Preparation of TGF-β1-conjugated biodegradable pluronic F127 hydrogel and its application with adipose-derived stem cells
In this study, a composite hydrogel using Pluronic F127 derivatives and crosslinked hyaluronic acid (X-HA) was investigated, exploring the benefits in the induction of chondrogenic differentiation of human adipose-derived stem cells (ASCs). F127 was chemically modified through a series of reactions...
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description | In this study, a composite hydrogel using Pluronic F127 derivatives and crosslinked hyaluronic acid (X-HA) was investigated, exploring the benefits in the induction of chondrogenic differentiation of human adipose-derived stem cells (ASCs). F127 was chemically modified through a series of reactions that produced multiple F127 derivatives. A chondrogenic growth factor, transforming growth factor-beta 1 (TGF-β1) was then coupled to the heparin-conjugated F127. X-HA was used as a physical stabilizer of the composite hydrogel (X-HA/F127). The chemical structures of F127 derivatives were analyzed using
1H-NMR and ATR-FTIR. Sol–gel transition of the composite hydrogel was identified at body temperature. The conjugated TGF-β1 was moderately released
in vitro from the composite hydrogel. Cell viability of human ASCs in the hydrogels was about 50% after
in vitro culture for 3
days. As the ASCs/hydrogel were injected into nude mice subcutaneously, DAPI staining of the retrieved constructs showed that ASCs were dispersed through the hydrogel matrix. From the immunofluorescent staining of type II collagen, the TGF-conjugated group exhibited more active green signals than the others. In addition, when those constructs were loaded into the full-thickness defect of rabbit knee articular cartilage, Alcian blue staining identified the formation of cartilaginous matrix from the TGF-conjugated hydrogel. The present work indicated that X-HA/F127 composite hydrogel was thermoreversible and biodegradable, and that the TGF-conjugated hydrogel could be effective in inducing chondrogenesis of human ASCs.
[Display omitted] |
doi_str_mv | 10.1016/j.jconrel.2010.06.020 |
format | Article |
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1H-NMR and ATR-FTIR. Sol–gel transition of the composite hydrogel was identified at body temperature. The conjugated TGF-β1 was moderately released
in vitro from the composite hydrogel. Cell viability of human ASCs in the hydrogels was about 50% after
in vitro culture for 3
days. As the ASCs/hydrogel were injected into nude mice subcutaneously, DAPI staining of the retrieved constructs showed that ASCs were dispersed through the hydrogel matrix. From the immunofluorescent staining of type II collagen, the TGF-conjugated group exhibited more active green signals than the others. In addition, when those constructs were loaded into the full-thickness defect of rabbit knee articular cartilage, Alcian blue staining identified the formation of cartilaginous matrix from the TGF-conjugated hydrogel. The present work indicated that X-HA/F127 composite hydrogel was thermoreversible and biodegradable, and that the TGF-conjugated hydrogel could be effective in inducing chondrogenesis of human ASCs.
