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Liquid chromatography range

Figure 7.5 The Enhanced Fluidity Liquid Chromatography range. This occupies the volume in the phase diagram below the locus of critical temperatures, above and below the locus of critical pressures, and is composed mostly of the less volatile mobile-phase component. Reproduced by permission of the American Chemical Society. Figure 7.5 The Enhanced Fluidity Liquid Chromatography range. This occupies the volume in the phase diagram below the locus of critical temperatures, above and below the locus of critical pressures, and is composed mostly of the less volatile mobile-phase component. Reproduced by permission of the American Chemical Society.
Liquid chromatography was performed on symmetry 5 p.m (100 X 4.6 mm i.d) column at 40°C. The mobile phase consisted of acetronitrile 0.043 M H PO (36 63, v/v) adjusted to pH 6.7 with 5 M NaOH and pumped at a flow rate of 1.2 ml/min. Detection of clarithromycin and azithromycin as an internal standard (I.S) was monitored on an electrochemical detector operated at a potential of 0.85 Volt. Each analysis required no longer than 14 min. Quantitation over the range of 0.05 - 5.0 p.g/ml was made by correlating peak area ratio of the dmg to that of the I.S versus concentration. A linear relationship was verified as indicated by a correlation coefficient, r, better than 0.999. [Pg.395]

SynChropak GPC supports were introduced in 1978 as the first commercial columns for high-performance liquid chromatography of proteins. SynChropak GPC columns were based on research developed by Fred Regnier and coworkers in 1976 (1,2). The first columns were only available in 10-yu,m particles with a 100-A pore diameter, but as silica technology advanced, the range of available pore diameters increased and 5-yu,m particle diameters became available. SynChropak GPC and CATSEC occasionally were prepared on larger particles on a custom basis, but generally these products have been intended for analytical applications. [Pg.305]

Bonded-phase chromatography (BPC). To overcome some of the problems associated with conventional LLC, such as loss of stationary phase from the support material, the stationary phase may be chemically bonded to the support material. This form of liquid chromatography, in which both monomeric and polymeric phases have been bonded to a wide range of support materials, is termed bonded-phase chromatography . [Pg.219]

General Description. Liquid chromatography encompasses any chromatographic method in which the mobile phase is a liquid (c.f. gas chromatography). A variety of stationary phases and retention mechanisms are available such that a broad range of modes of separation are possible. It is worthwhile to briefly describe the important modes that find use in clinical chemistry. [Pg.227]

A UV spectrum with a pronounced absorption above 210 nm allows UV detection after liquid chromatography (LC), but an absorption maximum in the range of visible light may also decompose during cleanup procedures and require the elimination of light when handling extracts. [Pg.53]


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Liquid ranges

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