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Classical gels

Classical gels had a low degree of cross-linkage and were of a large particle size. This resulted in that modest flow rates could only be applied and the separation time was typically 10 hr, which at that time was perfectly acceptable, keeping in mind that preparation of the column could take up to 2 days or more. After the introduction of Sephadex, new materials have been introduced continuously on the market, and still, 30 years after the introduction of the first commercial material, new media are still introduced, also from the originators of Sephadex. What are the driving forces behind this development and what are the features of these new media ... [Pg.27]

Recently, the separation of some milligram quantities of terbutaline by classical gel electrophoresis has been reported [194]. A sulfated cyclodextrin impregnated on the agarose gel was used as a chiral selector and the complete resolution was achieved in 5 h. Analogously, small amounts of enantiomers can be isolated using thin-layer... [Pg.16]

Classical gel electrophoresis has been used extensively for protein and nucleic acid purification and characterization [9, 10], but has not been used routinely for small molecule separations, other than for polypeptides. A comparison between TLC and electrophoresis reveals that while detection is usually accomplished off-line in both electrophoretic and TLC methods, the analyte remains localized in the TLC bed and the mobile phase is immediately removed subsequent to chromatographic development. In contrast, in gel electrophoresis, the gel matrix serves primarily as an anti-... [Pg.289]

Ultimately, however, it should be noted that these examples of classical gel electrophoretic separations are batch processes and therefore limited in sample throughput. To achieve true preparative-scale separations by electrophoresis, it becomes necessary to convert to continuous processes. [Pg.292]

Preparative continuous free flow electrophoresis was first reported in 1958 [15]. As in the case of classical gel electrophoresis, most of the work done in this area has been primarily in the purification of biopolymers. Continuous free flow electrophoresis for the separation of small molecules has remained relatively unexplored [16], although this is beginning to change. [Pg.292]

In a different approach, Stalcup and co-workers [25] used sulfated (3-cyclodextrin for the enantioseparation of piperoxan in work directly derived from earlier CE and classical gel results. Their results were obtained using a continuous free flow apparatus developed by R S Technologies, Inc. Processing rates on the order of 4.5 mg h were reported. [Pg.294]

An alternative approach to transdermal drug application that differs from patches and classic gels led to the foundation of Acrux, an Australian drug delivery company. The key finding was that certain widely used sunscreens, including Cs- to Cis-alkyl substituted-cinnamate,... [Pg.255]

This work describes a new type of monolithic support offering a highly interconnected permanent porosity possessing pendant double bond. This support may provide a better accessibility to active sites and allows the use of a wider range of solvents than classical gel type beads prepared by suspension polymerisation. The free radical addition of functional thiols led to the production of functional supports (acid, ester, alcohol, amine, thiol...). [Pg.131]

These are the familiar classical gel points and have already been derived by Spouge [48] in a different context. The result of Eq. (48) is a quite natural consequence, since we are dealing with the hypothetical situation of an infinitely concentrated solution where the ring fraction is infinitely scarce so that the ideal tree model practically applies. [Pg.162]

When generalizing this reasoning to include ring formation, we may expect that the ideal tree model with no excluded volume and no ring formation will be realized in the limit C. The classical gel theory corresponds to this limiting case (C—). That is thus comparable to the classic status of the ideal gas law (C—>0) to the real gas. [Pg.195]

Solid lines (—) Eq. (102). (O) classical gel points (0) critical dilution. Experimental... [Pg.200]

Fig. 23. Comparison of theory and experiment Dc vs. y [z / mol] curve The figure shown in the right side box is a magnification of the same plot. Solid lines (—) Eq. (102). (O) classical gel points ((x)) critical dilution. Experimental points by Muller and coworkers [67] (O k = 1)... Fig. 23. Comparison of theory and experiment Dc vs. y [z / mol] curve The figure shown in the right side box is a magnification of the same plot. Solid lines (—) Eq. (102). (O) classical gel points ((x)) critical dilution. Experimental points by Muller and coworkers [67] (O k = 1)...
Electrophoretic methods are widely used alternatives for the analytical determination of the enantiomeric purity of chiral compounds [194]. Due to the high elTi-ciency of capillary electrophoresis, separations can be achieved even when very low selectivities are observed. At a preparative scale, these methods are well established for the purification of proteins and cells [195] but there is very little published on enantioselective separations. Only recently, some interest in chiral preparative applications has been manifested. Separation of the enantiomers ofterbu-taline [196] and piperoxan [197] have been reported by classical gel electrophoresis using sulfated cyclodextrin as a chiral additive, while the separation of the enantiomers of methadone could be successfully achieved by using free-fluid isotachophoresis [198] and by applying a process called interval-flow electrophoresis [199]. [Pg.181]

Fig. 4.6.7. (Left) Simple glass column for classical gel chromatography. 1, eluent inlet 2, connecting adaptor 3, mobile phase 4, filter paper 5, gel bed 6, glass spheres 100-200 iim 7, sintered glass plate 8, glass spheres 0.2-2 mm 9. stopcock. Fig. 4.6.7. (Left) Simple glass column for classical gel chromatography. 1, eluent inlet 2, connecting adaptor 3, mobile phase 4, filter paper 5, gel bed 6, glass spheres 100-200 iim 7, sintered glass plate 8, glass spheres 0.2-2 mm 9. stopcock.
This group includes several related techniques such as classical gel electrophoresis, field-flow fractionation (FFF) and the capillary techniques capillary zone electrophoresis (CZE), capillary electrokinetic chromatography (CEKC) capillary isotachophoresis (CUP), capillary isoelectric focusing (CIEF) and capillary electrochromatography (CEC). [Pg.164]

Classical gel electrophoresis is well-established for the purification and preparation of charged compounds of biological importance such as peptides, nucleic acids, etc. However, it... [Pg.164]

In gels, cross-links withstand concentration fluctuations and classic gels are characterized by high transparency. [Pg.249]

Figure 20.11. PRDF Ti for silica aerogels doped with titania at 5 mol% sonogel (continuous thin line), classic gel (dashed line) and anatase (continuous bold line). Adapted with permission from [32]. Figure 20.11. PRDF Ti for silica aerogels doped with titania at 5 mol% sonogel (continuous thin line), classic gel (dashed line) and anatase (continuous bold line). Adapted with permission from [32].

See other pages where Classical gels is mentioned: [Pg.290]    [Pg.290]    [Pg.529]    [Pg.300]    [Pg.300]    [Pg.46]    [Pg.87]    [Pg.189]    [Pg.111]    [Pg.153]    [Pg.305]    [Pg.146]    [Pg.139]    [Pg.145]    [Pg.184]    [Pg.265]    [Pg.227]    [Pg.166]    [Pg.230]    [Pg.135]    [Pg.330]    [Pg.886]    [Pg.265]    [Pg.359]    [Pg.90]    [Pg.1503]    [Pg.147]   
See also in sourсe #XX -- [ Pg.148 ]




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Classic Theory for Gels

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