Uptake of tridodecylmethylammonium chloride by PVC

The uptake of tridodecylmethylammonium chloride (TDMAC) by poly(vinyl chloride) has been investigated to provide a more quantitative basis for the preparation of blood-compatible surfaces based on TDMAC-heparin coatings. Sorption isotherms of TDMAC from toluene-cyclohexane and toluene-methanol mixtures have been measured. In toluene-cyclohexane mixtures, the TDMAC uptake is proportional to the degree of swelling of the polymer. From ion-exchange experiments with 36Cl-, it appears that only a small fraction of the TDMAC remains near the PVC surface to provide the heparin binding capacity. Methanol forms a strong H-bonded complex with TDMAC in toluence and prevents its sorption by PVC

Synthetic polymers with anticoagulant activity

Polymers with C=C bonds have been modified by reaction with chlorosulfonyl isocyanate (CSI). Addition products were obtained in yields varying from 60% to 75%. Reaction of these products with NaOH yielded polyelectrolytes with sulfamate and carboxylate groups, whereas from the reaction with NH4OH polyelectrolytes with sulfamate and carbonamide groups, were obtained. The polyelectrolytes showed anticoagulant activity depending on the structure and on the presence of both sulfamate and carboxylate groups. These groups are essential for the anticoagulant activity, because N-S bond cleavage in the sulfamate groups as well as substitution of carboxylate by carbonamide groups resulted in loss of activity. From the recalcification times of bovine plasma, it could be concluded that the most active polyelectrolyte had an activity of 6-7% compared with heparin. However, determination of the activated clotting time of blood from rabbits showed that this compound had an in vivo activity of 50% in comparison with heparin

Blends of Amphiphilic, Hyperbranched Polyesters and Different Polyolefins

A hyperbranched polyester based on 3,5-dihydroxybenzoic acid was completely modified with dodecanoyl chloride to result in an amphiphilic, globular polymer, which has a polar core and a nonpolar outer sphere with the ability both to incorporate an organic dye and to interact with a nonpolar matrix. A series of blends were prepared using either polypropylene or polyethylene (HDPE) as the matrix. The content of the polyester as disperse phase was varied between 0.05 and 20 wt %. The blends with polyester contents up to 5% were prepared for colorization of polyolefins using the polyester as a dye carrier. The blends with higher polyester contents were prepared in order to investigate the influence of the hyperbranched material on the material properties. The blends exhibited a heterogeneous morphology with very small particle sizes even at high polyester concentrations. The melt rheology measurements resulted in a reduced complex viscosity for both polyolefins when the hyperbranched polyester was added. The observed melt viscosity of the i-PP blends deviated from the linear mixing rule, whereas the HDPE blends followed it. The use of amphiphilic hyperbranched polyesters as dye carriers allowed a homogeneous distribution of an organic dye in a polyolefin matrix with similar dynamic-mechanical behavior of the blends compared to the case of pure polyolefins. The dyed samples exhibited good stability in extraction experiments.