Functionalised type-I collagen as a hydrogel building block for bio-orthogonal tissue engineering applicationsElectronic supplementary information (ESI) available: Details of methacrylated collagen synthesis and characterization after modification, including the fabrication of thiol-Michael hydrogels by varying the concentration of crosslinkers; details about structural elucidation, gelation time and mechanical properties measurement of hydrogels, and details about enzymatic degradation, in vitr
In this study, we derivatized type I collagen without altering its triple helical conformation to allow for facile hydrogel formation via the Michael addition of thiols to methacrylates without the addition of other crosslinking agents. This method provides the flexibility needed for the fabrication...
Gespeichert in:
Hauptverfasser: | , , , , , , , , |
---|---|
Format: | Artikel |
Sprache: | |
Online-Zugang: | Volltext |
Tags: |
Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
|
container_end_page | 326 |
---|---|
container_issue | 2 |
container_start_page | 318 |
container_title | |
container_volume | 4 |
creator | Ravichandran, R Islam, M. M Alarcon, E. I Samanta, A Wang, S Lundström, P Hilborn, J Griffith, M Phopase, J |
description | In this study, we derivatized type I collagen without altering its triple helical conformation to allow for facile hydrogel formation
via
the Michael addition of thiols to methacrylates without the addition of other crosslinking agents. This method provides the flexibility needed for the fabrication of injectable hydrogels or pre-fabricated implantable scaffolds, using the same components by tuning the modulus from Pa to kPa. Enzymatic degradability of the hydrogels can also be easily fine-tuned by variation of the ratio and the type of the cross-linking component. The structural morphology reveals a lamellar structure mimicking native collagen fibrils. The versatility of this material is demonstrated by its use as a pre-fabricated substrate for culturing human corneal epithelial cells and as an injectable hydrogel for 3-D encapsulation of cardiac progenitor cells.
Modulating the hydrogel properties from injectable to implantable scaffolds using the bio-orthogonal thiol-Michael addition click reaction. |
doi_str_mv | 10.1039/c5tb02035b |
format | Article |
fullrecord | <record><control><sourceid>rsc</sourceid><recordid>TN_cdi_rsc_primary_c5tb02035b</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>c5tb02035b</sourcerecordid><originalsourceid>FETCH-rsc_primary_c5tb02035b3</originalsourceid><addsrcrecordid>eNqFUs1u1DAQDggkKuiFO9IcQWpKtsvCAkfYih56ggO3auJMkqGOHc04K6XPzQMwSdMgTvhiezzf38hZ9nJTnG-K7ce3bpfK4qLY7srH2clFsSvyD7vN_sl6Ln4-y05VfxW29pv3--27k0e_L4fgEseAnpUqSGNP-RW46D02FAAVENqxktiQh3JgX3FooPTR3UIdBUqOeZTUxmbigMSqAwGFhgORTL3Y954dTiJ68OSSxMAOdLA6dRQSyggcjKybm-D14fvVG8AjssfS0yf4SsnOCrGGjlKLTkaPydyuNnUMqSVlcxus3KKgSyZ_d8-ItV2gixXXi5MzU3R-mMMYEmosZXmaZFLL0efXbEwW-yG_QjnC0ew-oFwMzgLIinMSVT2HWxL9DNXiG8s4JNAkg0uD2JTID46rxYgR3-MTdzT778h0bUbW2UvsSRKTWhV1kHlik9Rq6mzG_KtF4W6cpums3ghWa2Y4cpIX2dMavdLpsj_PXl0efnz5lou6m164s4g3f3_T9n_vfwDEMOF8</addsrcrecordid><sourcetype>Publisher</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype></control><display><type>article</type><title>Functionalised type-I collagen as a hydrogel building block for bio-orthogonal tissue engineering applicationsElectronic supplementary information (ESI) available: Details of methacrylated collagen synthesis and characterization after modification, including the fabrication of thiol-Michael hydrogels by varying the concentration of crosslinkers; details about structural elucidation, gelation time and mechanical properties measurement of hydrogels, and details about enzymatic degradation, in vitr</title><source>Royal Society Of Chemistry Journals</source><source>Alma/SFX Local Collection</source><creator>Ravichandran, R ; Islam, M. M ; Alarcon, E. I ; Samanta, A ; Wang, S ; Lundström, P ; Hilborn, J ; Griffith, M ; Phopase, J</creator><creatorcontrib>Ravichandran, R ; Islam, M. M ; Alarcon, E. I ; Samanta, A ; Wang, S ; Lundström, P ; Hilborn, J ; Griffith, M ; Phopase, J</creatorcontrib><description>In this study, we derivatized type I collagen without altering its triple helical conformation to allow for facile hydrogel formation
via
the Michael addition of thiols to methacrylates without the addition of other crosslinking agents. This method provides the flexibility needed for the fabrication of injectable hydrogels or pre-fabricated implantable scaffolds, using the same components by tuning the modulus from Pa to kPa. Enzymatic degradability of the hydrogels can also be easily fine-tuned by variation of the ratio and the type of the cross-linking component. The structural morphology reveals a lamellar structure mimicking native collagen fibrils. The versatility of this material is demonstrated by its use as a pre-fabricated substrate for culturing human corneal epithelial cells and as an injectable hydrogel for 3-D encapsulation of cardiac progenitor cells.
