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Thermally reversible colloidal gels for three-dimensional chondrocyte culture
Author(s) -
James W. Lapworth,
Paul V. Hatton,
Rebecca L. Goodchild,
Stephen Rimmer
Publication year - 2011
Publication title -
journal of the royal society interface
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.655
H-Index - 139
eISSN - 1742-5689
pISSN - 1742-5662
DOI - 10.1098/rsif.2011.0308
Subject(s) - chondrocyte , copolymer , polymer , styrene , glycosaminoglycan , lower critical solution temperature , colloid , biophysics , chemistry , swelling , chemical engineering , cell culture , tissue engineering , polymer chemistry , materials science , in vitro , biomedical engineering , biochemistry , organic chemistry , biology , composite material , engineering , medicine , genetics
Healthy cells are required in large numbers to form a tissue-engineered construct and primary cells must therefore be increased in number in a process termed 'expansion'. There are significant problems with existing procedures, including cell injury and an associated loss of phenotype, but three-dimensional culture has been reported to offer a solution. Reversible gels, which allow for the recovery of cells after expansion would therefore have great value in the expansion of chondrocytes for tissue engineering applications, but they have received relatively little attention to date. In this study, we examined the synthesis and use of thermoresponsive polymers that form reversible three-dimensional gels for chondrocyte cell culture. A series of polymers comprising N-isopropylacrylamide (NIPAM) and styrene was synthesized before studying their thermoresponsive solution behaviour and gelation. A poly(NIPAM-co-styrene-graft-N-vinylpyrrolidone) variant was also synthesized in order to provide increased water content. Both random- and graft-copolymers formed particulate gels above the lower critical solution temperature and, on cooling, re-dissolved to allow enzyme-free cell recovery. Chondrocytes remained viable in all of these materials for 24 days, increased in number and produced collagen type II and glycosaminoglycans.

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