[Display omitted]</description><identifier>ISSN: 0168-3659</identifier><identifier>EISSN: 1873-4995</identifier><identifier>DOI: 10.1016/j.jconrel.2010.06.020</identifier><identifier>PMID: 20599451</identifier><identifier>CODEN: JCREEC</identifier><language>eng</language><publisher>Kidlington: Elsevier B.V</publisher><subject>Absorbable Implants ; Adipose Tissue - cytology ; Adipose Tissue - drug effects ; Animals ; Biocompatible Materials - chemistry ; Biological and medical sciences ; Cartilage, Articular - drug effects ; Cell Culture Techniques ; Cell Differentiation - drug effects ; Chondrogenesis ; Conjugation ; Disease Models, Animal ; Drug Carriers - chemistry ; General pharmacology ; Human adipose-derived stem cell ; Humans ; Hydrogels ; Medical sciences ; Mice ; Mice, Nude ; Osteochondritis - therapy ; Pharmaceutical technology. Pharmaceutical industry ; Pharmacology. Drug treatments ; Pluronic F127 ; Poloxamer - chemistry ; Rabbits ; Stem Cells - cytology ; Stem Cells - drug effects ; Stem Cells - metabolism ; TGF-β1 release ; Tissue Engineering ; Tissue Scaffolds - chemistry ; Transforming Growth Factor beta1 - administration & dosage ; Transforming Growth Factor beta1 - pharmacology ; Transforming Growth Factor beta1 - therapeutic use</subject><ispartof>Journal of controlled release, 2010-10, Vol.147 (1), p.84-91</ispartof><rights>2010 Elsevier B.V.</rights><rights>2015 INIST-CNRS</rights><rights>Copyright © 2010 Elsevier B.V. All rights reserved.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c309t-ed67223e7507baea40ea0d470095e7228f2a23dd40235a1b918680a379b6277e3</citedby></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://dx.doi.org/10.1016/j.jconrel.2010.06.020$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>314,780,784,3550,27924,27925,45995</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=23288008$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/20599451$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Jung, Hong Hee</creatorcontrib><creatorcontrib>Park, Kwideok</creatorcontrib><creatorcontrib>Han, Dong Keun</creatorcontrib><title>Preparation of TGF-β1-conjugated biodegradable pluronic F127 hydrogel and its application with adipose-derived stem cells</title><title>Journal of controlled release</title><addtitle>J Control Release</addtitle><description>In this study, a composite hydrogel using Pluronic F127 derivatives and crosslinked hyaluronic acid (X-HA) was investigated, exploring the benefits in the induction of chondrogenic differentiation of human adipose-derived stem cells (ASCs). F127 was chemically modified through a series of reactions that produced multiple F127 derivatives. A chondrogenic growth factor, transforming growth factor-beta 1 (TGF-β1) was then coupled to the heparin-conjugated F127. X-HA was used as a physical stabilizer of the composite hydrogel (X-HA/F127). The chemical structures of F127 derivatives were analyzed using
1H-NMR and ATR-FTIR. Sol–gel transition of the composite hydrogel was identified at body temperature. The conjugated TGF-β1 was moderately released
in vitro from the composite hydrogel. Cell viability of human ASCs in the hydrogels was about 50% after
in vitro culture for 3
days. As the ASCs/hydrogel were injected into nude mice subcutaneously, DAPI staining of the retrieved constructs showed that ASCs were dispersed through the hydrogel matrix. From the immunofluorescent staining of type II collagen, the TGF-conjugated group exhibited more active green signals than the others. In addition, when those constructs were loaded into the full-thickness defect of rabbit knee articular cartilage, Alcian blue staining identified the formation of cartilaginous matrix from the TGF-conjugated hydrogel. The present work indicated that X-HA/F127 composite hydrogel was thermoreversible and biodegradable, and that the TGF-conjugated hydrogel could be effective in inducing chondrogenesis of human ASCs.
