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Evaluation of physical and mechanical properties of porous poly (ethylene glycol)-co-(L-lactic acid) hydrogels during degradation
Porous hydrogels of poly(ethylene glycol) (PEG) have been shown to facilitate vascularized tissue formation. However, PEG hydrogels exhibit limited degradation under physiological conditions which hinders their ultimate applicability for tissue engineering therapies. Introduction of poly(L-lactic ac...
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Published in: | PloS one 2013-04, Vol.8 (4), p.e60728-e60728 |
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description | Porous hydrogels of poly(ethylene glycol) (PEG) have been shown to facilitate vascularized tissue formation. However, PEG hydrogels exhibit limited degradation under physiological conditions which hinders their ultimate applicability for tissue engineering therapies. Introduction of poly(L-lactic acid) (PLLA) chains into the PEG backbone results in copolymers that exhibit degradation via hydrolysis that can be controlled, in part, by the copolymer conditions. In this study, porous, PEG-PLLA hydrogels were generated by solvent casting/particulate leaching and photopolymerization. The influence of polymer conditions on hydrogel architecture, degradation and mechanical properties was investigated. Autofluorescence exhibited by the hydrogels allowed for three-dimensional, non-destructive monitoring of hydrogel structure under fully swelled conditions. The initial pore size depended on particulate size but not polymer concentration, while degradation time was dependent on polymer concentration. Compressive modulus was a function of polymer concentration and decreased as the hydrogels degraded. Interestingly, pore size did not vary during degradation contrary to what has been observed in other polymer systems. These results provide a technique for generating porous, degradable PEG-PLLA hydrogels and insight into how the degradation, structure, and mechanical properties depend on synthesis conditions. |
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However, PEG hydrogels exhibit limited degradation under physiological conditions which hinders their ultimate applicability for tissue engineering therapies. Introduction of poly(L-lactic acid) (PLLA) chains into the PEG backbone results in copolymers that exhibit degradation via hydrolysis that can be controlled, in part, by the copolymer conditions. In this study, porous, PEG-PLLA hydrogels were generated by solvent casting/particulate leaching and photopolymerization. The influence of polymer conditions on hydrogel architecture, degradation and mechanical properties was investigated. Autofluorescence exhibited by the hydrogels allowed for three-dimensional, non-destructive monitoring of hydrogel structure under fully swelled conditions. The initial pore size depended on particulate size but not polymer concentration, while degradation time was dependent on polymer concentration. Compressive modulus was a function of polymer concentration and decreased as the hydrogels degraded. Interestingly, pore size did not vary during degradation contrary to what has been observed in other polymer systems. These results provide a technique for generating porous, degradable PEG-PLLA hydrogels and insight into how the degradation, structure, and mechanical properties depend on synthesis conditions.</description><identifier>ISSN: 1932-6203</identifier><identifier>EISSN: 1932-6203</identifier><identifier>DOI: 10.1371/journal.pone.0060728</identifier><identifier>PMID: 23593296</identifier><language>eng</language><publisher>United States: Public Library of Science</publisher><subject>Acids ; Animals ; Biocompatible Materials ; Biology ; Biomechanical Phenomena ; Biomedical engineering ; Biomedical materials ; Cell Line ; Chemistry ; Degradation ; Engineering ; Fibroblasts - metabolism ; Focal Adhesions ; Hydrogels ; Hydrogels - chemistry ; Influence ; Leaching ; Materials Science ; Mechanical properties ; Mice ; Modulus of elasticity ; Particle Size ; Particulate size ; Particulates ; Photopolymerization ; Physical chemistry ; Polyethylene glycol ; Polyethylene Glycols - chemistry ; Polylactic acid ; Polymerization ; Polymers ; Pore size ; Porosity ; Tissue engineering</subject><ispartof>PloS one, 2013-04, Vol.8 (4), p.e60728-e60728</ispartof><rights>2013 Chiu et al. This is an open-access article distributed under the terms of the Creative Commons Attribution License: https://creativecommons.org/licenses/by/4.0/ (the “License”), which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.</rights><rights>2013 Chiu et al 2013 Chiu et al</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c526t-db54ae6aeb6812565e7069b2b0390b16240a00744ebb3e484203c35c01a8f2723</citedby><cites>FETCH-LOGICAL-c526t-db54ae6aeb6812565e7069b2b0390b16240a00744ebb3e484203c35c01a8f2723</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.proquest.com/docview/1330895106/fulltextPDF?pq-origsite=primo$$EPDF$$P50$$Gproquest$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.proquest.com/docview/1330895106?pq-origsite=primo$$EHTML$$P50$$Gproquest$$Hfree_for_read</linktohtml><link.rule.ids>230,315,733,786,790,891,25783,27957,27958,37047,37048,44625,53827,53829,75483</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/23593296$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><contributor>Barbosa, Mário A.