Determination of Ergot Alkaloids

1960 ◽  
Vol 43 (2) ◽  
pp. 224-229
Author(s):  
Thomas G Alexander
Keyword(s):  
2017 ◽  
Vol 10 (1) ◽  
pp. 5-29 ◽  
Author(s):  
F. Berthiller ◽  
C. Brera ◽  
M.H. Iha ◽  
R. Krska ◽  
V.M.T. Lattanzio ◽  
...  

This review summarises developments in the determination of mycotoxins over a period between mid-2015 and mid-2016. Analytical methods to determine aflatoxins, Alternaria toxins, ergot alkaloids, fumonisins, ochratoxins, patulin, trichothecenes and zearalenone are covered in individual sections. Advances in proper sampling strategies are discussed in a dedicated section, as are methods used to analyse botanicals and spices and newly developed liquid chromatography mass spectrometry based multi-mycotoxin methods. This critical review aims to briefly discuss the most important recent developments and trends in mycotoxin determination as well as to address limitations of presented methodologies.


1986 ◽  
Vol 69 (4) ◽  
pp. 697-699
Author(s):  
George M Ware ◽  
Allen S Carman ◽  
Octave J Francis ◽  
Shia S Kuan

Abstract A method is described for the determination of individual ergot alkaloids in wheat. The sample is extracted with ethyl acetate-4% ammonium hydroxide (100 + 10), and the extract is cleaned up by liquidliquid partition. The ergot alkaloids are resolved by liquid chromatography (LC), using a porous cross-linked polystyrene-divinylbenzene resin column and a mobile phase consisting of acetonitrile-0.05M dibasic ammonium phosphate (55 + 45) buffered at pH 10.0. The ergot alkaloids ergonovine, ergonovinine, ergotamine, ergotaminine, α-ergocryptine, α-ergocryptinine, ergocristine, and ergocristinine are separated by LC and detected with a fluorescence detector. Recovery of ergot alkaloids added to wheat at levels of 16-760 ng/g averaged 85.6% with a coefficient of variation of 11.1%.


1985 ◽  
Vol 4 (6) ◽  
pp. 601-607 ◽  
Author(s):  
M. Žorž ◽  
J. Culig ◽  
Z. Kopitar ◽  
D. Milivojevic ◽  
A. Marušič ◽  
...  

1 Ergot alkaloids and their dihydrogenated methanesulphonate (ms) salts were determined and measured in human plasma. 2 High-performance liquid chromatography (HPLC) with fluorometric detection was used for separation of ergot alkaloids in plasma. 3 Several ergot alkaloids and their derivatives, including lysergide (LSD), can be identified in cases of poisoning.


2008 ◽  
Vol 391 (2) ◽  
pp. 563-576 ◽  
Author(s):  
Rudolf Krska ◽  
George Stubbings ◽  
Roy Macarthur ◽  
Colin Crews

2016 ◽  
Vol 408 (12) ◽  
pp. 3093-3102 ◽  
Author(s):  
Julia Nowak ◽  
Michał Woźniakiewicz ◽  
Piotr Klepacki ◽  
Anna Sowa ◽  
Paweł Kościelniak

1996 ◽  
Vol 755 (2) ◽  
pp. 251-259 ◽  
Author(s):  
Benno A. Ingelse ◽  
Mirko Flieger ◽  
Henk A. Claessens ◽  
Frans M. Everaerts

1977 ◽  
Vol 10 (3) ◽  
pp. 147-150 ◽  
Author(s):  
M. Prošek ◽  
E. Kučan ◽  
M. Katić ◽  
M. Bano
Keyword(s):  

2013 ◽  
Vol 6 (2) ◽  
pp. 105-115 ◽  
Author(s):  
S.V. Malysheva ◽  
J. Diana Di Mavungu ◽  
E. Schoeters ◽  
D.A. Larionova ◽  
I.Y. Goryacheva ◽  
...  

A rapid liquid chromatography-tandem mass spectrometric (LC-MS/MS) method was developed for the determination of ergot alkaloids in buffered solutions from in vitro studies. The method implied a liquid-liquid extraction of the analytes under alkaline conditions prior to LC-MS/MS analysis and resulted in good recovery (91-123%) of the six ergot alkaloids defined by the European Food Safety Authority as most important, namely ergometrine, ergosine, ergotamine, ergocornine, ergokryptine and ergocristine, as well as their corresponding epimers. The method also proved to be sensitive, repeatable, linear, accurate and robust. Furthermore, the method was applied to evaluate the in vitro binding efficacy of a clay-based mycotoxin binder towards ergometrine, ergosine and ergocornine, through a design encompassing pH 3.0 and 6.8 to mimic the digestive tract. The binder demonstrated binding efficacy of 24, 93 and 97%, respectively, for these ergot alkaloids.


Molecules ◽  
2021 ◽  
Vol 26 (12) ◽  
pp. 3717
Author(s):  
Laura Carbonell-Rozas ◽  
Laura Gámiz-Gracia ◽  
Francisco J. Lara ◽  
Ana M. García-Campaña

An ultra-high performance liquid chromatography coupled to tandem mass spectrometry method is proposed for the determination of the major ergot alkaloids (ergometrine, ergosine, ergotamine, ergocornine, ergokryptine, ergocristine) and their epimers (ergometrinine, ergosinine, ergotaminine, ergocorninine, ergokryptinine, and ergocristinine) in oat-based foods and food supplements. A modified QuEChERS (quick, easy, cheap, effective, rugged, and safe) procedure was applied as sample treatment, reducing the consumption of organic solvent and increasing sensitivity. This method involved an extraction with acetonitrile and ammonium carbonate (85:15, v/v) and a clean-up step based on dispersive solid-phase extraction, employing a mixture of C18/Z-Sep+ as sorbents. Procedural calibration curves were established and limits of quantification were below 3.2 μg/kg for the studied compounds. Repeatability and intermediate precision (expressed as RSD%) were lower than 6.3% and 15%, respectively, with recoveries ranging between 89.7% and 109%. The method was applied to oat-based products (bran, flakes, flour, grass, hydroalcoholic extracts, juices, and tablets), finding a positive sample of oat bran contaminated with ergometrine, ergosine, ergometrinine, and ergosinine (total content of 10.7 μg/kg).


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