Cryoprotection and banking of living cells in a 3D multiple emulsion‐based carrier

The ability to preserve stem cells/cells with minimal damage for short and long periods of time is essential for advancements in biomedical therapies and biotechnology. New methods of cell banking are continuously needed to provide effective damage prevention to cells. This paper puts forward a solu...

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Veröffentlicht in:Biotechnology journal 2017-08, Vol.12 (8), p.n/a
Hauptverfasser: Dluska, Ewa, Cui, Zhanfeng, Markowska‐Radomska, Agnieszka, Metera, Agata, Kosicki, Konrad
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Sprache:eng
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Zusammenfassung:The ability to preserve stem cells/cells with minimal damage for short and long periods of time is essential for advancements in biomedical therapies and biotechnology. New methods of cell banking are continuously needed to provide effective damage prevention to cells. This paper puts forward a solution to the problem of the low viability of cells during cryopreservation in a traditional suspension and storage by developing innovative multiple emulsion‐based carriers for the encapsulation and cryopreservation of cells. During freezing‐thawing processes, irreversible damage to cells occurs as a result of the formation of ice crystals, cell dehydration, and the toxicity of cryoprotectant. The proposed method was effective due to the “flexible” protective structure of multiple emulsions, which was proven by a high cell survival rate, above 90%. Results make new contributions in the fields of cell engineering and biotechnology and contribute to the development of methods for banking biological material. One of the key elements of cellular therapies is the process of banking cells. Traditionally, cells are frozen in aqueous suspensions at −196°C, which leads to low quality and viability of cells. To prevent cellular damage from ice crystals and toxicity of cryoprotectants, the authors propose the encapsulation of cells in the internal droplets of water‐in‐oil‐in‐water emulsions before freezing‐thawing processes.
ISSN:1860-6768
1860-7314
DOI:10.1002/biot.201600692