Exchange resins cellulosic

Food dyes are extracted from foods by using adsorbents such as wool fibers, powdered polyamide, cellulose exchange resins, or RP cartridges (Sep-pak Cis), which is the method of choice for a fast and easy cleanup. After desorption of the colorants and filtration, the solution is analyzed by either ion-pair or reversed-phase LC. Ion-pair LC uses water acetone mixtures (80 20) with tetrabutylammonium chloride added as ion-pair agent and Cig or Cg columns. As for RPLC, a combination of phosphate buffer methanol, water acetonitrile, and methanokacetone are commonly used. Gradients are used to allow the separation of the different classes of... 

Although the interest in, and application of layer chromatography has historically resulted from the development of PC, it was soon replaced by thin-layer chromatography (TLC). In PC, only one stationary phase matrix is available (cellulose), at variance to TLC (silica, polyamide, ion-exchange resins, cellulose). Using a silica-gel plate, separation of a sample can be accomplished in approximately 1 h as compared with many hours on paper. The plate size is much smaller than the necessary paper size. Also, more samples can be spotted... 

Epoxy resin (Tufnol, Bakelite, Epophen) Styrene divinylbenzene ion exchange resins Reillex HPQ anion exchange resin Phenol/formaldehyde cation exchange resin Polyurethane Cellulose (as tissues)... 

Sensors based on the above reaction scheme have been developed for Al3+, Zn2+, Cu2+, Ca2+, Pb2+, Hg2"1", K+, Li+, etc. A polycation, protamine sensor has also been developed using 2/7/-dichlorofluorescein octadecyl ester (DCFOE) doped in polymer membranes. However, most of these sensors are pH dependent due to the pH dependence of the cation complexation reactions. The cation ion indicators can be immobilized on any solid support, such as silica, cellulose, ion-exchange resin, porous glass, sol-gel, or entrapped in polymer membranes. 

Ion-exchange resins are cross-linked polymers which are typically polystyrene, cellulose or agarose based. Polystyrene is hydrophobic in nature and useful for inorganic ions and small molecules while cellulose and agarose are hydrophilic and more useful for the larger, biologically important molecules, e.g. proteins and nucleic acids, which either would be adversely affected by a hydrophobic environment or could not gain access to the small pore structure. 

Since the reaction has been reviewed recently (12) only a few additional facts will be mentioned. Many optically active cyanohydrins can be prepared (33) with e.e. s of 84 to 100% by the use of the flavopnotein D-oxynitrilase adsorbed on special (34) cellulose ion-exchange resins. Although the enzyme is stable, permitting the use of a continuously operating column, naturally only one enantiomer, usually the R isomer, is produced in excess. This (reversible) enzyme-catalyzed reaction is very rapid (34). Nonenzymic catalysts, such as the cinchona alkaloids, permit either enantiomer to be prepared in excess. 

Filtrasorb 300 Filtrasorb 300 Activated charcoal Anion-exchange resin Cation-exchange resin Cellulose powder Cellulose triacetate Kaolinite... 

Some of the exchanged resins were coated with cellulose acetate butyrate or cellulose acetate phthalate. The results showed relaxation rate enhancement in 25% water suspensions containing 2% carboxymethylcellulose (CMC) as a surfactant. The relaxivities, however, were rather low. It should be noted, however, that the measurements were made at high field, 300 MHz, where the relaxivity enhancements are always smaller. 

Since protein adsorption to an anion exchange resin is reversible and does not constitute a classical immobilization, the ability of the resins to retain activity under various conditions must be determined. Macrosorb KAX DEAE bound -D-glucosidase was tested with solutions of primary interest for their final application. Several batch washes of a 1% w/v slurry were required to ensure complete equilibrium elution for a given concentration, as determined from the absence of pNPG units in subsequent washes. Several salt solutions of typical fermentation media components were tested. These included 3 mM to 50 mM solutions of MgSO, KHgPO, NaQ, and sodium acetate. Also, incubations with cellulase solutions were tested to determine if the proteins present in a cellulose hydrolysis would displace the -D-glucosidase. Both of these displacement studies were carried out at 22°C and 40 C. 

---