Spatially resolved coding of λ-orthogonal hydrogels by laser lithography

Batchelor, RR; Blasco, E; Wuest, KNR; Lu, H; Wegener, M; Barner-Kowollik, C; Stenzel, MH

Spatially resolved coding of λ-orthogonal hydrogels by laser lithography

Batchelor, RR Blasco, E Wuest, KNR Lu, H

Wegener, M Barner-Kowollik, C Stenzel, MH

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Publication Type:: Journal Article
Citation:: Chemical Communications, 2018, 54 (19), pp. 2436 - 2439
Issue Date:: 2018-01-01

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Field	Value	Language
dc.contributor.author	Batchelor, RR	en_US
dc.contributor.author	Blasco, E	en_US
dc.contributor.author	Wuest, KNR	en_US
dc.contributor.author	Lu, H https://orcid.org/0000-0001-6932-1900	en_US
dc.contributor.author	Wegener, M	en_US
dc.contributor.author	Barner-Kowollik, C	en_US
dc.contributor.author	Stenzel, MH	en_US
dc.date.issued	2018-01-01	en_US
dc.identifier.citation	Chemical Communications, 2018, 54 (19), pp. 2436 - 2439	en_US
dc.identifier.issn	1359-7345	en_US
dc.identifier.uri	http://hdl.handle.net/10453/134094
dc.description.abstract	© 2018 The Royal Society of Chemistry. A λ-orthogonal reaction system is introduced, where visible light induced radical thiol-ene and UV light induced NITEC (Nitrile-Imine mediated Tetrazole-Ene Conjugation) ligations are consecutively employed to fabricate and functionalize PEG-based hydrogels. The fluorescent pyrazoline cycloadducts from the NITEC reaction are exploited to visualize the written structures within the hydrogels as well as to attach RGD containing functional groups to promote spatially resolved cell attachment on the hydrogel surface.	en_US
dc.relation.ispartof	Chemical Communications	en_US
dc.relation.isbasedon	10.1039/c7cc09619d	en_US
dc.subject.classification	Organic Chemistry	en_US
dc.title	Spatially resolved coding of λ-orthogonal hydrogels by laser lithography	en_US
dc.type	Journal Article
utslib.citation.volume	19	en_US
utslib.citation.volume	54	en_US
utslib.for	0305 Organic Chemistry	en_US
utslib.for	03 Chemical Sciences	en_US
pubs.embargo.period	Not known	en_US
pubs.organisational-group	/University of Technology Sydney
pubs.organisational-group	/University of Technology Sydney/Faculty of Science
pubs.organisational-group	/University of Technology Sydney/Faculty of Science/School of Mathematical and Physical Sciences
pubs.organisational-group	/University of Technology Sydney/Strength - IBMD - Initiative for Biomedical Devices
utslib.copyright.status	closed_access
pubs.issue	19	en_US
pubs.publication-status	Published	en_US
pubs.volume	54	en_US

Abstract:

© 2018 The Royal Society of Chemistry. A λ-orthogonal reaction system is introduced, where visible light induced radical thiol-ene and UV light induced NITEC (Nitrile-Imine mediated Tetrazole-Ene Conjugation) ligations are consecutively employed to fabricate and functionalize PEG-based hydrogels. The fluorescent pyrazoline cycloadducts from the NITEC reaction are exploited to visualize the written structures within the hydrogels as well as to attach RGD containing functional groups to promote spatially resolved cell attachment on the hydrogel surface.

Please use this identifier to cite or link to this item:

http://hdl.handle.net/10453/134094