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dc.contributor.authorJohnson, Amy S.
dc.contributor.authorO'Sullivan, Esther
dc.contributor.authorD'Aoust, Laura N.
dc.contributor.authorOmer, Abdulkadir
dc.contributor.authorBonner-Weir, Susan
dc.contributor.authorFisher, Robert J.
dc.contributor.authorWeir, Gordon C.
dc.contributor.authorColton, Clark K.
dc.date.accessioned2011-09-29T21:37:36Z
dc.date.available2011-09-29T21:37:36Z
dc.date.issued2011-04
dc.identifier.issn1937-3392
dc.identifier.urihttp://hdl.handle.net/1721.1/66121
dc.description.abstractImproved methods have recently been developed for assessing islet viability and quantity in human islet preparations for transplantation, and these measurements have proven useful for predicting transplantation outcome. The objectives of this study were to adapt these methods for use with microencapsulated islets, to verify that they provide meaningful quantitative measurements, and to test them with two model systems: (1) barium alginate and (2) barium alginate containing a 70% (w/v) perfluorocarbon (PFC) emulsion, which presents challenges to use of these assays and is of interest in its own right as a means for reducing oxygen supply limitations to encapsulated tissue. Mitochondrial function was assessed by oxygen consumption rate measurements, and the analysis of data was modified to account for the increased solubility of oxygen in the PFC-alginate capsules. Capsules were dissolved and tissue recovered for nuclei counting to measure the number of cells. Capsule volume was determined from alginate or PFC content and used to normalize measurements. After low oxygen culture for 2 days, islets in normal alginate lost substantial viable tissue and displayed necrotic cores, whereas most of the original oxygen consumption rate was recovered with PFC alginate, and little necrosis was observed. All nuclei were recovered with normal alginate, but some nuclei from nonrespiring cells were lost with PFC alginate. Biocompatibility tests revealed toxicity at the islet periphery associated with the lipid emulsion used to provide surfactants during the emulsification process. We conclude that these new assay methods can be applied to islets encapsulated in materials as complex as PFC-alginate. Measurements made with these materials revealed that enhancement of oxygen permeability of the encapsulating material with a concentrated PFC emulsion improves survival of encapsulated islets under hypoxic conditions, but reformulation of the PFC emulsion is needed to reduce toxicity.en_US
dc.description.sponsorshipNational Institutes of Health (U.S.) (Grant R01DK50657)en_US
dc.description.sponsorshipNational Institutes of Health (U.S.) (Grant R01-DK063108-01A1)en_US
dc.description.sponsorshipNational Institutes of Health (U.S.) (Grant NCRR ICR U42 16606)en_US
dc.description.sponsorshipJuvenile Diabetes Research Foundation Internationalen_US
dc.language.isoen_US
dc.publisherMary Ann Lieberten_US
dc.relation.isversionofhttp://dx.doi.org/10.1089/ten.tec.2009.0510en_US
dc.rightsArticle is made available in accordance with the publisher's policy and may be subject to US copyright law. Please refer to the publisher's site for terms of use.en_US
dc.sourceMary Ann Lieberten_US
dc.titleQuantitative Assessment of Islets of Langerhans Encapsulated in Alginateen_US
dc.typeArticleen_US
dc.identifier.citationJohnson, Amy S. et al. “Quantitative Assessment of Islets of Langerhans Encapsulated in Alginate.” Tissue Engineering Part C: Methods 17 (4) (2011): 435-449. Copyright © 2011, Mary Ann Liebert, Inc.en_US
dc.contributor.departmentMassachusetts Institute of Technology. Department of Chemical Engineeringen_US
dc.contributor.approverColton, Clark K.
dc.contributor.mitauthorJohnson, Amy S.
dc.contributor.mitauthorD'Aoust, Laura N.
dc.contributor.mitauthorFisher, Robert J.
dc.contributor.mitauthorColton, Clark K.
dc.relation.journalTissue Engineering. Part C, Methodsen_US
dc.eprint.versionFinal published versionen_US
dc.type.urihttp://purl.org/eprint/type/JournalArticleen_US
eprint.statushttp://purl.org/eprint/status/PeerRevieweden_US
dspace.orderedauthorsJohnson, Amy S.; O'Sullivan, Esther; D'Aoust, Laura N.; Omer, Abdulkadir; Bonner-Weir, Susan; Fisher, Robert J.; Weir, Gordon C.; Colton, Clark K.en
dc.identifier.orcidhttps://orcid.org/0000-0002-5834-5189
dc.identifier.orcidhttps://orcid.org/0000-0001-8777-9632
mit.licensePUBLISHER_POLICYen_US
mit.metadata.statusComplete


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