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A Generic Strategy for Co‐Presentation of Heparin‐Binding Growth Factors Based on CVD Polymerization

dc.contributor.authorDeng, Xiaopeien_US
dc.contributor.authorLahann, Joergen_US
dc.date.accessioned2012-10-02T17:20:28Z
dc.date.available2013-10-18T17:47:29Zen_US
dc.date.issued2012-09-14en_US
dc.identifier.citationDeng, Xiaopei; Lahann, Joerg (2012). "A Generic Strategy for Co‐Presentation of Heparin‐Binding Growth Factors Based on CVD Polymerization." Macromolecular Rapid Communications 33(17): 1459-1465. <http://hdl.handle.net/2027.42/93760>en_US
dc.identifier.issn1022-1336en_US
dc.identifier.issn1521-3927en_US
dc.identifier.urihttps://hdl.handle.net/2027.42/93760
dc.description.abstractA multifunctional copolymer with both aldehyde and alkyne groups is synthesized by chemical vapor deposition (CVD) for orthogonal co‐immobilization of biomolecules. Surface analytical methods including FTIR and XPS are used to confirm the surface modification. Heparin‐binding growth factors [basic fibroblast growth factor (bFGF) in this study] can be immobilized through interaction with heparin, which was covalently attached to the CVD surface through an aldehyde‐hydrazide reaction. In parallel, an alkyne–azide reaction is used to orthogonally co‐immobilize an adhesion peptide as the second biomolecule. A generic strategy for immobilizing heparin‐binding growth factors on multifunctional chemical vapor deposition copolymer has been developed. Heparin is covalently attached to the aldehyde‐functionalized surface through a carbohydrazide linker. The growth factor then binds directly to the heparin. The alkyne group can then be used to orthogonally immobilize other biomolecule, such as azido‐functionalized adhesion peptides.en_US
dc.publisherWILEY‐VCH Verlagen_US
dc.subject.otherBiomaterialsen_US
dc.subject.otherCoatingsen_US
dc.subject.otherImmobilizationen_US
dc.subject.otherBiomoleculesen_US
dc.subject.otherSurface Engineeringen_US
dc.titleA Generic Strategy for Co‐Presentation of Heparin‐Binding Growth Factors Based on CVD Polymerizationen_US
dc.typeArticleen_US
dc.rights.robotsIndexNoFollowen_US
dc.subject.hlbsecondlevelChemical Engineeringen_US
dc.subject.hlbsecondlevelChemistryen_US
dc.subject.hlbsecondlevelMaterials Science and Engineeringen_US
dc.subject.hlbsecondlevelBiological Chemistryen_US
dc.subject.hlbtoplevelEngineeringen_US
dc.subject.hlbtoplevelHealth Sciencesen_US
dc.subject.hlbtoplevelScienceen_US
dc.description.peerreviewedPeer Revieweden_US
dc.contributor.affiliationumDepartments of Chemical Engineering, Materials Science and Engineering, Macromolecular Science and Engineering and Biomedical Engineering, University of Michigan, Ann Arbor, MI 48109, USA; Institute of Functional Interfaces, Karlsruhe Institute of Technology, Hermann‐von‐Helmholtz‐Platz 1, 76344 Eggenstein‐Leopoldshafen, Germany.en_US
dc.contributor.affiliationumMacromolecular Science and Engineering, University of Michigan, Ann Arbor, MI 48109, USAen_US
dc.contributor.affiliationumDepartments of Chemical Engineering, Materials Science and Engineering, Macromolecular Science and Engineering and Biomedical Engineering, University of Michigan, Ann Arbor, MI 48109, USA; Institute of Functional Interfaces, Karlsruhe Institute of Technology, Hermann‐von‐Helmholtz‐Platz 1, 76344 Eggenstein‐Leopoldshafen, Germanyen_US
dc.identifier.pmid22887691en_US
dc.description.bitstreamurlhttp://deepblue.lib.umich.edu/bitstream/2027.42/93760/1/1459_ftp.pdf
dc.identifier.doi10.1002/marc.201200343en_US
dc.identifier.sourceMacromolecular Rapid Communicationsen_US
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dc.owningcollnameInterdisciplinary and Peer-Reviewed


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