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Controlled microfluidic production of alginate beads for in situ encapsulation of microbes

机译:海藻酸盐珠粒的微流控生产,用于微生物的原位包封

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The development and refinement of a microfluidic-based alginate bead generator system for bacterial encapsulation is presented. The resulting microgels have application for the encapsulation of single cells, and can allow for small scale, clonal expansion of thousands of isolated cells in parallel. PDMS based microfluidic chips were fabricated using conventional lithography techniques to produce both externally gelled and directly gelled alginate microspheres using a controlled, water-in-oil emulsion system. The production of directly gelled beads, formed by the in-chip mixing of aqueous alginate and calcium chloride solutions dispersed within an organic carrier flowstream is qualitatively compared to a system, which produces beads and relies on diffusion of a crosslinking agent from the carrier fluid to cause gelation (external gelation). While the direct gelation scheme allows the use of biocompatible oils as the organic carrier, it also has a detrimental effect on device stability often resulting in clogging and gel-streaming at the microfluidic interface of these solutions. A design for the continuous production of directly gelled beads was evaluated in terms of the threshold flow conditions and reagent concentrations that did not result in clogging or streaming. Monodisperse alginate microgels of 30 mum diameter were produced at frequencies of over 500 beads per second. The beads could be completely dispersed into aqueous media using an off-chip washing protocol to remove the organic phase. The microgels effectively encapsulated individual or small numbers of GFP-expressing Escherichia. coli, which could be subsequently clonally expanded. The described microfluidic platform is a robust front-end sample preparation technology that shows strong potential for use in drug delivery systems, biosensors, and other cell-based microcompartmentalization applications. The co-culturing of microbial colonies in a large population of alginate beads will allow for functional -nsorting and genetic analyses at the single cell level.
机译:介绍了用于微囊化的微流体藻酸盐微珠发生器系统的开发和完善。所得的微凝胶可用于包封单个细胞,并且可允许成千上万个并行分离细胞的小规模克隆扩增。使用常规光刻技术制造基于PDMS的微流控芯片,以使用可控的油包水型乳化液系统生产外部胶化和直接胶化的藻酸盐微球。与分散在有机载体流中的藻酸盐水溶液和氯化钙溶液的芯片内混合形成的直接胶凝珠的生产相比,系统的定性比较高,该系统产生珠并依靠交联剂从载液扩散到引起胶凝(外部胶凝)。虽然直接凝胶化方案允许使用生物相容性油作为有机载体,但它对设备的稳定性也有不利影响,通常会导致这些溶液的微流体界面处发生堵塞和凝胶流。根据阈值流动条件和不会导致堵塞或流动的试剂浓度,评估了连续生产直接胶凝珠的设计。以每秒超过500个珠的频率生产直径为30微米的单分散藻酸盐微凝胶。可以使用芯片外洗涤方案将珠子完全分散到水性介质中,以去除有机相。微凝胶有效地包封了个别或少量表达GFP的大肠杆菌。大肠杆菌,随后可以克隆扩增。所描述的微流体平台是一种强大的前端样品制备技术,显示出在药物输送系统,生物传感器和其他基于细胞的微区室化应用中的强大潜力。在大量藻酸盐珠粒中共同培养微生物菌落将允许在单个细胞水平上进行功能分类和遗传分析。

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