Identification of glycerophospholipids in rapeseed, olive, almond, and sunflower oils by LC–MS and LC–MS–MS

2004 ◽  
Vol 82 (7) ◽  
pp. 1210-1215 ◽  
Author(s):  
Sadok Boukhchina ◽  
Khaled Sebai ◽  
Ammar Cherif ◽  
Habib Kallel ◽  
Paul M Mayer

HPLC employing a thermostatted Lichrospher 100 diol column was used to separate mixtures of glycerophospholipids of rapeseed, olive, almond, and sunflower oils. Elution was performed with a binary gradient of two mixed solvents A: hexane – isopropanol – acetic acid – triethylamine (82:17:1.0:0.08 v/v/v/v) and B: isopropanol – water – acetic acid – triethylamine (85:14:1.0:0.08 v/v/v/v). The LC effluent was directly introduced into the mass spectrometer through an electrospray capillary. Information about the fatty acid composition of each glycerophos pho lipid class was given by tandem mass spectrometry (MS–MS). These techniques permitted a rapid separation and identification of complex mixtures of glycerophospholipids. The relative abundance of each lipid class in each oil was also determined. The resulting glycerophospholipid signature may provide an efficient means of identifying oil origin and possible adulteration.Key words: glycerophospholipids, vegetable oils, tandem mass spectrometry, LC–MS.

2005 ◽  
Vol 51 (8) ◽  
pp. 1487-1492 ◽  
Author(s):  
Henkjan Gellekink ◽  
Dinny van Oppenraaij-Emmerzaal ◽  
Arno van Rooij ◽  
Eduard A Struys ◽  
Martin den Heijer ◽  
...  

Abstract Background: It has been postulated that changes in S-adenosylhomocysteine (AdoHcy), a potent inhibitor of transmethylation, provide a mechanism by which increased homocysteine causes its detrimental effects. We aimed to develop a rapid and sensitive method to measure AdoHcy and its precursor S-adenosylmethionine (AdoMet). Methods: We used stable-isotope dilution liquid chromatography–electrospray injection tandem mass spectrometry (LC-ESI-MS/MS) to measure AdoMet and AdoHcy in plasma. Acetic acid was added to prevent AdoMet degradation. Solid-phase extraction (SPE) columns containing phenylboronic acid were used to bind AdoMet, AdoHcy, and their internal standards and for sample cleanup. An HPLC C18 column directly coupled to the LC-MS/MS was used for separation and detection. Results: In plasma samples, the interassay CVs for AdoMet and AdoHcy were 3.9% and 8.3%, and the intraassay CVs were 4.2% and 6.7%, respectively. Mean recoveries were 94.5% for AdoMet and 96.8% for AdoHcy. The quantification limits were 2.0 and 1.0 nmol/L for AdoMet and AdoHcy, respectively. Immediate acidification of the plasma samples with acetic acid prevented the observed AdoMet degradation. In a group of controls (mean plasma total Hcy, 11.2 μmol/L), plasma AdoMet and AdoHcy were 94.5 and 12.3 nmol/L, respectively. Conclusions: Stable-isotope dilution LC-ESI-MS/MS allows sensitive and rapid measurement of AdoMet and AdoHcy. The SPE columns enable simple cleanup, and no metabolite derivatization is needed. The instability of AdoMet is a serious problem and can be prevented easily by immediate acidification of samples.


2015 ◽  
Vol 7 (7) ◽  
pp. 2950-2958 ◽  
Author(s):  
Lauren Mullin ◽  
Jennifer A. Burgess ◽  
Ingrid Ericson Jogsten ◽  
Dawei Geng ◽  
Andy Aubin ◽  
...  

Analysis of the brominated flame retardant hexabromocyclododecane (HBCDD) is characterized by the separation of its three predominant diastereomers.


1989 ◽  
Vol 24 (10) ◽  
pp. 946-952 ◽  
Author(s):  
Joachim Stach ◽  
Dieter Zimmer ◽  
Monika MÖDer And ◽  
Rainer Herzschuh

Author(s):  
Anthony T. Jackson ◽  
Richard C. K. Jennings ◽  
James H. Scrivens ◽  
Martin R. Green ◽  
Robert H. Bateman

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