concanavalin-a has been researched along with methacrylamide* in 3 studies
3 other study(ies) available for concanavalin-a and methacrylamide
Article | Year |
---|---|
Effect of varying molecular weight of dextran on acrylic-derivatized dextran and concanavalin A glucose-responsive materials for closed-loop insulin delivery.
Dextran methacrylate (dex-MA) and concanavalin A (con A)-methacrylamide were photopolymerized to produce covalently cross-linked glucose-sensitive gels for the basis of an implantable closed-loop insulin delivery device.. The viscoelastic properties of these polymerized gels were tested rheologically in the non-destructive oscillatory mode within the linear viscoelastic range at glucose concentrations between 0 and 5% (w/w).. For each cross-linked gel, as the glucose concentration was raised, a decrease in storage modulus, loss modulus and complex viscosity (compared at 1 Hz) was observed, indicating that these materials were glucose responsive. The higher molecular weight acrylic-derivatized dextrans [degree of substitution (DS) 3 and 8%] produced higher complex viscosities across the glucose concentration range.. These studies coupled with in vitro diffusion experiments show that dex-MA of 70 kDa and DS (3%) was the optimum mass average molar mass to produce gels that show reduced component leach, glucose responsiveness, and insulin transport useful as part of a self-regulating insulin delivery device. Topics: Acrylamides; Concanavalin A; Dextrans; Diffusion; Drug Delivery Systems; Feedback, Physiological; Gels; Glucose; Hypoglycemic Agents; Infusion Pumps, Implantable; Insulin; Methacrylates; Molecular Weight; Temperature; Viscosity | 2011 |
UV cross-linked dextran methacrylate--concanavalin A methacrylamide gel materials for self-regulated insulin delivery.
In this study, the successful acrylic derivatization of dextran and concanavalin A (con A) to form dextran methacrylate and con A methacrylamide is shown. These derivatized acrylic monomers are then photopolymerized in the presence of a water soluble photoinitiator Irgacure under various conditions to form covalently bonded glucose-responsive gel materials, which undergo a transformation to sol in the presence of free glucose. Rheological data have revealed that as the degree of substitution for dextran methacrylate is increased, a more elastic material is produced due to the increased covalent linkages. Some of these gel systems show negligible component loss in in vitro diffusion experiments used to simulate the behavior of the cross-linked gel, as would be used in a self-regulated insulin delivery device. Topics: Acrylamides; Concanavalin A; Dextrans; Elasticity; Gels; Hypoglycemic Agents; Insulin; Methacrylates; Molecular Weight; Polymers; Propane; Rheology; Solubility; Spectroscopy, Fourier Transform Infrared; Technology, Pharmaceutical; Temperature; Ultraviolet Rays | 2008 |
Development of a reversed-phase high-performance liquid chromatography method for the analysis of components from a closed-loop insulin delivery system.
A reversed-phase HPLC method has been developed which enables separation of the three components of a closed-loop insulin delivery system, namely concanavalin A methacrylamide (Con A-MA), dextran methacrylate (Dex-MA) and bovine insulin. The analysis of Con A-MA represents a significant challenge due to the formation of multiple conformations on contact with the chromatographic surface and the mobile phase. The extent of conformational change is shown to be dependent on a number of parameters: column temperature, mobile phase pH, contact time with the chromatographic surface, salt type and concentration and the organic modifier. By manipulation of these variables, protein denaturation can be minimised and recovery improved. Topics: Acrylamides; Animals; Chromatography, High Pressure Liquid; Concanavalin A; Dextrans; Humans; Hydrogen-Ion Concentration; Insulin; Insulin Infusion Systems; Protein Conformation; Reproducibility of Results; Temperature | 2006 |