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...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Hauptverfasser: Ravichandran, R, Islam, M. M, Alarcon, E. I, Samanta, A, Wang, S, Lundström, P, Hilborn, J, Griffith, M, Phopase, J
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