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• W2023966428 endingPage "1250" @default.
• W2023966428 startingPage "1239" @default.
• W2023966428 abstract "In this study we chemospecifically functionalized alginate with thiol-ended peptides for tissue engineering (TE); a carbodiimide linker and the disulfide exchange scheme were used. First carboxyls of alginate were activated by introducing N-hydroxysuccinimide (NHS) ester groups; these react with primary amines of the heterobifunctional reagent 2-(2-pyridyldithio)ethyleneamine (PDEA). Thiol-reactive alginate (alginate-S-S-py) forms as cross-linking intermediate. The degree of pyridyldithio-functionalization is modified through variable PDEA concentration and it was determined using UV–VIS spectroscopy and proton nuclear magnetic resonance. The applicability of the alginate-S-S-py as platform for the chemoselective coupling of thiol-ended peptides was tested with glutathione as model peptide. Other SH-terminal peptides were successfully cross-linked. Moreover, the peptide–alginate keeps its gel-forming ability when treated with Ca2+ cations, leading to functionalized hydrogels that can be further used to obtain different multicomponent systems. The developed chemoselective strategy of functionalizing alginate with thiol-ended peptides could enhance the potential of this polymer for TE." @default.
• W2023966428 created "2016-06-24" @default.
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• W2023966428 date "2012-05-01" @default.
• W2023966428 modified "2023-10-16" @default.
• W2023966428 title "Chemoselective cross-linking of alginate with thiol-terminated peptides for tissue engineering applications" @default.
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• W2023966428 doi "https://doi.org/10.1016/j.carbpol.2012.01.089" @default.
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