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通过核心液滴之间的选择性聚结与超薄壳层相结合而形成的藻酸盐微凝胶。

Alginate microgels created by selective coalescence between core drops paired with an ultrathin shell.

作者信息

Lee Tae Yong, Praveenkumar Ramasamy, Oh You-Kwan, Lee Kyubock, Kim Shin-Hyun

机构信息

Department of Chemical and Biomolecular Engineering, KAIST, Daejeon 34141, Korea.

出版信息

J Mater Chem B. 2016 May 21;4(19):3232-3238. doi: 10.1039/c6tb00580b. Epub 2016 Apr 20.

DOI:10.1039/c6tb00580b
PMID:32263258
Abstract

We report a highly biocompatible and practical protocol to create alginate microgels for bioactive encapsulation. Double-emulsion drops composed of dual cores enclosed by an ultrathin shell are prepared in a capillary microfluidic device, which exhibit selective coalescence between the cores. When the cores are laden with alginate precursors and divalent ions, respectively, coalescence leads to the formation of alginate microgels in the fused core of double-emulsion drops. The microgel can be rapidly released into a continuous water phase by rupturing the liquid shell. This method neither involves any toxic chemical cues for gelation nor long-term exposure to oil, thereby providing highly biocompatible encapsulation.

摘要

我们报告了一种用于制备用于生物活性封装的藻酸盐微凝胶的高度生物相容性且实用的方案。在毛细管微流控装置中制备由超薄壳包裹的双核组成的双乳液滴,其在核之间表现出选择性聚结。当核分别负载藻酸盐前体和二价离子时,聚结导致在双乳液滴的融合核中形成藻酸盐微凝胶。通过破裂液壳,微凝胶可迅速释放到连续水相中。该方法既不涉及任何用于凝胶化的有毒化学线索,也不涉及长期暴露于油中,从而提供了高度生物相容性的封装。

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