1986
DOI: 10.1002/apmc.1986.051440116
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Immobilization of trypsin on poly(alginic acid‐g‐glycidyl methacrylate‐co‐hydroxy ethyl methacrylate)

Abstract: To synthesize a matrix for the immobilization of enzymes, alginic acid, a naturally occurring polysaccharide has been chosen as the backbone, and glycidyl methacrylate (GMA) and 2‐hydroxy ethyl methacrylate (HEMA) as monomers for graft copolymerization. HEMA was used to introduce hydrophilic character which would have been lost during the introduction of the hydrophobic monomer glycidyl methacrylate into alginic acid. Immobilization of trypsin onto this matrix takes place by covalent bonding. The temperature o… Show more

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Cited by 7 publications
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“…A singlet at 8.63 ppm was observed due to azomethine proton [8,9]. Multiple signals in the region of 6.50-8.40 ppm are assigned to aromatic protons [10][11].…”
Section: H Nmr Spectramentioning
confidence: 99%
“…A singlet at 8.63 ppm was observed due to azomethine proton [8,9]. Multiple signals in the region of 6.50-8.40 ppm are assigned to aromatic protons [10][11].…”
Section: H Nmr Spectramentioning
confidence: 99%