In situ cross-linkable gelatin–poly(ethylene glycol)–tyramine hydrogel via enzyme-mediated reaction for tissue regenerative medicine
An in situ cross-linkable gelatin-poly(ethylene glycol)-tyramine (GPT) hydrogel was developed as a novel injectable material for tissue regenerative medicine. The hydrogel was formed rapidly using horseradish peroxidase (HRP) and hydrogen peroxide (H2O2). The gelation times could be controlled from...
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Veröffentlicht in: | Journal of materials chemistry 2011-01, Vol.21 (35), p.13180-13187 |
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container_title | Journal of materials chemistry |
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creator | Park, Kyung Min Ko, Ki Seong Joung, Yoon Ki Shin, Heungsoo Park, Ki Dong |
description | An in situ cross-linkable gelatin-poly(ethylene glycol)-tyramine (GPT) hydrogel was developed as a novel injectable material for tissue regenerative medicine. The hydrogel was formed rapidly using horseradish peroxidase (HRP) and hydrogen peroxide (H2O2). The gelation times could be controlled from five seconds to over one minute by changing the HRP concentration, and the mechanical properties could be controlled by varying the H2O2 concentration. The storage moduli of the hydrogels ranged from approximately 200 to over 8000 Pa. In addition, an in vitro cell attachment study was carried out using various cell types. The results of this study demonstrated that the GPT hydrogel, formed in situ via an enzyme-mediated reaction, was an excellent bioactive matrix for cellular behavior. Furthermore, an in vitro 3D cell study was made using the GPT hydrogels formed with different mechanical strengths, and in vivo subcutaneous injection was carried out. The in vitro and in vivo studies demonstrated that the GPT hydrogels had excellent bioactivities, and that the cellular behavior in the hydrogel matrix could be controlled. The obtained results showed that these in situ forming GPT hydrogels, with excellent bioactivities and tunable physicochemical properties, have great potential for use as injectable materials in tissue regenerative medicine and various biomedical applications. |
doi_str_mv | 10.1039/c1jm12527c |
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The hydrogel was formed rapidly using horseradish peroxidase (HRP) and hydrogen peroxide (H2O2). The gelation times could be controlled from five seconds to over one minute by changing the HRP concentration, and the mechanical properties could be controlled by varying the H2O2 concentration. The storage moduli of the hydrogels ranged from approximately 200 to over 8000 Pa. In addition, an in vitro cell attachment study was carried out using various cell types. The results of this study demonstrated that the GPT hydrogel, formed in situ via an enzyme-mediated reaction, was an excellent bioactive matrix for cellular behavior. Furthermore, an in vitro 3D cell study was made using the GPT hydrogels formed with different mechanical strengths, and in vivo subcutaneous injection was carried out. The in vitro and in vivo studies demonstrated that the GPT hydrogels had excellent bioactivities, and that the cellular behavior in the hydrogel matrix could be controlled. The obtained results showed that these in situ forming GPT hydrogels, with excellent bioactivities and tunable physicochemical properties, have great potential for use as injectable materials in tissue regenerative medicine and various biomedical applications.</description><identifier>ISSN: 0959-9428</identifier><identifier>EISSN: 1364-5501</identifier><identifier>DOI: 10.1039/c1jm12527c</identifier><language>eng</language><subject>Biocompatibility ; Biomedical materials ; Cellular ; Hydrogels ; In vitro testing ; Medicine ; Regenerative ; Surgical implants</subject><ispartof>Journal of materials chemistry, 2011-01, Vol.21 (35), p.13180-13187</ispartof><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c329t-35c71a3e49ed89e226aa91583e4185c1ee7f3b5f303ced9da6badce16d68e1323</citedby><cites>FETCH-LOGICAL-c329t-35c71a3e49ed89e226aa91583e4185c1ee7f3b5f303ced9da6badce16d68e1323</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,776,780,27901,27902</link.rule.ids></links><search><creatorcontrib>Park, Kyung Min</creatorcontrib><creatorcontrib>Ko, Ki Seong</creatorcontrib><creatorcontrib>Joung, Yoon Ki</creatorcontrib><creatorcontrib>Shin, Heungsoo</creatorcontrib><creatorcontrib>Park, Ki Dong</creatorcontrib><title>In situ cross-linkable gelatin–poly(ethylene glycol)–tyramine hydrogel via enzyme-mediated reaction for tissue regenerative medicine</title><title>Journal of materials chemistry</title><description>An in situ cross-linkable gelatin-poly(ethylene glycol)-tyramine (GPT) hydrogel was developed as a novel injectable material for tissue regenerative medicine. The hydrogel was formed rapidly using horseradish peroxidase (HRP) and hydrogen peroxide (H2O2). The gelation times could be controlled from five seconds to over one minute by changing the HRP concentration, and the mechanical properties could be controlled by varying the H2O2 concentration. The storage moduli of the hydrogels ranged from approximately 200 to over 8000 Pa. In addition, an in vitro cell attachment study was carried out using various cell types. The results of this study demonstrated that the GPT hydrogel, formed in situ via an enzyme-mediated reaction, was an excellent bioactive matrix for cellular behavior. Furthermore, an in vitro 3D cell study was made using the GPT hydrogels formed with different mechanical strengths, and in vivo subcutaneous injection was carried out. The in vitro and in vivo studies demonstrated that the GPT hydrogels had excellent bioactivities, and that the cellular behavior in the hydrogel matrix could be controlled. The obtained results showed that these in situ forming GPT hydrogels, with excellent bioactivities and tunable physicochemical properties, have great potential for use as injectable materials in tissue regenerative medicine and various biomedical applications.