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E High-Performance Liquid Chromatography

Albert K, Bayer E. High-performance liquid chromatography proton nuclear magnetic resonance on-line coupling. In Patonay G, ed. HPLC Detection, Newer Methods. New York VCH, 1992 197-227. [Pg.342]

Davies, M. Smith, K.D. Harbin, A.M. Hounsell, E.E. High-performance liquid chromatography of oligosaccharide alditols and glycopeptides on a graphitized 53. carbon column. J. Chromatogr., A 1992, 609 (1,2), 125-... [Pg.1253]

Lin, J.-T. Heftmann, E. High-performance liquid chromatography of naturally occurring estrogens. J.Chromatogr, 1981, 212, 239-244... [Pg.578]

Jeannot, R. and Sauvard, E., High performance liquid chromatography coupled with mass spectrometry applied to analyses of pesticides in water, Analusis, 27, 271-280, 1999. [Pg.1025]

E.D. Katz (Ed.), High Performance Liquid Chromatography Principles and Methods in Biotechnology, J. Wiley Sons, Chichester, 1996. ISBN 0471934445. [Pg.48]

In 1972, Kirkland at E. I. du Pont de Nemours patented porous silica microspheres (PSM) specifically for high-performance liquid chromatography (HPLC) applications (3). Prior to this development, silica particles used for chromatographic applications were simply adapted from some other use. In the 1970s, Kirkland showed that porous silica particles could be used for size-... [Pg.75]

New types of ion exchange resins have also been developed to meet the specific needs of high-performance liquid chromatography (HPLC) (Chapter 8). These include pellicular resins and microparticle packings (e.g. the Aminex-type resins produced by Bio-Rad). A review of the care, use and application of the various ion exchange packings available for HPLC is given in Ref. 19. [Pg.188]

Figure 3 depicts profiles of Total PAH fluxes vs. time (36). The following polycyclic hydrocarbons have been determined by high performance liquid chromatography, variable wavelength absorption detection Naphthalene, acenaphthylene, 7,12-dimethylbenzanthracene, 2-methylnaphtalene, fluorene, acenaphtene, phenanthrene, 2,3-dimethylnaphtalene, anthracene, fluoranthene, 1-methylphenanthrene, pyrene, 2,3-benzofluorene, triphenylene, benz(a)anthracene, chrysene, benzo(b)fluoranthene, benzo(k)fluoranthene, perylene, benzo(e)pyrene, 1,2,3,4-dibenzanthracene, benzo(a)pyrene, and 1,2,5,6-dibenzanthracene. [Pg.295]

De Schryver E, De Reu L, Willems JL. 1985. Determination of methyl paraoxon in dog plasma by reversed-phased high performance liquid chromatography. J Chromatogr 338 389-395. [Pg.201]

BAILEY R G, NURSTEN H E and MCDOWELL I (1991) Comparative study of the reversed-phase high-performance liquid chromatography of black tea liquids with special reference to the thearubigins , J Chromatogr A, 542, 115-28. [Pg.150]

BRONNER w E and BEECHER G R (1998) Method for determining the content of catechins in tea infusions by high-performance liquid chromatography , J Chromatogr A, 805, 137-42. [Pg.150]

GUO c, CAO G, SOFIC E and PRIOR R L (1997) High-performance liquid Chromatography coupled with coulometric array detection of electroactive components in fruits and vegetables Relationship to oxygen radical absorbance capacity, J Agric Food Chem, 45, 1787-96. [Pg.342]

LAZARUS s E, ADAMSON G E, HAMMERSTONE J F and SCHMITZ H H (1999) High-performance liquid chromatography/Mass spectrometry analysis of proanthocyanidins in foods and beverages, JAgric Food Chem, 47, 3693-701. [Pg.343]

Herbach, K.M., Stintzing, E.C., and Carle, R., Thermal degradation of betacyanins in juices from purple pitaya (Hylocereus polyrhizus [Weber] Britton Rose) monitored by high-performance liquid-chromatography-tandem mass spectrometric analyses, Fur. Food Res. TechnoL, 219, 377, 2004. [Pg.95]

Mitcham, E.J., Gross, K.C., and Wasserman, B.P. (1991) Synthesis of uridinediphospho-[U- C]-D-galacturonic acid by enzyme particulate fractions and purification via high performance liquid chromatography. Phytochem.Anal. 2 112-115. [Pg.124]

Lipophilicity represents the affinity of a molecule or a moiety for a lipophilic environment. It is commonly measured by its distribution behavior in a biphasic system, either liquid-liquid (e.g. partition coefficient in 1-octanol-water) or solid-liquid (retention on reversed-phase high-performance liquid chromatography or thin-layer chromatography system). [Pg.35]

In modern times, most analyses are performed on an analytical instrument for, e.g., gas chromatography (GC), high-performance liquid chromatography (HPLC), ultra-violet/visible (UV) or infrared (IR) spectrophotometry, atomic absorption spectrometry, inductively coupled plasma mass spectrometry (ICP-MS), mass spectrometry. Each of these instruments has a limitation on the amount of an analyte that they can detect. This limitation can be expressed as the IDL, which may be defined as the smallest amount of an analyte that can be reliably detected or differentiated from the background on an instrument. [Pg.63]

M.E. Lacey, Z. J. Tan, A. G. Webb, J. V. Sweedler 2001, (Union of capillary high-performance liquid chromatography and microcoil nuclear magnetic resonance spectroscopy applied to the separation and identification of terpenoids), J. Chromatogr. A 922(1-2), 139. [Pg.139]

Renn, C. N. and Synovec, R. E., Packed microcapillary columns in high performance liquid chromatography, Anal. Chem., 63, 568, 1991. [Pg.50]

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