M. MiraftabG. SmartJ. F. KennedyC. J. KnillJ. MistryM. R. Groocock
A range of commercial chitosans were sourced and their molecular size profiles and degrees of acetylation (DA) were determined by HPSEC and 1H-NMR spectroscopy, respectively. Chitosans were subsequently utilised for modification of alginate fibres, and levels of chitosan incorporated into base fibres were estimated by elemental analysis. Elongation (%) and tenacity of resultant chitosan/alginate fibres were determined in order to assess their potential application in wound dressings. A range of chitosan contents (˜ 0-6 % w/w) resulted from a variety of alginate and chitosan starting materials. Fibres produced from sodium alginate (A1, 6%) using hydrochloric acid (0.2M) at a draw ratio of 1.18, and treated with chitosan (C1, 3.2%) were deemed to have the best properties. In general, use of a water washing stage resulted in the production of better chitosan/alginate fibres. Treatment with chitosans generally resulted in a reduction in tenacity (and a reduction in % elongation if a water washing stage was not used), i.e. no increase in fibre strength was observed, implying that the chitosan is more like a coating rather than penetrating/reinforcing the alginate fibre.
Mohsen MiraftabG. SmartJohn F. KennedyCharles J. KnillJ MistryM.R. Groocock
Miguel P. BatistaV.S.S. GonçalvesFrédéric Bustos GasparIsabel NogueiraAna A. MatiasPavel Gurikov
Yuliana Dwi RachmawatiFiska Yohana Purwaningtyas
Charles J. KnillJ. F. KennedyJ MistryMohsen MiraftabG. SmartM.R. GroocockH.J Williams