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利用离心法消除空微胶囊以制备用于芯片成像细胞分选仪的、与内容物大小相关的海藻酸盐微胶囊

Content Size-Dependent Alginate Microcapsule Formation Using Centrifugation to Eliminate Empty Microcapsules for On-Chip Imaging Cell Sorter Application.

作者信息

Akimoto Toshinosuke, Yasuda Kenji

机构信息

Department of Pure and Applied Physics, Graduate School of Advanced Science and Engineering, Waseda University, 3-4-1 Okubo, Shinjuku, Tokyo 169-8555, Japan.

Department of Physics, School of Advanced Science and Engineering, Waseda University, 3-4-1 Okubo, Shinjuku, Tokyo 169-8555, Japan.

出版信息

Micromachines (Basel). 2022 Dec 27;14(1):72. doi: 10.3390/mi14010072.

DOI:10.3390/mi14010072
PMID:36677133
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9867324/
Abstract

Alginate microcapsules are one of the attractive non-invasive platforms for handling individual cells and clusters, maintaining their isolation for further applications such as imaging cell sorter and single capsule qPCR. However, the conventional cell encapsulation techniques provide huge numbers of unnecessary empty homogeneous alginate microcapsules, which spend an excessive majority of the machine time on observations and analysis. Here, we developed a simple alginate cell encapsulation method to form content size-dependent alginate microcapsules to eliminate empty microcapsules using microcapillary centrifugation and filtration. Using this method, the formed calcium alginate microcapsules containing the HeLa cells were larger than 20m, and the other empty microcapsules were less than 3m under 4000 rpm centrifugation condition. We collected cell-containing alginate microcapsules by eliminating empty microcapsules from the microcapsule mixture with simple one-step filtration of a 20 m cell strainer. The electrical surface charge density and optical permeability of those cell-encapsulated alginate microcapsules were also evaluated. We found that the surface charge density of cell-encapsulated alginate microbeads is more than double that of cells, indicating that less voltage is required for electrical cell handling with thin alginate gel encapsulation of samples. The permeability of the alginate microcapsule was not improved by changing the reflective index of the medium buffer, such as adding alginate ester. However, the minimized thickness of the alginate gel envelope surrounding cells in the microcapsules did not degrade the detailed shapes of encapsulated cells. Those results confirmed the advantage of alginate encapsulation of cells with the centrifugation method as one of the desirable tools for imaging cell sorting applications.

摘要

藻酸盐微胶囊是用于处理单个细胞和细胞簇的有吸引力的非侵入性平台之一,可保持它们的隔离状态以用于进一步的应用,如成像细胞分选仪和单胶囊定量聚合酶链反应。然而,传统的细胞包封技术会产生大量不必要的空的均匀藻酸盐微胶囊,这使得机器在观察和分析上花费了过多的时间。在这里,我们开发了一种简单的藻酸盐细胞包封方法,以形成与内容物大小相关的藻酸盐微胶囊,通过微毛细管离心和过滤来消除空微胶囊。使用这种方法,在4000转/分钟的离心条件下,含有HeLa细胞的形成的海藻酸钙微胶囊大于20微米,而其他空微胶囊小于3微米。我们通过用20微米细胞筛网进行简单的一步过滤,从微胶囊混合物中去除空微胶囊,从而收集含细胞的藻酸盐微胶囊。还评估了那些细胞包封的藻酸盐微胶囊的表面电荷密度和光学渗透率。我们发现,细胞包封的藻酸盐微珠的表面电荷密度是细胞的两倍多,这表明在用薄藻酸盐凝胶包封样品进行细胞电处理时所需的电压更低。通过改变介质缓冲液的折射率,如添加藻酸酯,藻酸盐微胶囊的渗透率并没有提高。然而,微胶囊中围绕细胞的藻酸盐凝胶包膜的最小厚度并没有降低包封细胞的详细形状。这些结果证实了采用离心法进行藻酸盐细胞包封作为成像细胞分选应用的理想工具之一的优势。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/86a9/9867324/cb31e85903a5/micromachines-14-00072-g014.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/86a9/9867324/1fd3a2e98a62/micromachines-14-00072-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/86a9/9867324/4b402be8f296/micromachines-14-00072-g002a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/86a9/9867324/673872a56455/micromachines-14-00072-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/86a9/9867324/a68aba8e0bbf/micromachines-14-00072-g004a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/86a9/9867324/d373a7c569a0/micromachines-14-00072-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/86a9/9867324/c97c09075b7d/micromachines-14-00072-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/86a9/9867324/4e000195592e/micromachines-14-00072-g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/86a9/9867324/057d287b3713/micromachines-14-00072-g008.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/86a9/9867324/0bd1657c57f4/micromachines-14-00072-g009.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/86a9/9867324/e281ec4dbca5/micromachines-14-00072-g010.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/86a9/9867324/152e654bad67/micromachines-14-00072-g011.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/86a9/9867324/cf1d59f46b69/micromachines-14-00072-g012.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/86a9/9867324/f795df3242a8/micromachines-14-00072-g013.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/86a9/9867324/cb31e85903a5/micromachines-14-00072-g014.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/86a9/9867324/1fd3a2e98a62/micromachines-14-00072-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/86a9/9867324/4b402be8f296/micromachines-14-00072-g002a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/86a9/9867324/673872a56455/micromachines-14-00072-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/86a9/9867324/a68aba8e0bbf/micromachines-14-00072-g004a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/86a9/9867324/d373a7c569a0/micromachines-14-00072-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/86a9/9867324/c97c09075b7d/micromachines-14-00072-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/86a9/9867324/4e000195592e/micromachines-14-00072-g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/86a9/9867324/057d287b3713/micromachines-14-00072-g008.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/86a9/9867324/0bd1657c57f4/micromachines-14-00072-g009.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/86a9/9867324/e281ec4dbca5/micromachines-14-00072-g010.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/86a9/9867324/152e654bad67/micromachines-14-00072-g011.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/86a9/9867324/cf1d59f46b69/micromachines-14-00072-g012.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/86a9/9867324/f795df3242a8/micromachines-14-00072-g013.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/86a9/9867324/cb31e85903a5/micromachines-14-00072-g014.jpg

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