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Deterministic Lateral Displacement as a Means to Enrich Large Cells for Tissue Engineering

机译:确定性侧向移位作为富集组织工程大细胞的手段

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The enrichment or isolation of selected cell types from heterogeneous suspensions is required in the area of tissue engineering. State of the art techniques utilized for this separation include preplating and sieve-based approaches that have limited ranges of purity and variable yield. Here, we present a deterministic lateral displacement (DLD) microfluidic device that is capable of separating large epithelial cells (17.3 +- 2.7 in diameter) from smaller fibroblast cells (13.7 +- 3.0 (mu)m in diameter) as a potential alternative approach. The mixed suspension examined is intended to represent the content of digested rat cardiac tissue, which contains equal proportions of cardiomyocyte (17.0 +- 4.0 (mu)m diameter) and nonmyocyte populations (12.0 +- 3.0 (mu)m diameter). High purity separation (> 97percent) of the larger cell type is achieved with 90percent yield in a rapid and single-pass process. The significance of this work lies in the recognition that DLD design principles can be applied for the microfluidic enrichment of large cells, up to the 40 (mu)m diameter level examined in this work.
机译:在组织工程领域中需要从异质悬浮液中富集或分离所选细胞类型。用于这种分离的最新技术包括纯度有限且产率可变的基于预镀和基于筛的方法。在这里,我们介绍一种确定性的侧向位移(DLD)微流体装置,该装置能够将较大的上皮细胞(直径为17.3±2.7)与较小的成纤维细胞(直径为13.7±3.0μm)分开,作为一种潜在的替代方法。所检查的混合悬浮液旨在代表消化的大鼠心脏组织的含量,其包含相等比例的心肌细胞(直径为17.0±4.0微米)和非肌细胞群体(直径为12.0±3.0微米)。通过快速,单次通过的过程,可以实现较大细胞类型的高纯度分离(> 97%),产率为90%。这项工作的意义在于认识到DLD设计原理可以应用于大细胞的微流体富集,在这项工作中所检查的直径水平最高可达40μm。

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