</description><subject>Biocompatibility</subject><subject>Biomedical materials</subject><subject>Cellular</subject><subject>Hydrogels</subject><subject>In vitro testing</subject><subject>Medicine</subject><subject>Regenerative</subject><subject>Surgical implants</subject><issn>0959-9428</issn><issn>1364-5501</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2011</creationdate><recordtype>article</recordtype><recordid>eNpFkLtOwzAYRi0EEqWw8ATeuEgBX-okHlHFpVIlFpgj1_nTujhxsZ1KYWJk5w15ElxAYvqko6MzfAidUnJFCZfXmq5bygQr9B4aUZ5PMiEI3UcjIoXM5ISVh-gohDUhlBa5GKGPWYeDiT3W3oWQWdO9qIUFvASroum-3j83zg7nEFeDhS5xO2hnLxKPg1etSWg11N4lH2-NwtC9DS1kLdRGRaixB6WjcR1unMfRhNBDYsuU8qm_Bbwzdcoco4NG2QAnfztGz3e3T9OHbP54P5vezDPNmYwZF7qgisNEQl1KYCxXSlJRJkJLoSlA0fCFaDjhGmpZq3yhag00r_MSKGd8jM5-uxvvXnsIsWpN0GCt6sD1oZI5LwWbFCSZl7_mzzUemmrjTav8UFFS7d6u_t_m38HYeRQ</recordid><startdate>20110101</startdate><enddate>20110101</enddate><creator>Park, Kyung Min</creator><creator>Ko, Ki Seong</creator><creator>Joung, Yoon Ki</creator><creator>Shin, Heungsoo</creator><creator>Park, Ki Dong</creator><scope>AAYXX</scope><scope>CITATION</scope><scope>7SR</scope><scope>7U5</scope><scope>8BQ</scope><scope>8FD</scope><scope>JG9</scope><scope>L7M</scope></search><sort><creationdate>20110101</creationdate><title>In situ cross-linkable gelatin–poly(ethylene glycol)–tyramine hydrogel via enzyme-mediated reaction for tissue regenerative medicine</title><author>Park, Kyung Min ; Ko, Ki Seong ; Joung, Yoon Ki ; Shin, Heungsoo ; Park, Ki Dong</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c329t-35c71a3e49ed89e226aa91583e4185c1ee7f3b5f303ced9da6badce16d68e1323</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2011</creationdate><topic>Biocompatibility</topic><topic>Biomedical materials</topic><topic>Cellular</topic><topic>Hydrogels</topic><topic>In vitro testing</topic><topic>Medicine</topic><topic>Regenerative</topic><topic>Surgical implants</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Park, Kyung Min</creatorcontrib><creatorcontrib>Ko, Ki Seong</creatorcontrib><creatorcontrib>Joung, Yoon Ki</creatorcontrib><creatorcontrib>Shin, Heungsoo</creatorcontrib><creatorcontrib>Park, Ki Dong</creatorcontrib><collection>CrossRef</collection><collection>Engineered Materials Abstracts</collection><collection>Solid State and Superconductivity Abstracts</collection><collection>METADEX</collection><collection>Technology Research Database</collection><collection>Materials Research Database</collection><collection>Advanced Technologies Database with Aerospace</collection><jtitle>Journal of materials chemistry</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Park, Kyung Min</au><au>Ko, Ki Seong</au><au>Joung, Yoon Ki</au><au>Shin, Heungsoo</au><au>Park, Ki Dong</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>In situ cross-linkable gelatin–poly(ethylene glycol)–tyramine hydrogel via enzyme-mediated reaction for tissue regenerative medicine</atitle><jtitle>Journal of materials chemistry</jtitle><date>2011-01-01</date><risdate>2011</risdate><volume>21</volume><issue>35</issue><spage>13180</spage><epage>13187</epage><pages>13180-13187</pages><issn>0959-9428</issn><eissn>1364-5501</eissn><abstract>An in situ cross-linkable gelatin-poly(ethylene glycol)-tyramine (GPT) hydrogel was developed as a novel injectable material for tissue regenerative medicine. The hydrogel was formed rapidly using horseradish peroxidase (HRP) and hydrogen peroxide (H2O2). The gelation times could be controlled from five seconds to over one minute by changing the HRP concentration, and the mechanical properties could be controlled by varying the H2O2 concentration. The storage moduli of the hydrogels ranged from approximately 200 to over 8000 Pa. In addition, an in vitro cell attachment study was carried out using various cell types. The results of this study demonstrated that the GPT hydrogel, formed in situ via an enzyme-mediated reaction, was an excellent bioactive matrix for cellular behavior. Furthermore, an in vitro 3D cell study was made using the GPT hydrogels formed with different mechanical strengths, and in vivo subcutaneous injection was carried out. The in vitro and in vivo studies demonstrated that the GPT hydrogels had excellent bioactivities, and that the cellular behavior in the hydrogel matrix could be controlled. The obtained results showed that these in situ forming GPT hydrogels, with excellent bioactivities and tunable physicochemical properties, have great potential for use as injectable materials in tissue regenerative medicine and various biomedical applications.</abstract><doi>10.1039/c1jm12527c</doi><tpages>8</tpages></addata></record> |
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source | Royal Society Of Chemistry Journals 2008-; Alma/SFX Local Collection |
subjects | Biocompatibility Biomedical materials Cellular Hydrogels In vitro testing Medicine Regenerative Surgical implants |
title | In situ cross-linkable gelatin–poly(ethylene glycol)–tyramine hydrogel via enzyme-mediated reaction for tissue regenerative medicine |
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