Document Detail


Enhancing oxygen tension and cellular function in alginate cell encapsulation devices through the use of perfluorocarbons.
MedLine Citation:
PMID:  16917927     Owner:  NLM     Status:  MEDLINE    
Abstract/OtherAbstract:
Encapsulation devices are often hindered by the inability to achieve sufficient oxygen levels for sustaining long-term cell survival both in vivo and in vitro. We have investigated the use of synthetic oxygen carriers in alginate gels to improve metabolic activity and viability of HepG2 cells over time. Perfluorocarbons (PFCs), specifically perfluorotributylamine (PFTBA) and perfluorooctylbromide (PFOB), were emulsified with alginate and used to encapsulate HepG2 cells in a spherical geometry. Cellular state was assessed using the MTT assay and Live/Dead stain as well as through analysis of both lactate and lactate dehydrogenase (LDH) levels which are indirect indicators of oxygen availability. Addition of 1% surfactant resulted in stable emulsions with evenly dispersed PFC droplets of the order of 1-2 microm in diameter, with no influence on cell viability. Both PFCs evaluated were effective in increasing cellular metabolic activity over alginate-only gels. The presence of 10% PFOB significantly increased cellular growth rate by 10% and reduced both intracellular LDH and extracellular lactate levels by 20-40%, improving glucose utilization efficiency. The characteristic drop in cellular metabolic activity upon encapsulation was eliminated with addition of 10% PFC and viability was better maintained throughout the bead, with a significant decrease in necrotic core size. Results were consistent under a physiologically relevant 5% oxygen environment. The incorporation of PFC synthetic oxygen carriers into encapsulation matrices has been successfully applied to improve cell function and viability with implication for a variety of tissue engineering applications.
Authors:
Sarwat F Khattak; Kyuong-sik Chin; Surita R Bhatia; Susan C Roberts
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Publication Detail:
Type:  Journal Article; Research Support, N.I.H., Extramural; Research Support, Non-U.S. Gov't; Research Support, U.S. Gov't, Non-P.H.S.    
Journal Detail:
Title:  Biotechnology and bioengineering     Volume:  96     ISSN:  0006-3592     ISO Abbreviation:  Biotechnol. Bioeng.     Publication Date:  2007 Jan 
Date Detail:
Created Date:  2006-12-05     Completed Date:  2007-02-28     Revised Date:  2007-12-03    
Medline Journal Info:
Nlm Unique ID:  7502021     Medline TA:  Biotechnol Bioeng     Country:  United States    
Other Details:
Languages:  eng     Pagination:  156-66     Citation Subset:  IM    
Affiliation:
Department of Chemical Engineering, University of Massachusetts, Amherst, MA 01003, USA.
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MeSH Terms
Descriptor/Qualifier:
Alginates / chemistry*
Cell Culture Techniques / methods*
Cell Line
Cell Proliferation
Cell Survival
Coated Materials, Biocompatible / chemistry
Fluorocarbons / chemistry*
Glucuronic Acid / chemistry
Hepatocytes / cytology*,  physiology*
Hexuronic Acids / chemistry
Humans
Materials Testing
Oxygen / metabolism*
Tissue Engineering / methods*
Grant Support
ID/Acronym/Agency:
T32 GM08515/GM/NIGMS NIH HHS
Chemical
Reg. No./Substance:
0/Alginates; 0/Coated Materials, Biocompatible; 0/Fluorocarbons; 0/Hexuronic Acids; 576-37-4/Glucuronic Acid; 7782-44-7/Oxygen; 9005-32-7/alginic acid

From MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine


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