School of Mechanical, Materials, Mechatronic and Biomedical Engineering, University of Wollongong, Wollongong, NSW 2522, Australia.
Department of Chemistry, University of Tokyo, Tokyo, Japan.
Lab Chip. 2019 Sep 7;19(17):2811-2821. doi: 10.1039/c9lc00482c. Epub 2019 Jul 17.
Microalgae cells have been recognized as a promising sustainable resource to meet worldwide growing demands for renewable energy, food, livestock feed, water, cosmetics, pharmaceuticals, and materials. In order to ensure high-efficiency and high-quality production of biomass, biofuel, or bio-based products, purification procedures prior to the storage and cultivation of the microalgae from contaminated bacteria are of great importance. The present work proposed and developed a simple, sheathless, and efficient method to separate microalgae Chlorella from bacteria Bacillus Subtilis in a straight channel using the viscoelasticity of the medium. Microalgae and bacteria migrate to different lateral positions closer to the channel centre and channel walls respectively. Fluorescent microparticles with 1 μm and 5 μm diameters were first used to mimic the behaviours of bacteria and microalgae to optimize the separating conditions. Subsequently, size-based separation in Newtonian fluid and in viscoelastic fluid in straight channels with different aspect ratios was compared and demonstrated. Under the optimal condition, the removal ratio for 1 μm microparticles and separation efficiency for 5 μm particles can reach up to 98.28% and 93.85% respectively. For bacteria and microalgae cells separation, the removal ratio for bacteria and separation efficiency for microalgae cells is 92.69% and 100% respectively. This work demonstrated the continuous and sheathless separation of microalgae from bacteria for the first time by viscoelastic microfluidics. This technique can also be applied as an efficient and user-friendly method to separate mammalian cells or other kinds of cells.
微藻细胞已被认为是一种有前途的可持续资源,可以满足全球对可再生能源、食品、牲畜饲料、水、化妆品、药品和材料日益增长的需求。为了确保高效、高质量地生产生物质、生物燃料或基于生物的产品,在储存和培养微藻之前,对受污染细菌进行净化处理非常重要。本工作提出并开发了一种简单、无鞘、高效的方法,利用介质的粘弹性,在直通道中从枯草芽孢杆菌中分离小球藻。微藻和细菌分别迁移到靠近通道中心和通道壁的不同横向位置。首先使用直径为 1 μm 和 5 μm 的荧光微球来模拟细菌和微藻的行为,以优化分离条件。随后,比较并演示了在牛顿流体和粘弹性流体中,在不同纵横比的直通道中进行基于尺寸的分离。在最佳条件下,1 μm 微球的去除率和 5 μm 颗粒的分离效率分别可达 98.28%和 93.85%。对于细菌和微藻细胞的分离,细菌的去除率和微藻细胞的分离效率分别为 92.69%和 100%。本工作首次通过粘弹性微流控技术连续、无鞘地分离微藻和细菌。该技术还可以作为一种高效、易用的方法,用于分离哺乳动物细胞或其他类型的细胞。