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   <subfield code="a">10.1007/s11095-011-0378-9</subfield>
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   <subfield code="a">(NATIONALLICENCE)springer-10.1007/s11095-011-0378-9</subfield>
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   <subfield code="a">Influence of Physical Properties of Biomaterials on Cellular Behavior</subfield>
   <subfield code="h">[Elektronische Daten]</subfield>
   <subfield code="c">[Susan Lin, Nivedita Sangaj, Tojo Razafiarison, Chao Zhang, Shyni Varghese]</subfield>
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   <subfield code="a">ABSTRACT: Purpose: In this study, we evaluated the effect of hydrogel structural properties on proliferation and biosynthesis activity of encapsulated chondrocytes. Methods: Hydrogels with varying structural and mechanical properties were prepared by photopolymerizing PEGDA precursors having MWs of 3.4kDa, 6kDa, 10kDa, and 20kDa and were characterized for their swelling ratio, network structure, morphology, and mechanical properties. The effect of hydrogel structural properties on the cellular activity of encapsulated chondrocytes was studied over four weeks. Results: Varying the molecular weight of PEGDA precursors exhibited a significant effect on the structural and mechanical properties of the hydrogels. Large mesh size was found to support cell proliferation. However, extracellular matrix (ECM) accumulation varied with the precursor molecular weight. Both PEGDA 6kDa and 10kDa hydrogels supported GAG accumulation, while PEGDA 10kDa and 20KDa hydrogels supported collagen accumulation. Chondrocytes cultured in PEGDA 10kDa hydrogels expressed a relative increase in collagen type II and aggrecan expression while maintaining low collagen type I expression. Conclusions: Increasing mesh size of the hydrogels resulted in an increase in cellular proliferation exhibiting the strong correlation between mesh size and cell growth, while mesh size had a differential effect on ECM accumulation and expression of cartilage specific markers.</subfield>
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   <subfield code="a">The Author(s), 2011</subfield>
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   <subfield code="a">cartilage</subfield>
   <subfield code="2">nationallicence</subfield>
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   <subfield code="a">chondrocytes</subfield>
   <subfield code="2">nationallicence</subfield>
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   <subfield code="a">GAG</subfield>
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   <subfield code="a">mesh size</subfield>
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   <subfield code="a">scaffold</subfield>
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   <subfield code="a">ECM : extracellular matrix</subfield>
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   <subfield code="a">PEG : poly(ethylene glycol)</subfield>
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   <subfield code="a">SR : swelling ratio</subfield>
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   <subfield code="a">$$ {\overline M_c} $$ : average molecular weight between two adjacent crosslinks</subfield>
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   <subfield code="a">ξ : mesh size</subfield>
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   <subfield code="a">Lin</subfield>
   <subfield code="D">Susan</subfield>
   <subfield code="u">Department of Bioengineering, University of California, San Diego, 9500 Gilman Drive, 92093-0412, La Jolla, California, USA</subfield>
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   <subfield code="a">Sangaj</subfield>
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   <subfield code="u">Department of Bioengineering, University of California, San Diego, 9500 Gilman Drive, 92093-0412, La Jolla, California, USA</subfield>
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   <subfield code="a">Zhang</subfield>
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