Literature DB >> 16742460

A gas-liquid-chromatographic procedure for separating a wide range of metabolites occuring in urine or tissue extracts.

C E Dalgliesh1, E C Horning, M G Horning, K L Knox, K Yarger.   

Abstract

1. A gas-liquid-chromatographic procedure is described which permits separation and identification on the same chromatogram of a wide range of substances occurring in urine or tissue extracts. The method uses hydrogen flame ionization, which detects organic compounds whether free or conjugated with no requirement for specific reactive groups. 2. For chromatography, carboxyl groups are quantitatively converted into methyl esters or trimethylsilyl esters. Phenolic, alcoholic and potential enolic groups are converted into trimethylsilyl ethers. Separations are carried out on a 6ft. column of either 10% F-60 (a polysiloxane) or 1% F-60, temperature programming at 2 degrees /min. being used over such part of the temperature range 30 degrees -260 degrees as is required. Propionyl derivatives of hydroxy compounds can also be used, but only on a non-quantitative basis. Derivatives and columns have been selected for optimum range of usefulness when large numbers of samples are examined by using automated gas chromatography. 3. The method is applicable to: fatty acids above butyric acid; di- and tri-carboxylic acids; hydroxy acids and keto acids; polyhydroxy and alicyclic compounds such as glycerol, inositol, quinic acid, shikimic acid, ascorbic acid and sugar alcohols; aromatic hydroxy and acidic compounds, both benzenoid and indolic; sesquiterpenes; steroids; glycine conjugates; mercapturic acids; glucuronides. It is not satisfactory for sulphate conjugates, iminazoles or polypeptides. 4. Methylene units provide an accurate and reproducible parameter for characterizing peak position. Methylene unit values are reported for a large variety of substances occurring in, or related to those occurring in, urine and tissue extracts. 5. The nature of derivatives was confirmed by combining gas chromatography with mass spectrometry. Combined gas chromatography-mass spectrometry gives a diagnostic tool of great power in the evaluation of metabolic patterns, and various uses are discussed.

Entities:  

Year:  1966        PMID: 16742460      PMCID: PMC1270188          DOI: 10.1042/bj1010792

Source DB:  PubMed          Journal:  Biochem J        ISSN: 0264-6021            Impact factor:   3.857


  7 in total

Review 1.  SEPARATION AND DETERMINATION OF STEROIDS BY GAS CHROMATOGRAPHY.

Authors:  E C HORNING; W J VANDENHEUVEL; B G CREECH
Journal:  Methods Biochem Anal       Date:  1963

2.  IDENTIFICATION AND QUANTIFICATION OF NEUTRAL FECAL STEROIDS BY GAS-LIQUID CHROMATOGRAPHY AND MASS SPECTROMETRY: STUDIES OF HUMAN EXCRETION DURING TWO DIETARY REGIMENS.

Authors:  P ENEROTH; K HELLSTROEM; R RYHAGE
Journal:  J Lipid Res       Date:  1964-04       Impact factor: 5.922

3.  Microanalytical determination of dihydroxy aromatic acids by gas chromatography.

Authors:  C M WILLIAMS; R H LEONARD
Journal:  Anal Biochem       Date:  1963-04       Impact factor: 3.365

4.  Quantitative analysis of fecal bile acids by gas-liquid chromatography.

Authors:  M MAKITA; W W WELLS
Journal:  Anal Biochem       Date:  1963-06       Impact factor: 3.365

5.  Gas chromatography of the dihydroxybenzoic acids.

Authors:  C M Williams
Journal:  Anal Biochem       Date:  1965-05       Impact factor: 3.365

6.  [Analysis of steroids by gas phase chromatography].

Authors:  W J Van den Heuvel; E C Horning
Journal:  Bull Soc Chim Biol (Paris)       Date:  1965

7.  Separation and identification of derivatives of biologic amines by gas-liquid chromatography.

Authors:  P Capella; E C Horning
Journal:  Anal Chem       Date:  1966-02       Impact factor: 6.986

  7 in total
  29 in total

1.  Human exposure to styrene. I. The gaschromatographic determination of urinary phenylglyoxylic acid using diazomethane derivatization.

Authors:  D Bauer; M Guillemin
Journal:  Int Arch Occup Environ Health       Date:  1976-04-28       Impact factor: 3.015

Review 2.  Metabolomics: moving to the clinic.

Authors:  Anders Nordström; Rolf Lewensohn
Journal:  J Neuroimmune Pharmacol       Date:  2009-04-28       Impact factor: 4.147

Review 3.  Biochemical individuality reflected in chromatographic, electrophoretic and mass-spectrometric profiles.

Authors:  Milos V Novotny; Helena A Soini; Yehia Mechref
Journal:  J Chromatogr B Analyt Technol Biomed Life Sci       Date:  2008-04-15       Impact factor: 3.205

Review 4.  Development of capillary liquid chromatography: A personal perspective.

Authors:  Milos V Novotny
Journal:  J Chromatogr A       Date:  2017-06-24       Impact factor: 4.759

Review 5.  Illuminating the dark metabolome to advance the molecular characterisation of biological systems.

Authors:  Oliver A H Jones
Journal:  Metabolomics       Date:  2018-07-19       Impact factor: 4.290

Review 6.  Innovation: Metabolomics: the apogee of the omics trilogy.

Authors:  Gary J Patti; Oscar Yanes; Gary Siuzdak
Journal:  Nat Rev Mol Cell Biol       Date:  2012-03-22       Impact factor: 94.444

7.  Effect of trans fatty acids on plasma lipids, platelet function and systolic blood pressure in stroke-prone spontaneously hypertensive rats.

Authors:  M T Chiang; M I Otomo; H Itoh; Y Furukawa; S Kimura; H Fujimoto
Journal:  Lipids       Date:  1991-01       Impact factor: 1.880

8.  Analysis of renal cell carcinoma as a first step for developing mass spectrometry-based diagnostics.

Authors:  Kentaro Yoshimura; Lee Chuin Chen; Mridul Kanti Mandal; Tadao Nakazawa; Zhan Yu; Takahito Uchiyama; Hirokazu Hori; Kunio Tanabe; Takeo Kubota; Hideki Fujii; Ryohei Katoh; Kenzo Hiraoka; Sen Takeda
Journal:  J Am Soc Mass Spectrom       Date:  2012-07-31       Impact factor: 3.109

9.  The metabolism of orally administered L-Dopa in Parkinsonism.

Authors:  D B Calne; F Karoum; C R Ruthven; M Sandler
Journal:  Br J Pharmacol       Date:  1969-09       Impact factor: 8.739

10.  Microbial metabolism of pyridinium compounds. Metabolism of 4-carboxy-1-methylpyridinium chloride, a photolytic product of paraquat.

Authors:  K A Wright; R B Cain
Journal:  Biochem J       Date:  1972-07       Impact factor: 3.857

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