[Display omitted]</description><subject>Absorbable Implants</subject><subject>Adipose Tissue - cytology</subject><subject>Adipose Tissue - drug effects</subject><subject>Animals</subject><subject>Biocompatible Materials - chemistry</subject><subject>Biological and medical sciences</subject><subject>Cartilage, Articular - drug effects</subject><subject>Cell Culture Techniques</subject><subject>Cell Differentiation - drug effects</subject><subject>Chondrogenesis</subject><subject>Conjugation</subject><subject>Disease Models, Animal</subject><subject>Drug Carriers - chemistry</subject><subject>General pharmacology</subject><subject>Human adipose-derived stem cell</subject><subject>Humans</subject><subject>Hydrogels</subject><subject>Medical sciences</subject><subject>Mice</subject><subject>Mice, Nude</subject><subject>Osteochondritis - therapy</subject><subject>Pharmaceutical technology. Pharmaceutical industry</subject><subject>Pharmacology. Drug treatments</subject><subject>Pluronic F127</subject><subject>Poloxamer - chemistry</subject><subject>Rabbits</subject><subject>Stem Cells - cytology</subject><subject>Stem Cells - drug effects</subject><subject>Stem Cells - metabolism</subject><subject>TGF-β1 release</subject><subject>Tissue Engineering</subject><subject>Tissue Scaffolds - chemistry</subject><subject>Transforming Growth Factor beta1 - administration & dosage</subject><subject>Transforming Growth Factor beta1 - pharmacology</subject><subject>Transforming Growth Factor beta1 - therapeutic use</subject><issn>0168-3659</issn><issn>1873-4995</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2010</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFkMFu1DAQhi0EokvhEUC-IE5ZxnYSJyeEKrYgVYJDOVsTe7J1lI2DnRSVx-JBeCa82gWOnEaa-eaf0cfYSwFbAaJ-O2wHG6ZI41ZC7kG9BQmP2EY0WhVl21aP2SZzTaHqqr1gz1IaAKBSpX7KLiRUbVtWYsN-fIk0Y8TFh4mHnt9e74pfP0WRs4d1jws53vngaB_RYTcSn8c1hslbvhNS87sHF8OeRo6T435JHOd59PYU990vdxydn0OiwlH09zktLXTglsYxPWdPehwTvTjXS_Z19-H26mNx8_n609X7m8IqaJeCXK2lVKQr0B0SlkAIrtQAbUV50vQSpXKuBKkqFF0rmroBVLrtaqk1qUv25pQ7x_BtpbSYg0_HD3CisCajqxKgFo3IZHUibQwpRerNHP0B44MRYI7WzWDO1s3RuoHaZOt579X5wtodyP3d-qM5A6_PACaLYx9xsj7945RsGoAmc-9OHGUf956iSdbTZMn5SHYxLvj_vPIb5haj1Q</recordid><startdate>201010</startdate><enddate>201010</enddate><creator>Jung, Hong Hee</creator><creator>Park, Kwideok</creator><creator>Han, Dong Keun</creator><general>Elsevier B.V</general><general>Elsevier</general><scope>IQODW</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope></search><sort><creationdate>201010</creationdate><title>Preparation of TGF-β1-conjugated biodegradable pluronic F127 hydrogel and its application with adipose-derived stem cells</title><author>Jung, Hong Hee ; Park, Kwideok ; Han, Dong Keun</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c309t-ed67223e7507baea40ea0d470095e7228f2a23dd40235a1b918680a379b6277e3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2010</creationdate><topic>Absorbable Implants</topic><topic>Adipose Tissue - cytology</topic><topic>Adipose Tissue - drug effects</topic><topic>Animals</topic><topic>Biocompatible Materials - chemistry</topic><topic>Biological and medical sciences</topic><topic>Cartilage, Articular - drug effects</topic><topic>Cell Culture Techniques</topic><topic>Cell Differentiation - drug effects</topic><topic>Chondrogenesis</topic><topic>Conjugation</topic><topic>Disease Models, Animal</topic><topic>Drug Carriers - chemistry</topic><topic>General pharmacology</topic><topic>Human adipose-derived stem cell</topic><topic>Humans</topic><topic>Hydrogels</topic><topic>Medical sciences</topic><topic>Mice</topic><topic>Mice, Nude</topic><topic>Osteochondritis - therapy</topic><topic>Pharmaceutical technology. Pharmaceutical industry</topic><topic>Pharmacology. Drug treatments</topic><topic>Pluronic F127</topic><topic>Poloxamer - chemistry</topic><topic>Rabbits</topic><topic>Stem Cells - cytology</topic><topic>Stem Cells - drug effects</topic><topic>Stem Cells - metabolism</topic><topic>TGF-β1 release</topic><topic>Tissue