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High-performance liquid instrumentation

Instrumentation High-performance liquid chromatographic determination... [Pg.532]

VAM Instrumentation Working Group, Guidance on the Equipment Qualification of Analytical Instruments High Performance Liquid Chromatography (HPLC), 1998. [Pg.80]

Kondo, F. Identification and analysis of remnant antibiotics by analytical instruments. High performance liquid chromatography, gas chromatography, and enzyme immunoassay. Chikusan no Kenkyu, 42(5), 579-84 42(6) 705-9. 1988. Japanese. [Pg.346]

Figure 9.6 Surfer-generated chromatoeletropherogram of fluorescamine-labeled tryptic digest of ovalbumin. Reprinted from Analytical Chemistry, 62, M. M. Bushey and J. W. Jorgenson, Automated instrumentation for comprehensive two-dimensional high-performance liquid chromatography/capillary zone electrophoresis, pp 978-984, copyright 1990, with permission from the American Chemical Society. Figure 9.6 Surfer-generated chromatoeletropherogram of fluorescamine-labeled tryptic digest of ovalbumin. Reprinted from Analytical Chemistry, 62, M. M. Bushey and J. W. Jorgenson, Automated instrumentation for comprehensive two-dimensional high-performance liquid chromatography/capillary zone electrophoresis, pp 978-984, copyright 1990, with permission from the American Chemical Society.
J F K Huber (Ed), Instrumentation for High Performance Liquid Chromatography, Elsevier, Amsterdam, 1978... [Pg.252]

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]

The spectrum of new analytical techniques includes superior separation techniques and sophisticated detection methods. Most of the novel instruments are hyphenated, where the separation and detection elements are combined, allowing efficient use of materials sometimes available only in minute quantities. The hyphenated techniques also significantly increase the information content of the analysis. Recent developments in separation sciences are directed towards micro-analytical techniques, including capillary gas chromatography, microbore high performance liquid chromatography, and capillary electrophoresis. [Pg.386]

Capillary electrophoresis employing chiral selectors has been shown to be a useful analytical method to separate enantiomers. Conventionally, instrumental chiral separations have been achieved by gas chromatography and by high performance liquid chromatography.127 In recent years, there has been considerable activity in the separation and characterization of racemic pharmaceuticals by high performance capillary electrophoresis, with particular interest paid to using this technique in modem pharmaceutical analytical laboratories.128 130 The most frequently used chiral selectors in CE are cyclodextrins, crown ethers, chiral surfactants, bile acids, and protein-filled... [Pg.405]

N. A. Parris, Instrumental Liquid Chromatography, a Practical Manual on High-Performance Liquid Chromatographic Methods (Journal of Chromatography Library, Vol. 27), Elsevier, Amsterdam, 2nd revised ed., 1984 J. Drozd, Chemical Derivatization in Gas Chromatography (Journal of Chromatography Library, Vol. 19), Elsevier, Amsterdam, 1981 J. F. Lawrence and... [Pg.375]

Chemical Testing. Adequate instrumentation for a variety of different test methods should be available. Most stability-indicating chemical assays are performed by high-performance liquid chromatography. Occasionally, gas chromatography, infrared spectrophotometry, or spectrofluorimetry are used. Test... [Pg.168]

High performance liquid chromatography is a technique that has arisen from the application to liquid chromatography (lc) of theories and instrumentation that were originally developed for gas chromatography (gc). [Pg.16]

It was known from gas chromatographic theory that efficiency could be improved if the particle size of the stationary phase materials used in lc could be reduced. High performance liquid chromatography developed steadily during the late 1960s as these high efficiency materials were produced, and as improvements in instrumentation allowed the full potential of these materials to be realised. As hplc has developed, the particle size of the stationary phase used has... [Pg.17]

The arrangement of the basic components in a high performance liquid chromatograph is described and the sources of dead volume in the instrument are indicated. Typical working pressures and flow rates are given. [Pg.256]

Bushey, M.M., Jorgenson, J.W. (1990). Automated instrumentation for comprehensive two-dimensional high-performance liquid chromatography of proteins. Anal. Chem. 62,161-167. Cabrera, K. (2004). Applications of silica-based monolithic HPLC columns. J. Sep. Sci. 27, 843-852. [Pg.171]

High performance liquid chromatography (HPLC) and capillary electrophoresis (CE) are two instrumental separation techniques that are applicable to the separation of proteins and peptides. The advantage of HPLC and CE techniques is that they afford the analyst the freedom to resolve a complex mixture by different routes employing different... [Pg.365]

Parallel to the development of mass spectrometric instrumentation and methodologies, the improvements of separation techniques, such as gas chromatography (GC), high performance liquid chromatography (HPLC) and capillary electrophoresis (CE), and of their coupling with MS allowed the study of complex mixtures, that are generally encountered in most studies. [Pg.38]

High performance liquid chromatography is used to determine the purity of calcitriol, and to separate it from related compounds. Using a 10 micron silica column of 25 cm length, and a mobile phase of spectroquality heptane ethyl acetate. methanol (50 50 1) at a flow rate of 1.7 ml/ minute, separation and quantitation are achieved. p-Dimethyl-aminobenzaldehyde may be used as an internal standard to compensate for variations in injection technique and instrumental conditions. With a 254 nm ultraviolet absorbance detector, 0.01 ug of calcitriol may be detected (3). [Pg.96]


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