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Dive into the research topics where Kurt Ingar Draget is active.

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Featured researches published by Kurt Ingar Draget.


Carbohydrate Polymers | 1994

Alginic acid gels: the effect of alginate chemical composition and molecular weight

Kurt Ingar Draget; G. Skjåk Bræk; Olav Smidsrød

Abstract The effect of chemical composition and sequence and molecular weight of different alginate samples on the final properties of alginic acid gels have been studied. It is shown that alginates with a high content of guluronic acid blocks give gels of a considerably higher strength compared to alginates rich in mannuronate. A high fraction of homopolymeric blocks seems to favour the formation of junction zones. Compared to Ca-alginate gels, a more extended molecular weight dependent regime is observed. Kinetic measurements show an initially rapid (∼30 min) sol-gel transition with an apparent equilibrium in the dynamic storage moduli gradually obtained within 24–48 h, depending on the chemical composition of the alginate sample used. Mechanical spectroscopy reveals gels with a high degree of solid-like nature, with an increasing frequency dependence with decreasing molecular weight.


Biomaterials | 1992

Chitosan cross-linked with Mo(VI) polyoxyanions : a new gelling system

Kurt Ingar Draget; Kjell M. Vårum; Einar Moen; Hege Gynnild; Olav Smidsrød

A procedure for preparing homogeneous chitosan gels by in situ molybdate cross-linking is described. The gels are obtained by dispersing solid MoO3 in a buffered chitosan solution and the polymer is cross-linked by formation of heavily negatively charged molybdate polyoxyanions. The resulting ionic gels are very transparent, thermoirreversible and can be made at low polymer concentrations. Depending on the ionic strength, these gels are able to swell several times their original size in aqueous solutions. Estimates of the degree of cross-linking reveal a very open pore structure which is confirmed by electron micrographs of the gel.


Carbohydrate Polymers | 1992

Temperature dependence of the elastic modulus of alginate gels

Størker T. Moe; Kurt Ingar Draget; Gudmund Skjåk-Bræk; Olav Simdsrød

Abstract The temperature dependence of the elastic modulus for alginate gels was studied using two different gel systems: covalently crosslinked Na-alginate gels and in-situ prepared Ca-alginate gels. The modulus of physically crosslinked gels showed a complex behaviour. The temperature coefficient of the modulus of covalently crosslink gels changed from positive for the lowest crosslinked gels to negative for the highest crosslinked gels. This suggests a change from rubberlike to enthalpy-driven elasticity with an increasing degree of crosslinking for these gel networks.


Archive | 2014

Investigation of Physico-Chemical Properties of Gelatin Matrices in Correlation with Dissolution Studies

Magnus N. Hattrem; Silje Molnes; Kurt Ingar Draget

Gelatin is a versatile biopolymer obtained from a partial hydrolysis of collagen. Gelatin is commonly used in formulation of pharmaceuticals and nutraceuticals, encapsulating the active ingredient. For these applications the dissolution profile of the matrix in the gastrointestinal tract (GIT) is of crucial importance. The dissolution of a gelatin matrix in the GIT may be seen as a two-step procedure: gel-sol transition of the gelatin network, followed by diffusion of the peptide strands from the concentrated matrix to the bulk liquid. Thus, it is clear that the melting temperature is important in gelatin gel dissolution investigations. Depending on the raw material (bovine or porcine sources) and extraction conditions, gelatins with wide variations in molecular size distribution – and therefore varying rheological properties/melting temperatures – may be obtained. Dissolution studies are generally time consuming and therefore it would be advantageous to predict the dissolution profile without performing in vitro measurements. The scope of this work was to evaluate if any of the physico-chemical properties of the gelatin matrices can be used to predict the dissolution profiles of the gelatin gels.


Archive | 2011

Chapter 7:Alginates: Existing and Potential Biotechnological and Medical Applications

Kurt Ingar Draget; Gudmund Skjåk-Bræk

The present chapter on alginates in biotechnology and medicine comprises a description of traditional uses where alginates have been used as devices in e.g. wound dressings, as well as an in-depth introduction to possible future applications. The latter area is based on new scientific information on the immunostimulating properties of certain alginate sequences, as well as on the popularity gained by the alginate as immobilization matrix for cells. The latter opens up the use of alginate encapsulated cells for specific cell transplantation provided that the properties of the capsules are properly understood and controlled.


Archive | 2014

Gelatins – Physicochemical Properties, Source Dependence and Applications

Magnus N. Hattrem; Kurt Ingar Draget

With an estimated annual world-wide production of more than 300xa0000 metric tonnes, gelatin is one of the most abundant commercial biopolymers, and also one of the most versatile with several hundred different applications, from technical to pharmaceutical. Production of gelatin is based on a partial hydrolysis of the mother structural molecule collagen. Mammalian (homoeothermic) sources of gelatin have basically identical amino acid composition and physical properties, although gelatins (and collagens) from poikilothermic animals may vary considerably.


Archive | 1998

Procedure for producing uronic acid blocks from alginate

Merethe Kamfjord Simensen; Olav Smidsr.o slashed.d; Kurt Ingar Draget; Finn Hjelland


Archive | 1997

Use of g-block polysaccharides

Merethe Kamfjord Simensen; Edvar Onsoyen; Kurt Ingar Draget; Olav Smidsrod; Therese Fjaereide


Archive | 2009

CHEWABLE GELLED EMULSIONS

Tore Seternes; Kurt Ingar Draget; Ingvild Johanne Haug


Archive | 2009

Soft gel capsules

Ingvild Johanne Haug; Kurt Ingar Draget

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Ingvild Johanne Haug

Norwegian University of Science and Technology

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Tore Seternes

Norwegian College of Fishery Science

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Magnus N. Hattrem

Norwegian University of Science and Technology

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Catherine Taylor

Norwegian University of Science and Technology

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Gudmund Skjåk-Bræk

Norwegian University of Science and Technology

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Kjell M. Vårum

Norwegian Institute of Technology

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Olav Smidsrød

Norwegian University of Science and Technology

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Einar Moen

Norwegian Institute of Technology

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G. Skjåk Bræk

Norwegian Institute of Technology

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