Engineering</topic><topic>Tissue Scaffolds - chemistry</topic><topic>Transforming Growth Factor beta1 - administration & dosage</topic><topic>Transforming Growth Factor beta1 - pharmacology</topic><topic>Transforming Growth Factor beta1 - therapeutic use</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Jung, Hong Hee</creatorcontrib><creatorcontrib>Park, Kwideok</creatorcontrib><creatorcontrib>Han, Dong Keun</creatorcontrib><collection>Pascal-Francis</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>Journal of controlled release</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Jung, Hong Hee</au><au>Park, Kwideok</au><au>Han, Dong Keun</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Preparation of TGF-β1-conjugated biodegradable pluronic F127 hydrogel and its application with adipose-derived stem cells</atitle><jtitle>Journal of controlled release</jtitle><addtitle>J Control Release</addtitle><date>2010-10</date><risdate>2010</risdate><volume>147</volume><issue>1</issue><spage>84</spage><epage>91</epage><pages>84-91</pages><issn>0168-3659</issn><eissn>1873-4995</eissn><coden>JCREEC</coden><abstract>In this study, a composite hydrogel using Pluronic F127 derivatives and crosslinked hyaluronic acid (X-HA) was investigated, exploring the benefits in the induction of chondrogenic differentiation of human adipose-derived stem cells (ASCs). F127 was chemically modified through a series of reactions that produced multiple F127 derivatives. A chondrogenic growth factor, transforming growth factor-beta 1 (TGF-β1) was then coupled to the heparin-conjugated F127. X-HA was used as a physical stabilizer of the composite hydrogel (X-HA/F127). The chemical structures of F127 derivatives were analyzed using
1H-NMR and ATR-FTIR. Sol–gel transition of the composite hydrogel was identified at body temperature. The conjugated TGF-β1 was moderately released
in vitro from the composite hydrogel. Cell viability of human ASCs in the hydrogels was about 50% after
in vitro culture for 3
days. As the ASCs/hydrogel were injected into nude mice subcutaneously, DAPI staining of the retrieved constructs showed that ASCs were dispersed through the hydrogel matrix. From the immunofluorescent staining of type II collagen, the TGF-conjugated group exhibited more active green signals than the others. In addition, when those constructs were loaded into the full-thickness defect of rabbit knee articular cartilage, Alcian blue staining identified the formation of cartilaginous matrix from the TGF-conjugated hydrogel. The present work indicated that X-HA/F127 composite hydrogel was thermoreversible and biodegradable, and that the TGF-conjugated hydrogel could be effective in inducing chondrogenesis of human ASCs.
[Display omitted]</abstract><cop>Kidlington</cop><pub>Elsevier B.V</pub><pmid>20599451</pmid><doi>10.1016/j.jconrel.2010.06.020</doi><tpages>8</tpages></addata></record> |
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subjects | Absorbable Implants Adipose Tissue - cytology Adipose Tissue - drug effects Animals Biocompatible Materials - chemistry Biological and medical sciences Cartilage, Articular - drug effects Cell Culture Techniques Cell Differentiation - drug effects Chondrogenesis Conjugation Disease Models, Animal Drug Carriers - chemistry General pharmacology Human adipose-derived stem cell Humans Hydrogels Medical sciences Mice Mice, Nude Osteochondritis - therapy Pharmaceutical technology. Pharmaceutical industry Pharmacology. Drug treatments Pluronic F127 Poloxamer - chemistry Rabbits Stem Cells - cytology Stem Cells - drug effects Stem Cells - metabolism TGF-β1 release Tissue Engineering Tissue Scaffolds - chemistry Transforming Growth Factor beta1 - administration & dosage Transforming Growth Factor beta1 - pharmacology Transforming Growth Factor beta1 - therapeutic use |
title | Preparation of TGF-β1-conjugated biodegradable pluronic F127 hydrogel and its application with adipose-derived stem cells |
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