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Prostanoids analysis

Samples for prostanoid analysis by GC-MS must be carefully prepared and purified high-performance liquid chromatography is particularly useful in this respect (Frolich, 1977). Mass spectrometric quantification is achieved through the use of stable isotopes as internal standards, e.g. 3,3,4,4fH 4-PGF2 (Fisher and Frolich, 1982). Gas-chromatographic separation is improved with suitable capillary columns (Rigaud eta/., 1981). [Pg.437]

Cyclic diethylsilylene and di-tert.-butylsilylene derivatives have been used to protect diol groups in steroids and prostanoids [539-541]. N,0-bis(diethylhydrogensilyl)trifluoro-methylacetamide simultaneously converts Isolated hydroxyl groups to the diethyllu ogensilyl ether allowing a single step derivatization toVp used for the analysis of corticosteriods. [Pg.949]

Narumiya, S., and EitzGerald, G. A. (2001) Genetic and pharmacological analysis of prostanoid receptor function. J. Clin. Invest. 108, 25-30. [Pg.178]

Investigating metabolism or stability of prostanoids, radiolabeled precursors or analytes are often used. The tritiated or -labeled compounds can easily be detected without any further derivatization using online or off-line liquid scintillation, which is not impaired by any interferences derived from matrix components. Efficient but less sensitive PG analysis is possible by UV detection (190-210 nm) of underivatized substances demanding the remove of interfering contaminants or simple sample matrices like buffers or some cell supernatants. [Pg.1275]

Kapron, J. Wu, J. Mauriala, T. Clark, P. Purves, R.W. Bateman, K.P, Simultaneous analysis of prostanoids nsing liquid chromatography/high-field asymmetrie waveform ion mobility spectrometry/tandem mass spectrometry. Rapid Commun. Mass Spectrom. 2006, 20, 1504-1510. [Pg.212]

The presence of the TMS groups has little influence on fragmentation in the NICI mode [91,100,124], The hivourable GC-MS behaviour of the PFB—TMS and MO—PFB—TMS derivatives has made this the method of choice for the validation of other less specific assay techniques such as radioimmunoassay (RIA) [112, 117]. The GC—MS-MS behaviour of prostanoid ME—TMS, MO-ME-TMS [96-98, 1251 PFB-TMS and MO-PFB-TMS [116,125) derivatives has been investigated with a view to improving the selectivity of GC-MS analyses. Indications are that this approach is capable of achieving high sensitivities and selectivities in the analysis of prostanoids. [Pg.63]

Prostaglandins Isoprostanes and Synthetic Prostanoid Drugs Analysis by HPLC... [Pg.1920]

Nowadays, especially pharmaceutical applications make use of the highly selective and saisitive LC-MS/MS methods for both qualitative and quantitative analysis. Depending on the structure of the synthetic prostanoids, product ions of highest inteisity goierated by CID may be derived from larger ntm-natural substituents, e.g., 3-tiifluoromethylphenolate (from travoprost or fluprostenol, Rg. 3). ... [Pg.1925]

ANALYSIS OF PROSTANOIDS AND THEIR METABOLITES BY GAS CHROMATOGRAPHY-MASS SPECTROMETRY... [Pg.82]

The objective of this contribution is to discuss still another method for the analysis of the prostanoids and similar compounds (the eicosanoids")/ used by other investigators to a limited extent compared with the three assays mentioned above, namely gas chromatography with electron-capture detection (GC-EC). [Pg.156]


See other pages where Prostanoids analysis is mentioned: [Pg.440]    [Pg.440]    [Pg.167]    [Pg.652]    [Pg.653]    [Pg.46]    [Pg.60]    [Pg.84]    [Pg.26]    [Pg.26]    [Pg.61]    [Pg.61]    [Pg.79]    [Pg.88]    [Pg.89]    [Pg.440]    [Pg.189]    [Pg.1926]    [Pg.82]    [Pg.86]    [Pg.91]    [Pg.241]    [Pg.217]    [Pg.217]    [Pg.218]   
See also in sourсe #XX -- [ Pg.217 ]




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Prostanoids

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