Jamie Mistry
University of Birmingham
Medical Textiles and Biomaterials for Healthcare | 2006
Mohsen Miraftab; G. Smart; John F. Kennedy; Charles J. Knill; Jamie Mistry; M.R. Groocock
ABSTRACT A range of commercial chitosans were sourced and their molecular size profiles and degrees of acetylation (DA) were determined by HPSEC and 1 H-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.
Medical Textiles and Biomaterials for Healthcare | 2006
John F. Kennedy; Charles J. Knill; Jamie Mistry; Mohsen Miraftab; G. Smart; M.R. Groocock
ABSTRACT A range of commercial chitosans were subjected to controlled acid hydrolysis and their molecular size profiles and degrees of acetylation (DA) were determined (post-hydrolysis) by HPSEC and 1 H-NMR spectroscopy, respectively. Hydrolysed chitosans were subsequently utilised for modification of alginic acid/sodium alginate fibres, and levels of hydrolysed chitosan incorporated into base fibres were estimated by elemental analysis. Tensile properties (elongation % and tenacity) of resultant chitosan/alginate fibres were also determined. A broad range of hydrolysed chitosan contents (˜ 7-25 % w/w) were obtained (significantly higher than using unhydrolysed chitosans). Fibres produced from either alginate A1 (6%), using HCl (0.2M), a draw ratio of 1.18, treated with hydrolysed chitosan C3 (3.9%), or from alginate A3 (4%), using HCl (0.5M), a draw ratio of 1.18, treated with hydrolysed chitosan C3 (3%), had the best properties.
Carbohydrate Polymers | 2004
Charles J. Knill; John F. Kennedy; Jamie Mistry; Mohsen Miraftab; G. Smart; Melanie Rachel Groocock; H. J. Williams
Carbohydrate Polymers | 1990
Jamie Mistry; John F. Kennedy
Journal of Chemical Technology & Biotechnology | 2005
Charles J. Knill; John F. Kennedy; Jamie Mistry; M Miraftab; G Smart; Groocock; Hj Williams
Carbohydrate Polymers | 2003
Jamie Mistry; John F. Kennedy
Carbohydrate Polymers | 2003
John F. Kennedy; Jamie Mistry
Carbohydrate Polymers | 2003
John F. Kennedy; Jamie Mistry
Carbohydrate Polymers | 2004
John F. Kennedy; Jamie Mistry
Carbohydrate Polymers | 2004
Jamie Mistry; John F. Kennedy