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Volume 6, Issue 9, Pages 3649-3656 (September 2010)


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Encapsulation of fibroblasts causes accelerated alginate hydrogel degradation

N.C. Hunta, A.M. Smitha, U. Gbureckb, R.M. Sheltonc, L.M. GroveraCorresponding Author Informationemail address

Received 10 December 2009; received in revised form 19 February 2010; accepted 17 March 2010. published online 22 March 2010.

Abstract 

Calcium-alginate hydrogel has been widely studied as a material for cell encapsulation for tissue engineering. At present, the effect that cells have on the degradation of alginate hydrogel is largely unknown. We have shown that fibroblasts encapsulated at a density of 7.5×105cellsml−1 in both 2% and 5% w/v alginate remain viable for at least 60days. Rheological analysis was used to study how the mechanical properties exhibited by alginate hydrogel changed during 28days in vitro culture. Alginate degradation was shown to occur throughout the study but was greatest within the first 7days of culture for all samples, which correlated with a sharp release of calcium ions from the construct. Fibroblasts were shown to increase the rate of degradation during the first 7days when compared with acellular samples in both 2% and 5% w/v gels, but after 28days both acellular and cell-encapsulating samples retained disc-shaped morphologies and gel-like spectra. The results demonstrate that although at an early stage cells influence the mechanical properties of encapsulating alginate, over a longer period of culture, the hydrogels retain sufficient mechanical integrity to exhibit gel-like properties. This allows sustained immobilization of the cells at the desired location in vivo where they can produce extracellular matrix and growth factors to expedite the healing process.

a School of Chemical Engineering, University of Birmingham, Birmingham B15 2TT, UK

b Department of Functional Materials in Medicine and Dentistry, University of Wurzburg, Wurzburg D97070, Germany

c School of Dentistry, University of Birmingham, Birmingham B4 6NN, UK

Corresponding Author InformationCorresponding author. Tel.: +44 121 414 3887; fax: +44 121 414 5324.

PII: S1742-7061(10)00152-2

doi:10.1016/j.actbio.2010.03.026


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