Biomicrofluidics. 2015 May 20;9(3):036501. doi: 10.1063/1.4921453. eCollection 2015 May.
Biomimetic scaffolds approaching physiological scale, whose size and large cellular load far exceed the limits of diffusion, require incorporation of a fluidic means to achieve adequate nutrient/metabolite exchange. This need has driven the extension of microfluidic technologies into the area of biomaterials. While construction of perfusable scaffolds is essentially a problem of microfluidic device fabrication, functional implementation of free-standing, thick-tissue constructs depends upon successful integration of external pumping mechanisms through optimized connective assemblies. However, a critical analysis to identify optimal materials/assembly components for hydrogel substrates has received little focus to date. This investigation addresses this issue directly by evaluating the efficacy of a range of adhesive and mechanical fluidic connection methods to gelatin hydrogel constructs based upon both mechanical property analysis and cell compatibility. Results identify a novel bioadhesive, comprised of two enzymatically modified gelatin compounds, for connecting tubing to hydrogel constructs that is both structurally robust and non-cytotoxic. Furthermore, outcomes from this study provide clear evidence that fluidic interconnect success varies with substrate composition (specifically hydrogel versus polydimethylsiloxane), highlighting not only the importance of selecting the appropriately tailored components for fluidic hydrogel systems but also that of encouraging ongoing, targeted exploration of this issue. The optimization of such interconnect systems will ultimately promote exciting scientific and therapeutic developments provided by microfluidic, cell-laden scaffolds.
接近生理尺度的仿生支架,其尺寸和大量细胞负载远远超过扩散极限,需要采用流体手段来实现充足的营养物质/代谢产物交换。这种需求推动了微流控技术向生物材料领域的扩展。虽然可灌注支架的构建本质上是一个微流控设备制造问题,但独立的厚组织构建体的功能实现取决于通过优化连接组件成功整合外部泵送机制。然而,迄今为止,针对水凝胶基质确定最佳材料/组装组件的关键分析很少受到关注。本研究通过基于力学性能分析和细胞相容性评估一系列用于明胶水凝胶构建体的粘合剂和机械流体连接方法的功效,直接解决了这个问题。结果确定了一种新型生物粘合剂,由两种酶促修饰的明胶化合物组成,用于将管道连接到水凝胶构建体,该粘合剂在结构上坚固且无细胞毒性。此外,本研究结果提供了明确证据,表明流体互连的成功与否因基质组成(特别是水凝胶与聚二甲基硅氧烷)而异,这不仅突出了为流体水凝胶系统选择适当定制组件的重要性,也强调了鼓励对此问题进行持续、有针对性探索的重要性。这种互连系统的优化最终将推动微流控、负载细胞支架带来的令人兴奋的科学和治疗进展。