</contributor><creatorcontrib>Chiu, Yu-Chieh</creatorcontrib><creatorcontrib>Kocagöz, Sevi</creatorcontrib><creatorcontrib>Larson, Jeffery C</creatorcontrib><creatorcontrib>Brey, Eric M</creatorcontrib><title>Evaluation of physical and mechanical properties of porous poly (ethylene glycol)-co-(L-lactic acid) hydrogels during degradation</title><title>PloS one</title><addtitle>PLoS One</addtitle><description>Porous hydrogels of poly(ethylene glycol) (PEG) have been shown to facilitate vascularized tissue formation. However, PEG hydrogels exhibit limited degradation under physiological conditions which hinders their ultimate applicability for tissue engineering therapies. Introduction of poly(L-lactic acid) (PLLA) chains into the PEG backbone results in copolymers that exhibit degradation via hydrolysis that can be controlled, in part, by the copolymer conditions. In this study, porous, PEG-PLLA hydrogels were generated by solvent casting/particulate leaching and photopolymerization. The influence of polymer conditions on hydrogel architecture, degradation and mechanical properties was investigated. Autofluorescence exhibited by the hydrogels allowed for three-dimensional, non-destructive monitoring of hydrogel structure under fully swelled conditions. The initial pore size depended on particulate size but not polymer concentration, while degradation time was dependent on polymer concentration. Compressive modulus was a function of polymer concentration and decreased as the hydrogels degraded. Interestingly, pore size did not vary during degradation contrary to what has been observed in other polymer systems. These results provide a technique for generating porous, degradable PEG-PLLA hydrogels and insight into how the degradation, structure, and mechanical properties depend on synthesis conditions.</description><subject>Acids</subject><subject>Animals</subject><subject>Biocompatible Materials</subject><subject>Biology</subject><subject>Biomechanical Phenomena</subject><subject>Biomedical engineering</subject><subject>Biomedical materials</subject><subject>Cell Line</subject><subject>Chemistry</subject><subject>Degradation</subject><subject>Engineering</subject><subject>Fibroblasts - metabolism</subject><subject>Focal Adhesions</subject><subject>Hydrogels</subject><subject>Hydrogels - chemistry</subject><subject>Influence</subject><subject>Leaching</subject><subject>Materials Science</subject><subject>Mechanical properties</subject><subject>Mice</subject><subject>Modulus of elasticity</subject><subject>Particle Size</subject><subject>Particulate size</subject><subject>Particulates</subject><subject>Photopolymerization</subject><subject>Physical chemistry</subject><subject>Polyethylene glycol</subject><subject>Polyethylene Glycols - 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Academic</collection><collection>PubMed Central (Full Participant titles)</collection><collection>DOAJ Directory of Open Access Journals</collection><jtitle>PloS one</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Chiu, Yu-Chieh</au><au>Kocagöz, Sevi</au><au>Larson, Jeffery C</au><au>Brey, Eric M</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Evaluation of physical and mechanical properties of porous poly (ethylene glycol)-co-(L-lactic acid) hydrogels during degradation</atitle><jtitle>PloS one</jtitle><addtitle>PLoS One</addtitle><date>2013-04-09</date><risdate>2013</risdate><volume>8</volume><issue>4</issue><spage>e60728</spage><epage>e60728</epage><pages>e60728-e60728</pages><issn>1932-6203</issn><eissn>1932-6203</eissn><notes>ObjectType-Article-1</notes><notes>SourceType-Scholarly Journals-1</notes><notes>ObjectType-Feature-2</notes><notes>content type line 23</notes><notes>Competing Interests: The authors have declared that no competing interests exist.</notes><notes>Conceived and designed the experiments: YCC SK EMB. Performed the experiments: YCC SK JCL. Analyzed the data: YCC SK JCL EMB. Wrote the paper: YCC SK JCL EMB.</notes><abstract>Porous hydrogels of poly(ethylene glycol) (PEG) have been shown to facilitate vascularized tissue formation. However, PEG hydrogels exhibit limited degradation under physiological conditions which hinders their ultimate applicability for tissue engineering therapies. Introduction of poly(L-lactic acid) (PLLA) chains into the PEG backbone results in copolymers that exhibit degradation via hydrolysis that can be controlled, in part, by the copolymer conditions. In this study, porous, PEG-PLLA hydrogels were generated by solvent casting/particulate leaching and photopolymerization. The influence of polymer conditions on hydrogel architecture, degradation and mechanical properties was investigated. Autofluorescence exhibited by the hydrogels allowed for three-dimensional, non-destructive monitoring of hydrogel structure under fully swelled conditions. The initial pore size depended on particulate size but not polymer concentration, while degradation time was dependent on polymer concentration. Compressive modulus was a function of polymer concentration and decreased as the hydrogels degraded. Interestingly, pore size did not vary during degradation contrary to what has been observed in other polymer systems. These results provide a technique for generating porous, degradable PEG-PLLA hydrogels and insight into how the degradation, structure, and mechanical properties depend on synthesis conditions.</abstract><cop>United States</cop><pub>Public Library of Science</pub><pmid>23593296</pmid><doi>10.1371/journal.pone.0060728</doi><oa>free_for_read</oa></addata></record> |
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subjects | Acids Animals Biocompatible Materials Biology Biomechanical Phenomena Biomedical engineering Biomedical materials Cell Line Chemistry Degradation Engineering Fibroblasts - metabolism Focal Adhesions Hydrogels Hydrogels - chemistry Influence Leaching Materials Science Mechanical properties Mice Modulus of elasticity Particle Size Particulate size Particulates Photopolymerization Physical chemistry Polyethylene glycol Polyethylene Glycols - chemistry Polylactic acid Polymerization Polymers Pore size Porosity Tissue engineering |
title | Evaluation of physical and mechanical properties of porous poly (ethylene glycol)-co-(L-lactic acid) hydrogels during degradation |
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