Mammalian cell survival and processing in supercritical CO sub(2)
We demonstrate that mammalian cells can survive for 5 min within high-pressure CO sub(2) sub(.) Cell survival was investigated by exposing a range of mammalian cell types to supercritical CO sub(2) (scCO sub(2)) (35 degree C, 74 bar; 1 bar = 100 kPa) for increasing exposure and depressurization time...
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Published in | Proceedings of the National Academy of Sciences - PNAS Vol. 103; no. 19; pp. 7426 - 7431 |
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Main Authors | , , , , , , , , , , |
Format | Journal Article |
Language | English |
Published |
09.05.2006
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Online Access | Get full text |
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Summary: | We demonstrate that mammalian cells can survive for 5 min within high-pressure CO sub(2) sub(.) Cell survival was investigated by exposing a range of mammalian cell types to supercritical CO sub(2) (scCO sub(2)) (35 degree C, 74 bar; 1 bar = 100 kPa) for increasing exposure and depressurization times. The myoblastic C2C12 cell line, 3T3 fibroblasts, chondrocytes, and hepatocytes all displayed appreciable but varying metabolic activity with exposure times up to 1 min. With depressurization times of 4 min, cell population metabolic activity was greater than or equal to 70% of the control population. Based on survival data, we developed a single-step scCO sub(2) technique for the rapid production of biodegradable poly(DL-lactic acid) scaffolds containing mammalian cells. By using optimum cell-survival conditions, scCO sub(2) was used to process poly(DL-lactic acid) containing a cell suspension, and, upon pressure release, a polymer sponge containing viable mammalian cells was formed. Cell functionality was demonstrated by retention of an osteogenic response to bone morphogenetic protein-2 in C2C12 cells. A gene microarray analysis showed no statistically significant changes in gene expression across 4,418 genes by a single-class t test. A significance analysis of microarrays revealed only eight genes that were down-regulated based on a delta value of 1.0125 and a false detection rate of 0. |
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Bibliography: | ObjectType-Article-2 SourceType-Scholarly Journals-1 content type line 23 ObjectType-Feature-1 |
ISSN: | 0027-8424 1091-6490 |