Injectable Glycosaminoglycan-Based Cryogels from Well-Defined Microscale Templates for Local Growth Factor Delivery

dc.bibliographicCitation.firstPage1178eng
dc.bibliographicCitation.issue7eng
dc.bibliographicCitation.journalTitleACS Chemical Neuroscienceeng
dc.bibliographicCitation.lastPage1188eng
dc.bibliographicCitation.volume12eng
dc.contributor.authorNewland, Ben
dc.contributor.authorNewland, Heike
dc.contributor.authorLorenzi, Francesca
dc.contributor.authorEigel, Dimitri
dc.contributor.authorDieter FischerWelzel, Petra B.
dc.contributor.authorFischer, Dieter
dc.contributor.authorWang, Wenxin
dc.contributor.authorFreudenberg, Uwe
dc.contributor.authorRosser, Anne
dc.contributor.authorWerner, Carsten
dc.date.accessioned2021-11-23T07:51:57Z
dc.date.available2021-11-23T07:51:57Z
dc.date.issued2021
dc.description.abstractGlycosaminoglycan-based hydrogels hold great potential for applications in tissue engineering and regenerative medicine. By mimicking the natural extracellular matrix processes of growth factor binding and release, such hydrogels can be used as a sustained delivery device for growth factors. Since neural networks commonly follow well-defined, high-aspect-ratio paths through the central and peripheral nervous system, we sought to create a fiber-like, elongated growth factor delivery system. Cryogels, with networks formed at subzero temperatures, are well-suited for the creation of high-aspect-ratio biomaterials, because they have a macroporous structure making them mechanically robust (for ease of handling) yet soft and highly compressible (for interfacing with brain tissue). Unlike hydrogels, cryogels can be synthesized in advance of their use, stored with ease, and rehydrated quickly to their original shape. Herein, we use solvent-assisted microcontact molding to form sacrificial templates, in which we produced highly porous cryogel microscale scaffolds with a well-defined elongated shape via the photopolymerization of poly(ethylene glycol) diacrylate and maleimide-functionalized heparin. Dissolution of the template yielded cryogels that could load nerve growth factor (NGF) and release it over a period of 2 weeks, causing neurite outgrowth in PC12 cell cultures. This microscale template-assisted synthesis technique allows tight control over the cryogel scaffold dimensions for high reproducibility and ease of injection through fine gauge needles. ©eng
dc.description.versionpublishedVersioneng
dc.identifier.urihttps://oa.tib.eu/renate/handle/123456789/7394
dc.identifier.urihttps://doi.org/10.34657/6441
dc.language.isoengeng
dc.publisherWashington, DC : ACS Publicationseng
dc.relation.doihttps://doi.org/10.1021/acschemneuro.1c00005
dc.relation.essn1948-7193
dc.rights.licenseCC BY 4.0 Unportedeng
dc.rights.urihttps://creativecommons.org/licenses/by/4.0/eng
dc.subject.ddc540eng
dc.subject.othercryogel scaffoldeng
dc.subject.otherHeparineng
dc.subject.othernerve growth factoreng
dc.subject.otherPC12 cellseng
dc.subject.otherphotopolymerizationeng
dc.subject.othersustained deliveryeng
dc.titleInjectable Glycosaminoglycan-Based Cryogels from Well-Defined Microscale Templates for Local Growth Factor Deliveryeng
dc.typeArticleeng
dc.typeTexteng
tib.accessRightsopenAccesseng
wgl.contributorIPFeng
wgl.subjectChemieeng
wgl.typeZeitschriftenartikeleng
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