Copper mediated and copper free click decoration of polysialic acid for RGD-modification and hydrogel formation

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OriginalspracheEnglisch
Seiten (von - bis)82-91
Seitenumfang10
FachzeitschriftMacromolecular Symposia
Jahrgang334
Ausgabenummer1
PublikationsstatusVeröffentlicht - 18 Dez. 2013

Abstract

Summary This paper describes and compares the copper-catalyzed and copper-free "click" reaction of N-azido, N-alkynoyl and N-oxanorbornadienyl polysialic acid for the formation of hydrogels and cyclic RGD conjugates. To proof the molecular mechanism of the crosslinking reaction, the crosslinking and conjugation reactions were studied in detail on a molecular level by 1H-NMR spectroscopy and mass spectrometry as well as MS/MS experiments identifying the non-hydrolyzable crosslinks.

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Copper mediated and copper free click decoration of polysialic acid for RGD-modification and hydrogel formation. / Su, Yi; Paleček, Jiří; Kirschning, Andreas et al.
in: Macromolecular Symposia, Jahrgang 334, Nr. 1, 18.12.2013, S. 82-91.

Publikation: Beitrag in FachzeitschriftArtikelForschungPeer-Review

Su Y, Paleček J, Kirschning A, Dräger G. Copper mediated and copper free click decoration of polysialic acid for RGD-modification and hydrogel formation. Macromolecular Symposia. 2013 Dez 18;334(1):82-91. doi: 10.1002/masy.201300115
Su, Yi ; Paleček, Jiří ; Kirschning, Andreas et al. / Copper mediated and copper free click decoration of polysialic acid for RGD-modification and hydrogel formation. in: Macromolecular Symposia. 2013 ; Jahrgang 334, Nr. 1. S. 82-91.
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AU - Kirschning, Andreas

AU - Dräger, Gerald

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AB - Summary This paper describes and compares the copper-catalyzed and copper-free "click" reaction of N-azido, N-alkynoyl and N-oxanorbornadienyl polysialic acid for the formation of hydrogels and cyclic RGD conjugates. To proof the molecular mechanism of the crosslinking reaction, the crosslinking and conjugation reactions were studied in detail on a molecular level by 1H-NMR spectroscopy and mass spectrometry as well as MS/MS experiments identifying the non-hydrolyzable crosslinks.

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