Determination of thyreostatics in animal feed by micellar electrokinetic chromatography

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Josep Esteve-Romero, Ima Escrig-Tena, Ernesto F. Simó-Alfonso and Guillermo Ramis-Ramos


Abstract

The determination of the thyreostatics 2-thiouracil, its derivatives (4-methyl-2-thiouracil, 4-propyl-2-thiouracil and 4-phenyl-2-thiouracil) and methimazole in manufactured dried animal feed by micellar electrokinetic chromatography (MEKC) is described. A 99 ± 5% extraction yield at the 20 µg g–1 level (n = 8) was achieved by shaking the milled fodder with methanol–1 M NaOH (80 + 20). Aliquots of the supernatant were injected in a 75 µm × 33.5 cm uncoated silica capillary using pressure; separation was performed at 23 °C with 15 kV (positive polarity) in a background electrolyte (BGE) containing 40 mM sodium dihydrogenphosphate, 50 mM sodium dodecyl sulfate and 15 mM Tween 20 at pH 9. When the surfactants were added to the BGE, all the thyreostatics were well resolved and the fodder extracts showed lower backgrounds. The peaks appeared within the 2.25–5.2 min range with efficiencies in the 2.5 × 104–8 × 104 range; methimazole appeared in the vicinity of the electroosmotic migration time. Calibration curves were linear within the studied range (20–200 µg ml–1, r2 > 0.998). Limits of detection in the extracts of spiked fodder samples ranged from 0.25 to 0.4 µg ml–1, which corresponded to 0.6–1.0 µg of drug per gram of fodder. Peak area repeatabilities were about 4% at the 20 µg ml–1 level.


References

  1. A. Burger, in Burger' Medicinal Chemistry, 3rd edn., Wiley, New York, 1970, part II, p. 853 Search PubMed.
  2. M. G. El-Bardicy, Y. S. El-Saharty and M. S. Tawakkol, Talanta, 1993, 40, 577 CrossRef CAS.
  3. I. López García, P. Viñas and J. A. Martínez Gil, Fresenius' J. Anal. Chem., 1993, 345, 723 CrossRef.
  4. M. G. El-Bardicy, Y. S. El-Saharty and M. S. Tawakkol, Spectrosc. Lett., 1991, 24, 1079 CAS.
  5. C. S. P. Sastry, P. Satyanarayana, N. R. P. Singh and A. R. M. Rao, J. Inst. Chem., 1988, 60, 162 Search PubMed.
  6. S. M. Sultan, J. Pharm. Biomed. Anal., 1992, 10, 1059 CrossRef CAS.
  7. M. S. García, M. I. Albero, C. Sánchez Pedreño and L. Tobal, Analyst, 1995, 120, 129 RSC.
  8. H. Y. Aboul-Enein, J. Pharm. Pharmacol, 1979, 31, 196 Search PubMed.
  9. A. Berka, K. Velasevic and K. Nikolic, Pharmazie, 1989, 44, 499 Search PubMed.
  10. K. Nikolic and K. Velasevic, Pharmazie, 1987, 42, 689 Search PubMed.
  11. M. B. Thomas and T. A. Last, Anal. Chem., 1988, 60, 2158 CrossRef CAS.
  12. G. R. Cannell, J. P. Williams, A. S. Yap and R. H. Mortimer, J. Chromatogr. A, 1991, 564, 310 CrossRef CAS.
  13. H. F. De Brabander, P. Batjoens and J. Van Hoff, J. Planar Chromatogr. Mod. TLC, 1992, 5, 124 Search PubMed.
  14. Th. Reuvers De Lange, Institute of Health Carlos III, Centro Nacional de Alimentación, Ministerio de Sanidad y Consumo, Madrid (Spain),Method 7.1.
  15. D. G. Watson, C. D. Bates, G. G. Skellern, R. Mairs and S. Martin, Rapid Commun. Mass Spectrom., 1991, 5, 141 CAS.
  16. R. Schilt, J. M. Weseman, H. Hooijerink, H. J. Korbee and W. A. Traag, J. Chromatogr., Biomed. Appl., 1989, 81, 127 CrossRef CAS.
  17. Th. Reuvers De Lange, R. Díaz Díaz, J. Gómez Herrero, Institute of Health Carlos III, Centro Nacional de Alimentación, Ministerio de Sanidad y Consumo, Madrid (Spain), Method 7.2.
  18. R. Halpern, D. S. Cooper, J. D. Kieffer, V. Saxe, H. Mover, F. Mallof and E. C. Ridgway, Endocrinology, 1983, 113, 915 Search PubMed.
  19. L. Krivánková, S. Krásensky and P. Boček, Electrophoresis, 1996, 17, 1959 CAS.
  20. Veevoeders en Dieren Specialiteiten, http://users.skynet.be/vds/gen-e.htm.
  21. M. J. Adams, Chemometrics in Analytical Spectroscopy, Royal Society of Chemistry, Cambridge, 1995, pp. 32–34 Search PubMed.
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