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Grafting of wool fibers through disulfide bonds: An advanced application of S-protected thiolated starch.
Le, Nguyet-Minh Nguyen; Steinbring, Christian; Matuszczak, Barbara; Baus, Randi Angela; Tribus, Martina; Pham, Tung; Bechtold, Thomas; Bernkop-Schnürch, Andreas.
Affiliation
  • Le NN; Center for Chemistry and Biomedicine, Department of Pharmaceutical Technology, Institute of Pharmacy, University of Innsbruck, Innrain 80/82, 6020 Innsbruck, Austria; Department of Industrial Pharmacy, University of Medicine and Pharmacy, Ho Chi Minh City, Vietnam.
  • Steinbring C; Center for Chemistry and Biomedicine, Department of Pharmaceutical Technology, Institute of Pharmacy, University of Innsbruck, Innrain 80/82, 6020 Innsbruck, Austria.
  • Matuszczak B; Center for Chemistry and Biomedicine, Department of Pharmaceutical Chemistry, Institute of Pharmacy, University of Innsbruck, Innrain 80/82, 6020 Innsbruck, Austria.
  • Baus RA; Center for Chemistry and Biomedicine, Department of Pharmaceutical Technology, Institute of Pharmacy, University of Innsbruck, Innrain 80/82, 6020 Innsbruck, Austria.
  • Tribus M; Center for Chemistry and Biomedicine, Department of Pharmaceutical Chemistry, Institute of Pharmacy, University of Innsbruck, Innrain 80/82, 6020 Innsbruck, Austria.
  • Pham T; Research Institute of Textile Chemistry and Textile Physics, Leopold Franzens-University of Innsbruck, Hoechsterstraße 73, 6850 Dornbirn, Austria.
  • Bechtold T; Research Institute of Textile Chemistry and Textile Physics, Leopold Franzens-University of Innsbruck, Hoechsterstraße 73, 6850 Dornbirn, Austria.
  • Bernkop-Schnürch A; Center for Chemistry and Biomedicine, Department of Pharmaceutical Technology, Institute of Pharmacy, University of Innsbruck, Innrain 80/82, 6020 Innsbruck, Austria. Electronic address: andreas.bernkop@uibk.ac.at.
Int J Biol Macromol ; 147: 473-481, 2020 Mar 15.
Article in En | MEDLINE | ID: mdl-31926921
The purpose of this study is to develop a potential pathway for grafting polymers onto wool fibers based on thiol-disulfide exchange reactions. S-protected thiolated starch (PTS) was synthesized by coupling 3-(2-pyridyldithio) propanoic acid to starch through esterification, resulting in 417.3 ± 15.1 µmol ligand binding to 1 g of starch. PTS was labelled with fluorescein isothiocyanate (FITC) prior to grafting. Wool fibers were preactivated by raising the amount of thiol groups utilizing mild reducing agents. The highest degree of preactivation on the surface of wool fibers was achieved by a 0.2% (w/v) sodium borohydride and 1.5% (w/v) sodium bisulfite mixture pH 5.0 resulting in 182.6 ± 8.7 µmol thiol groups per gram of fibers. Different incubation times and ratios between FITC-labelled PTS and wool fibers were investigated. A graft yield of 58.5% was achieved at a ratio of 1:1.5 (w/w) between wool fibers and FITC-labelled PTS within 18 h of incubation. Successful coating of PTS on wool fibers was confirmed by confocal imaging, scanning electron microscopy and FT-IR. Mechanical properties of grafted wool fibers were tested regarding elongation and tensile strength. These results provide evidence for the potential of S-protected thiolated starch as a superior coating material for wool fibers.
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Starch Language: En Journal: Int J Biol Macromol Year: 2020 Document type: Article Affiliation country: Country of publication:

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Starch Language: En Journal: Int J Biol Macromol Year: 2020 Document type: Article Affiliation country: Country of publication: