Dynamic covalent hydrazine chemistry as a selective extraction and cleanup technique for the quantification of the Fusarium mycotoxin zearalenone in edible oils

Journal of Chromatography A

Volumn 1217, Issue 15, 2010, Pages 2206-2215

  Siegel, David ^a   Andrae, Karsten ^b   Proske, Matthias ^a   Kochan, Cindy ^a   Koch, Matthias ^a   Weber, Marcus ^b   Nehls, Irene ^a  

^a BAM FEDERAL INSTITUTE FOR MATERIALS RESEARCH AND TESTING   (Germany)

^b ZUSE INSTITUTE BERLIN   (Germany)

Author keywords

Dynamic covalent hydrazine chemistry; Edible oil; Extraction; HPLC FLD; Hydrazone; Hydrodynamic radius; Maize; SPE; Zearalenone

Indexed keywords

EDIBLE OIL; HPLC-FLD; HYDRAZONES; HYDRODYNAMIC RADIUS; SPE; ZEARALENONE;

AGRICULTURE; BUBBLES (IN FLUIDS); CHROMATOGRAPHIC ANALYSIS; CHROMATOGRAPHY; FLUID DYNAMICS; FUNCTIONAL POLYMERS; HYDRAZINE; HYDRODYNAMICS; LIQUIDS; MASS SPECTROMETRY; MOLECULAR STRUCTURE; NANOFILTRATION; OILS AND FATS; RESINS; SOLAR RADIATION; TOXIC MATERIALS;

HIGH PERFORMANCE LIQUID CHROMATOGRAPHY;

EDIBLE OIL; HYDRAZINE; RESIN; ZEARALENONE;

ACCURACY; ANALYTIC METHOD; ARTICLE; CHEMICAL ANALYSIS; CHEMICAL REACTION; CHEMICAL STRUCTURE; CONTROLLED STUDY; DYNAMIC COVALENT HYDRAZINE CHEMISTRY; FUSARIUM; GEL PERMEATION CHROMATOGRAPHY; HIGH PERFORMANCE LIQUID CHROMATOGRAPHY; HYDRODYNAMICS; HYDROGEN BOND; HYDROLYSIS; INTERMETHOD COMPARISON; MAIZE; NANOFILTRATION; NUT; OLIVE; PLANT SEED; PRIORITY JOURNAL; SIMULATION; TANDEM MASS SPECTROMETRY; VALIDITY;

ACIDS; CATALYSIS; CHROMATOGRAPHY, HIGH PRESSURE LIQUID; COMPUTER SIMULATION; FUSARIUM; HYDRAZINES; PLANT OILS; POLYMERS; REPRODUCIBILITY OF RESULTS; RESINS, SYNTHETIC; SOLVENTS; TIME FACTORS; WATER; ZEARALENONE;

FUSARIUM; OLEACEAE; ZEA MAYS;

EID: 77950690269     PISSN: 00219673     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.chroma.2010.02.019     Document Type: Article

References (47)

1. Zinedine A., Soriano J.M., Molto J.C., Manes J. Food Chem. Toxicol. 2007, 45:1.
2. Weidenbörner M. Encyclopedia of Food Mycotoxins 2001, Springer, Berlin.
3. Lauren D.R., Ringrose M.A. Food Addit. Contam. 1997, 14:435.
4. Schollenberger M., Muller H.M., Rufle M., Suchy S., Drochner W. Cereal Chem. 2008, 85:557.
5. European Commission Off. J. Eur. Union L 2006, 12:17.
6. European Commission Off. J. Eur. Union L 2007, 255:14.
7. WHO, Tech. Rep. Ser. 896 (2000) 93.
8. Krska R., Josephs R. Fresenius J. Anal. Chem. 2001, 369:469.
9. Abidi S.L. J. Chromatogr. A 2001, 935:173.
10. Moret S., Conte L.S. J. Chromatogr. A 2000, 882:245.
11. Gilbert-Lopez B., Garcia-Reyes J.F., Molina-Diaz A. Talanta 2009, 79:109.
12. Majerus P., Graf N., Krämer M. Mycotoxin Res. 2009, 25:117.
13. Schollenberger M., Muller H.M., Rufle M., Drochner W. Food Control 2008, 19:475.
14. Patel S., Hazel C.M., Winterton A.G.M., Mortby E. Food Addit. Contam. 1996, 13:833.
15. Dunne C., Meaney M., Smyth M., Tuinstra L. J. Chromatogr. 1993, 629:229.
16. Gottschalk C., Barthel J., Aulwum U., Engelhardt G., Bauer J., Meyer K. LC-GC North Am. 2009, 38.
17. Kappenstein O., Klaffke H., Mehlitz I., Tiebach R., Weber R., Lepschy J., Wittkowski R. Mycotoxin Res. 2005, 21:3.
18. Lanier C., Heutte N., Richard E., Bouchart V., Lebailly P., Garon D. J. Agric. Food Chem. 2009, 57:1640.
19. Jencks W.P. Prog. Phys. Org. Chem. 1964, 2:63.
20. Sayer J.M., Peskin M., Jencks W.P. J. Am. Chem. Soc. 1973, 95:4277.
21. Nguyen R., Huc I. Chem. Commun. 2003, 942.
22. Kalia J., Raines Ronald T. Angew. Chem. 2008, 120:7633.
23. Siegel D., Merkel S., Koch M., Nehls I. Food Chem. 2010, 120:902.
24. Siegel D., Rasenko T., Koch M., Nehls I. J. Chromatogr. A 2009, 1216:4582.
25. Rowan S.J., Cantrill S.J., Cousins G.R.L., Sanders J.K.M., Stoddart J.F. Angew. Chem. Int. Ed. 2002, 41:898.
26. Levrand B., Fieber W., Lehn J.M., Herrmann A. Helv. Chim. Acta 2007, 90:2281.
27. Levrand B., Ruff Y., Lehn J.M., Herrmann A. Chem. Commun. 2006, 2965.
28. Maeda T., Otsuka H., Takahara A. Prog. Polym. Sci. 2009, 34:581.
29. Ramstrom O., Lehn J.M. Nat. Rev. Drug Discov. 2002, 1:26.
30. Roe M.R., Xie H.W., Bandhakavi S., Griffin T.J. Anal. Chem. 2007, 79:3747.
31. Lindahl E., Hess B., van der Spoel D. J. Mol. Model. 2001, 7:306.
32. Bussi G., Donadio D., Parrinello M. J. Chem. Phys. 2007, 126:014101.
33. Schuttelkopf A.W., van Aalten D.M.F. Acta Crystallogr. D: Biol. Crystallogr. 2004, 60:1355.
34. Einstein A. Ann. Phys. 1905, 17:549560.
35. European Commission Off. J. Eur. Union L 2006, 70:12.
36. Gilbert J., Anklam E. Trends Anal. Chem. 2002, 21:468.
37. Brady O., Elsmie G. Analyst 1926, 51:77.
38. Bassette R., Day E.A. J. Am. Oil Chem. Soc. 1960, 37:482.
39. Keeney M. Anal. Chem. 1957, 29:1489.
40. Berthiller F., Schuhmacher R., Buttinger G., Krska R. J. Chromatogr. A 2005, 1062:209.
41. Maragou N.C., Rosenberg E., Thomaidis N.S., Koupparis M.A. J. Chromatogr. A 2008, 1202:47.
42. Ren Y., Zhang Y., Shao S., Cai Z., Feng L., Pan H., Wang Z. J. Chromatogr. A 2007, 1143:48.
43. Panneerselvam K., Rudiño-Piñera E., Soriano-García M. Acta Crystallogr. Sect. C: Cryst. Struct. Commun. 1996, 52:3095.
44. Miwa H. J. Chromatogr. A 2000, 881:365.
45. Peters R., Hellenbrand J., Mengerink Y., Van der Wal S. J. Chromatogr. A 2004, 1031:35.
46. van Leeuwen S.M., Hendriksen L., Karst U. J. Chromatogr. A 2004, 1058:107.
47. Brady O.L. J. Chem. Soc. 1931, 1:756.