LaBS, Department of Structural Engineering, Politecnico di Milano, Milan, Italy.
Biomed Microdevices. 2012 Feb;14(1):225-34. doi: 10.1007/s10544-011-9600-0.
Perfusion bioreactors are widely used in tissue engineering and pharmaceutical research to provide reliable models of tissue growth under controlled conditions. Destructive assays are not able to follow the evolution of the growing tissue on the same construct, so it is necessary to adopt non-destructive analysis. We have developed a miniaturized, optically accessible bioreactor for interstitial perfusion of 3D cell-seeded scaffolds. The scaffold adopted was optically transparent, with highly defined architecture. Computational fluid dynamics (CFD) analysis was useful to predict the flow behavior in the bioreactor scaffold chamber (that was laminar flow, Re = 0.179, with mean velocity equal to 100 microns/s). Moreover, experimental characterization of the bioreactor performance gave that the maximum allowable pressure was 0.06 MPa and allowable flow rate up to 25 ml/min. A method, to estimate quantitatively and non destructively the cell proliferation (from 15 to 43 thousand cells) and tissue growth (from 2% to 43%) during culture time, was introduced and validated. An end point viability test was performed to check the experimental set-up overall suitability for cell culture with successful results. Morphological analysis was performed at the end time point to show the complex tridimensional pattern of the biological tissue growth. Our system, characterized by controlled conditions in a wide range of allowable flow rate and pressure, permits to systematically study the influence of several parameters on engineered tissue growth, using viable staining and a standard fluorescence microscope.
灌注式生物反应器广泛应用于组织工程和药物研究领域,可在受控条件下提供可靠的组织生长模型。破坏性分析无法在同一构建体上跟踪生长组织的演变,因此需要采用非破坏性分析。我们开发了一种小型化、光学可访问的三维细胞接种支架间质灌注式生物反应器。所采用的支架具有光学透明性和高度定义的结构。计算流体动力学 (CFD) 分析有助于预测生物反应器支架腔中的流动行为(层流,Re=0.179,平均速度等于 100 微米/秒)。此外,对生物反应器性能的实验表征表明,最大允许压力为 0.06 MPa,允许流速高达 25 ml/min。引入并验证了一种方法,可定量且非破坏性地估计培养过程中的细胞增殖(从 15 到 43 千个细胞)和组织生长(从 2%到 43%)。进行了终点存活试验以检查细胞培养的整个实验设置的适用性,结果令人满意。在实验结束时进行形态分析,以显示生物组织生长的复杂三维模式。我们的系统具有可在广泛允许流速和压力范围内进行控制的特点,允许使用活细胞染色和标准荧光显微镜系统地研究各种参数对工程组织生长的影响。