4.8 Article

Single-Step Synthesis of Alginate Microgels Enveloped with a Covalent Polymeric Shell: A Simple Way to Protect Encapsulated Cells

Journal

ACS APPLIED MATERIALS & INTERFACES
Volume 13, Issue 16, Pages 18432-18442

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/acsami.0c20613

Keywords

microcapsules; core-shell structures; multilayered capsules; liquid-core capsules; cell encapsulation

Funding

  1. NSF [1844299, 1932963, 1805274]
  2. Directorate For Engineering
  3. Div Of Chem, Bioeng, Env, & Transp Sys [1932963, 1805274, 1844299] Funding Source: National Science Foundation

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Microgels of biopolymers such as alginate are commonly used for cell encapsulation. By enveloping alginate gels with a thin shell of a covalently cross-linked gel, the microcapsules become more robust and stable under various conditions, enabling long-term viability and functionality of encapsulated cells.
Microgels of biopolymers such as alginate are widely used to encapsulate cells and other biological payloads. Alginate is an attractive material for cell encapsulation because it is nontoxic and convenient: spherical alginate gels are easily created by contacting aqueous droplets of sodium alginate with divalent cations such as Ca2+. Alginate chains in the gel become crosslinked by Ca2+ cations into a 3-D network. When alginate gels are placed in a buffer, however, the Ca2+ cross-links are eliminated by exchange with Na+, thereby weakening and degrading the gels. With time, encapsulated cells are released into the external solution. Here, we describe a simple solution to the above problem, which involves forming alginate gels enveloped by a thin shell of a covalently cross-linked gel. The shell is formed via free-radical polymerization using conventional monomers such as acrylamide (AAm) or acrylate derivatives, including polyethylene glycol diacrylate (PEGDA). The entire process is performed in a single step at room temperature (or 37 degrees C) under mild, aqueous conditions. It involves combining the alginate solution with a radical initiator, which is then introduced as droplets into a reservoir containing Ca2+ and monomers. Within minutes of either simple incubation or exposure to ultraviolet (UV) light, the droplets are converted into alginate-polymer microcapsules with a core of alginate and a shell of the polymer (AAm or PEGDA). The microcapsules are mechanically more robust than conventional alginate/Ca2+ microgels, and while the latter swell and degrade when placed in buffers or in chelators like sodium citrate, the former remain stable under all conditions. We encapsulate both bacteria and mammalian cells in these microcapsules and find that the cells remain viable and functional over time. Lastly, a variation of the synthesis technique is shown to generate multilayered microcapsules with a liquid core surrounded by concentric layers of alginate and AAm gels. We anticipate that the approaches presented here will find application in a variety of areas including cell therapies, artificial cells, drug delivery, and tissue engineering.

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