Cell microencapsulation with synthetic polymers

The encapsulation of cells into polymeric microspheres or microcapsules has permitted the transplantation of cells into human and animal subjects without the need for immunosuppressants. Cell‐based therapies use donor cells to provide sustained release of a therapeutic product, such as insulin, and...

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Bibliographic Details
Published inJournal of biomedical materials research. Part A Vol. 103; no. 2; pp. 846 - 859
Main Author Olabisi, Ronke M.
Format Journal Article
LanguageEnglish
Published United States Blackwell Publishing Ltd 01.02.2015
Wiley Subscription Services, Inc
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Summary:The encapsulation of cells into polymeric microspheres or microcapsules has permitted the transplantation of cells into human and animal subjects without the need for immunosuppressants. Cell‐based therapies use donor cells to provide sustained release of a therapeutic product, such as insulin, and have shown promise in treating a variety of diseases. Immunoisolation of these cells via microencapsulation is a hotly investigated field, and the preferred material of choice has been alginate, a natural polymer derived from seaweed due to its gelling conditions. Although many natural polymers tend to gel in conditions favorable to mammalian cell encapsulation, there remain challenges such as batch to batch variability and residual components from the original source that can lead to an immune response when implanted into a recipient. Synthetic materials have the potential to avoid these issues; however, historically they have required harsh polymerization conditions that are not favorable to mammalian cells. As research into microencapsulation grows, more investigators are exploring methods to microencapsulate cells into synthetic polymers. This review describes a variety of synthetic polymers used to microencapsulate cells. © 2014 Wiley Periodicals, Inc. J Biomed Mater Res Part A: 103A: 846–859, 2015.
Bibliography:ark:/67375/WNG-M9RB2423-0
ArticleID:JBMA35205
istex:B63AE47F86DF51AEA311F0AF8D636ECF8F20DA07
ObjectType-Article-1
SourceType-Scholarly Journals-1
ObjectType-Feature-2
content type line 14
ObjectType-Review-3
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ISSN:1549-3296
1552-4965
1552-4965
DOI:10.1002/jbm.a.35205