Modulating the hydrogel properties from injectable to implantable scaffolds using the bio-orthogonal thiol-Michael addition click reaction.</description><identifier>ISSN: 2050-750X</identifier><identifier>EISSN: 2050-7518</identifier><identifier>DOI: 10.1039/c5tb02035b</identifier><creationdate>2015-12</creationdate><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>315,782,786,27933,27934</link.rule.ids></links><search><creatorcontrib>Ravichandran, R</creatorcontrib><creatorcontrib>Islam, M. M</creatorcontrib><creatorcontrib>Alarcon, E. I</creatorcontrib><creatorcontrib>Samanta, A</creatorcontrib><creatorcontrib>Wang, S</creatorcontrib><creatorcontrib>Lundström, P</creatorcontrib><creatorcontrib>Hilborn, J</creatorcontrib><creatorcontrib>Griffith, M</creatorcontrib><creatorcontrib>Phopase, J</creatorcontrib><title>Functionalised type-I collagen as a hydrogel building block for bio-orthogonal tissue engineering applicationsElectronic supplementary information (ESI) available: Details of methacrylated collagen synthesis and characterization after modification, including the fabrication of thiol-Michael hydrogels by varying the concentration of crosslinkers; details about structural elucidation, gelation time and mechanical properties measurement of hydrogels, and details about enzymatic degradation, in vitr</title><description>In this study, we derivatized type I collagen without altering its triple helical conformation to allow for facile hydrogel formation
via
the Michael addition of thiols to methacrylates without the addition of other crosslinking agents. This method provides the flexibility needed for the fabrication of injectable hydrogels or pre-fabricated implantable scaffolds, using the same components by tuning the modulus from Pa to kPa. Enzymatic degradability of the hydrogels can also be easily fine-tuned by variation of the ratio and the type of the cross-linking component. The structural morphology reveals a lamellar structure mimicking native collagen fibrils. The versatility of this material is demonstrated by its use as a pre-fabricated substrate for culturing human corneal epithelial cells and as an injectable hydrogel for 3-D encapsulation of cardiac progenitor cells.
Modulating the hydrogel properties from injectable to implantable scaffolds using the bio-orthogonal thiol-Michael addition click reaction.</description><issn>2050-750X</issn><issn>2050-7518</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2015</creationdate><recordtype>article</recordtype><sourceid/><recordid>eNqFUs1u1DAQDggkKuiFO9IcQWpKtsvCAkfYih56ggO3auJMkqGOHc04K6XPzQMwSdMgTvhiezzf38hZ9nJTnG-K7ce3bpfK4qLY7srH2clFsSvyD7vN_sl6Ln4-y05VfxW29pv3--27k0e_L4fgEseAnpUqSGNP-RW46D02FAAVENqxktiQh3JgX3FooPTR3UIdBUqOeZTUxmbigMSqAwGFhgORTL3Y954dTiJ68OSSxMAOdLA6dRQSyggcjKybm-D14fvVG8AjssfS0yf4SsnOCrGGjlKLTkaPydyuNnUMqSVlcxus3KKgSyZ_d8-ItV2gixXXi5MzU3R-mMMYEmosZXmaZFLL0efXbEwW-yG_QjnC0ew-oFwMzgLIinMSVT2HWxL9DNXiG8s4JNAkg0uD2JTID46rxYgR3-MTdzT778h0bUbW2UvsSRKTWhV1kHlik9Rq6mzG_KtF4W6cpums3ghWa2Y4cpIX2dMavdLpsj_PXl0efnz5lou6m164s4g3f3_T9n_vfwDEMOF8</recordid><startdate>20151223</startdate><enddate>20151223</enddate><creator>Ravichandran, R</creator><creator>Islam, M. M</creator><creator>Alarcon, E. I</creator><creator>Samanta, A</creator><creator>Wang, S</creator><creator>Lundström, P</creator><creator>Hilborn, J</creator><creator>Griffith, M</creator><creator>Phopase, J</creator><scope/></search><sort><creationdate>20151223</creationdate><title>Functionalised type-I collagen as a hydrogel building block for bio-orthogonal tissue engineering applicationsElectronic supplementary information (ESI) available: Details of methacrylated collagen synthesis and characterization after modification, including the fabrication of thiol-Michael hydrogels by varying the concentration of crosslinkers; details about structural elucidation, gelation time and mechanical properties measurement of hydrogels, and details about enzymatic degradation, in vitr</title><author>Ravichandran, R ; Islam, M. M ; Alarcon, E. I ; Samanta, A ; Wang, S ; Lundström, P ; Hilborn, J ; Griffith, M ; Phopase, J</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-rsc_primary_c5tb02035b3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><creationdate>2015</creationdate><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Ravichandran, R</creatorcontrib><creatorcontrib>Islam, M. M</creatorcontrib><creatorcontrib>Alarcon, E. I</creatorcontrib><creatorcontrib>Samanta, A</creatorcontrib><creatorcontrib>Wang, S</creatorcontrib><creatorcontrib>Lundström, P</creatorcontrib><creatorcontrib>Hilborn, J</creatorcontrib><creatorcontrib>Griffith, M</creatorcontrib><creatorcontrib>Phopase, J</creatorcontrib></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Ravichandran, R</au><au>Islam, M. M</au><au>Alarcon, E. I</au><au>Samanta, A</au><au>Wang, S</au><au>Lundström, P</au><au>Hilborn, J</au><au>Griffith, M</au><au>Phopase, J</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Functionalised type-I collagen as a hydrogel building block for bio-orthogonal tissue engineering applicationsElectronic supplementary information (ESI) available: Details of methacrylated collagen synthesis and characterization after modification, including the fabrication of thiol-Michael hydrogels by varying the concentration of crosslinkers; details about structural elucidation, gelation time and mechanical properties measurement of hydrogels, and details about enzymatic degradation, in vitr</atitle><date>2015-12-23</date><risdate>2015</risdate><volume>4</volume><issue>2</issue><spage>318</spage><epage>326</epage><pages>318-326</pages><issn>2050-750X</issn><eissn>2050-7518</eissn><abstract>In this study, we derivatized type I collagen without altering its triple helical conformation to allow for facile hydrogel formation
via
the Michael addition of thiols to methacrylates without the addition of other crosslinking agents. This method provides the flexibility needed for the fabrication of injectable hydrogels or pre-fabricated implantable scaffolds, using the same components by tuning the modulus from Pa to kPa. Enzymatic degradability of the hydrogels can also be easily fine-tuned by variation of the ratio and the type of the cross-linking component. The structural morphology reveals a lamellar structure mimicking native collagen fibrils. The versatility of this material is demonstrated by its use as a pre-fabricated substrate for culturing human corneal epithelial cells and as an injectable hydrogel for 3-D encapsulation of cardiac progenitor cells.
Modulating the hydrogel properties from injectable to implantable scaffolds using the bio-orthogonal thiol-Michael addition click reaction.</abstract><doi>10.1039/c5tb02035b</doi><tpages>9</tpages></addata></record> |
fulltext | fulltext |
identifier | ISSN: 2050-750X |
ispartof | |
issn | 2050-750X 2050-7518 |
language | |
recordid | cdi_rsc_primary_c5tb02035b |
source | Royal Society Of Chemistry Journals; Alma/SFX Local Collection |
title | Functionalised type-I collagen as a hydrogel building block for bio-orthogonal tissue engineering applicationsElectronic supplementary information (ESI) available: Details of methacrylated collagen synthesis and characterization after modification, including the fabrication of thiol-Michael hydrogels by varying the concentration of crosslinkers; details about structural elucidation, gelation time and mechanical properties measurement of hydrogels, and details about enzymatic degradation, in vitr |
url | https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2024-12-01T23%3A51%3A14IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-rsc&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Functionalised%20type-I%20collagen%20as%20a%20hydrogel%20building%20block%20for%20bio-orthogonal%20tissue%20engineering%20applicationsElectronic%20supplementary%20information%20(ESI)%20available:%20Details%20of%20methacrylated%20collagen%20synthesis%20and%20characterization%20after%20modification,%20including%20the%20fabrication%20of%20thiol-Michael%20hydrogels%20by%20varying%20the%20concentration%20of%20crosslinkers;%20details%20about%20structural%20elucidation,%20gelation%20time%20and%20mechanical%20properties%20measurement%20of%20hydrogels,%20and%20details%20about%20enzymatic%20degradation,%20in%20vitr&rft.au=Ravichandran,%20R&rft.date=2015-12-23&rft.volume=4&rft.issue=2&rft.spage=318&rft.epage=326&rft.pages=318-326&rft.issn=2050-750X&rft.eissn=2050-7518&rft_id=info:doi/10.1039/c5tb02035b&rft_dat=%3Crsc%3Ec5tb02035b%3C/rsc%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_id=info:pmid/&rfr_iscdi=true |