Source:http://linkedlifedata.com/resource/pubmed/id/21306293
Switch to
Predicate | Object |
---|---|
rdf:type | |
lifeskim:mentions | |
pubmed:issue |
13-14
|
pubmed:dateCreated |
2011-6-24
|
pubmed:abstractText |
Poly(ethylene glycol) (PEG) hydrogels are popular for cell culture and tissue-engineering applications because they are nontoxic and exhibit favorable hydration and nutrient transport properties. However, cells cannot adhere to, remodel, proliferate within, or degrade PEG hydrogels. Methacrylated gelatin (GelMA), derived from denatured collagen, yields an enzymatically degradable, photocrosslinkable hydrogel that cells can degrade, adhere to and spread within. To combine the desirable features of each of these materials we synthesized PEG-GelMA composite hydrogels, hypothesizing that copolymerization would enable adjustable cell binding, mechanical, and degradation properties. The addition of GelMA to PEG resulted in a composite hydrogel that exhibited tunable mechanical and biological profiles. Adding GelMA (5%-15% w/v) to PEG (5% and 10% w/v) proportionally increased fibroblast surface binding and spreading as compared to PEG hydrogels (p<0.05). Encapsulated fibroblasts were also able to form 3D cellular networks 7 days after photoencapsulation only within composite hydrogels as compared to PEG alone. Additionally, PEG-GelMA hydrogels displayed tunable enzymatic degradation and stiffness profiles. PEG-GelMA composite hydrogels show great promise as tunable, cell-responsive hydrogels for 3D cell culture and regenerative medicine applications.
|
pubmed:grant |
http://linkedlifedata.com/resource/pubmed/grant/AR057837,
http://linkedlifedata.com/resource/pubmed/grant/DE019024,
http://linkedlifedata.com/resource/pubmed/grant/EB012597,
http://linkedlifedata.com/resource/pubmed/grant/HL092836,
http://linkedlifedata.com/resource/pubmed/grant/HL099073,
http://linkedlifedata.com/resource/pubmed/grant/R01 HL092836-02S1,
http://linkedlifedata.com/resource/pubmed/grant/R01 HL092836-04,
http://linkedlifedata.com/resource/pubmed/grant/RL1 DE019024-04,
http://linkedlifedata.com/resource/pubmed/grant/RL1 DE019024-05
|
pubmed:language |
eng
|
pubmed:journal | |
pubmed:citationSubset |
IM
|
pubmed:chemical |
http://linkedlifedata.com/resource/pubmed/chemical/Gelatin,
http://linkedlifedata.com/resource/pubmed/chemical/Hydrogels,
http://linkedlifedata.com/resource/pubmed/chemical/Methacrylates,
http://linkedlifedata.com/resource/pubmed/chemical/Polyethylene Glycols,
http://linkedlifedata.com/resource/pubmed/chemical/Water
|
pubmed:status |
MEDLINE
|
pubmed:month |
Jul
|
pubmed:issn |
1937-335X
|
pubmed:author | |
pubmed:issnType |
Electronic
|
pubmed:volume |
17
|
pubmed:owner |
NLM
|
pubmed:authorsComplete |
Y
|
pubmed:pagination |
1713-23
|
pubmed:meshHeading |
pubmed-meshheading:21306293-Animals,
pubmed-meshheading:21306293-Cell Adhesion,
pubmed-meshheading:21306293-Cell Survival,
pubmed-meshheading:21306293-Fibroblasts,
pubmed-meshheading:21306293-Gelatin,
pubmed-meshheading:21306293-Hydrogels,
pubmed-meshheading:21306293-Mechanical Phenomena,
pubmed-meshheading:21306293-Methacrylates,
pubmed-meshheading:21306293-Mice,
pubmed-meshheading:21306293-NIH 3T3 Cells,
pubmed-meshheading:21306293-Polyethylene Glycols,
pubmed-meshheading:21306293-Surface Properties,
pubmed-meshheading:21306293-Water
|
pubmed:year |
2011
|
pubmed:articleTitle |
Synthesis and characterization of tunable poly(ethylene glycol): gelatin methacrylate composite hydrogels.
|
pubmed:affiliation |
Department of Medicine, Center for Biomedical Engineering, Brigham and Women's Hospital, Harvard Medical School, Cambridge, Massachusetts 02139, USA.
|
pubmed:publicationType |
Journal Article,
Research Support, U.S. Gov't, Non-P.H.S.,
Research Support, N.I.H., Extramural
|