Column chromatography interactions

The separation of xanthates by ion-interaction reversed-phase column chromatography is described for the determination of eight different xanthates in reagents commonly used in flotation plants. The separated species were detected spectroscopically at a wavelength of 305 nm (96). 

A reliable chromatographic method has been developed for the quantitative aneilysis of hydrophobic impurities in water-soluble polymeric dyes. The method utilizes both the molecular sieve effect of normal gel permeation chromatography and solute-column packing interaction, modified by solvent composition. This method eliminates the need to extract the impurities from the polymeric dye with 100 extraction efficiency, as would be required for an ordinary liquid chromatographic analysis. 

Hydrophobic interaction chromatography (HIC) is a column chromatography technique which can determine particle hydrophobicity by interaction with a hydrophobic gel matrix [142,149,150]. Hydrophilic particles pass through the column without interaction, whereas particles with increased hydrophobicity show a retarded elution and are retained by the column. Hydrophobicity measurements are used to determine the hydrophobicity of nanoparticulate carriers and correlate this to their in vivo biodistribution [10, 149]. 

Interest in the nature of interactions between shortchain organic surfactants and large molecular weight macromolecules and ions with hydroxyapatite extends to several fields. In the area of carles prevention and control, surfactant adsorption plays an important role in the Initial states of plaque formation (1-5) and in the adhesion of tooth restorative materials ( ). Interaction of hydroxyapatite with polypeptides in human urine is important in human biology as hydroxyapatite has been found as a major or minor component in a majority of kidney stones ( 7). Hydroxyapatite is used in column chromatography as a material for separating proteins (8-9). The flotation separation of apatite from... 

The relevance of LSC data to reverse osmosis stems from the physicochemical basis (adsorption equilibrium considerations) of liquid-solid chromatography (52), and the principle that the solute-solvent-membrane material (column material) Interactions governing the relative retention times of solutes in LSC are analogous to the interactions prevailing at the membrane-solution Interface under reverse osmosis conditions. The work already reported in several papers on the subject (53-58) indicate that the foregoing principle is valid, and hence LSC data offer an appropriate means of characterizing interfacial properties of membrane materials, and understanding solute separations in reverse osmosis. 

While polydisperse model systems can nicely be resolved, the reconstruction of a broad and skewed molar mass distribution is only possible within certain limits. At this point, experimental techniques in which only a nonexponential time signal or some other integral quantity is measured and the underlying distribution is obtained from e.g. an inverse Laplace transform are inferior to fractionating techniques, like size exclusion chromatography or the field-flow fractionation techniques. The latter suffer, however, from other problems, like calibration or column-solute interaction. 

Quinones-Torrelo et al. (1999 2001) have demonstrated a correlation of pharmacokinetic properties with results from micellar liquid chromatography. In this method micellar solutions of nonionic surfactants are used as the mobile phase in reverse-phase liquid chromatography. Interactions between the mobile and stationary phases are purported to correspond to the membrane/water interface of biological barriers as hydrophobic, steric, and electronic interactions are important for both. For a series of 18 antihistamines Quinones-Torrelo et al. (2001) showed that both volume of distribution and half-life values were better correlated with retention on these columns than with the classical log K, w descriptor. 

In the previous chapters we have examined the two factors that must be considered to understand how separations occur. One is the kinetic factor that describes how analyte molecules spread into an increasingly wide zone during their transport through the chromatographic bed. The other is the thermodynamic factor that explains the interactions between analyte and the chromatographic phases resulting in differential sorption or retention in the bed. In this chapter we will combine these two factors and see how a separation is effected. For simplicity, the discussion will be limited to column chromatography. 

Column chromatography uses an open vertical glass column, with a solid support (e.g., silica gel or alumina) which can interact weakly with a mixture of analytes dissolved in a liquid eluant, which is fed through the column by gravity. It is used as an inexpensive separation technique, even on a preparative scale. 

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