Catalase Immobilized on Poly(Acrylic Acid-co-Vinyl Alcohol)

The paper studies the reaction of catalase’s immobilization on a synthetic polymer (copolymer of the acrylic acid with vinyl alcohol), through amidation of enzyme’s terminal amine groups with the lateral carboxylic group of the macromolecular support, as activated by dicycloxexyl carbodiimide. The support, possessing the properties of a hydrogel, has been synthesized through copolymerization of the acrylic acid with vinyl acetate, followed by hydrolysis of the acetate groups to the hydroxylic groups. The influence of some reaction parameters (such as the activator/support and enzyme/support ratios, duration) on the efficiency of the enzyme’s coupling was studied. The coupling reactions were realized conformely to a centered, rotator, composed, second order experimental program, which permitted the establishment of the conditions necessary for obtaining a coupling product containing the highest amount of immobilized enzyme. Kinetic study of the reaction catalyzed by the coupling products has indirectly evidenced enzyme’s immobilization to the macromolecular support, and also, a sufficiently high catalytic activity of the enzymatic preparation obtained

Furazolidone Immobilized in a Hydrogel Based on Crosslinked Carboxymethyl Cellulose

The paper deals with the obtainment of a polymer-drug system with controlled release of the biological active principle, based on furazolidone included in a hydrogel obtained by crosslinking of carboxymethylcellulose with epichlorohydrine. The influence of temperature and duration of crosslinking reaction on the crosslinking degree of carboxymethylcellulose (indirectly appreciated by its swelling capacity in polar liquids as water and dimethylformamide/water mixtures) is studied. Kinetic data concerning the inclusion of furazolidone from solution, in the hydrogel of crosslinked carboxymethylcellulose, as well as the release of the drug from the obtained polymer-drug system, are performed. The obtained results evidence that the inclusion rate as well as the amount of furazolidone diffused into the support depend on the dymethylformamide/ water ratio utilized as solvent, and on the drug concentration in solution. The product obtained through the insertion of furazolidone from a DMF/water mixture = 5/1 (with a content of 8.9 mg drug/hydrogel) was studied as to the kinetics of the active principle’s release, in vitro, by using as an eluent a buffer solution, which simulates the gastric fluid (pH = 2.4). The experimental results prove the obtention of a polymerdrug system with controlled release of the biologically active principle, conform to a zero order kinetic, in the time interval ranging between 3 – 12 hours