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Quantification of lutein in dietary supplements by reversed-phase high-performance thin-layer chromatography with visible-mode densitometry

Identyfikatory
Warianty tytułu
Języki publikacji
EN
Abstrakty
EN
A quantitative method, using chemically bonded C18 silica gel HPTLC plates, automated band-wise sample application, and automated visible-mode densitometry, has been developed for the determination of the carotenoid pigment lutein in nutrition supplements consumed to reduce the risk of macular degeneration. Three products containing 20 mg or 6 mg of lutein as the free alcohol or dipalmitate ester plus other ingredients were analyzed. Comparison with a lutein reference standard revealed that recoveries ranged from 112 to 247% relative to the stated label value. Accuracy was validated by analysis of a spiked blank and a second certified lutein standard, and precision by performing replicate analysis. Accuracy was found to be within 0.1% and 0.4% of theoretical values, and precision was 1.59% relative standard deviation.
Słowa kluczowe
Rocznik
Tom
Strony
151--158
Opis fizyczny
Bibliogr. 16 poz., tab.
Twórcy
autor
  • Department of Chemistry, Lafayette College, Easton, PA 18042, USA
autor
  • Department of Chemistry, Lafayette College, Easton, PA 18042, USA
autor
  • Department of Chemistry, Lafayette College, Easton, PA 18042, USA
Bibliografia
  • [1] H. H. Strain and J. Sherma, J. Chem. Educ., 46, 476 (1969)
  • [2] C. J. Marsit, B. Fried, and J. Sherma, J. Parasitol., 86, 635 (2000)
  • [3] P. S. Hamano and A. Z. Mercadante, J. Food Comp. Anal., 14, 335 (2001)
  • [4] Food and Beverage Division of the Perkin-Elmer Corporation, Food Testing and Analysis, August/September, 37 (1999)
  • [5] J. Sherma, J. AOAC Int., 77, 297 (1994)
  • [6] J. J. Negro and J. Garrido-Fernandez, Comp. Biochem. Phys. B, 126, 347 (2000)
  • [7] B. Czeczuga, H. Kilias, E. Czeczuga-Semeniuk, L. E. Muhr, H. T. Lumbsch, and G. Hestmark, J. Hattori Bot. Lab., 89, 299 (2000)
  • [8] T. Hodison, C. Socaciu, I. Ropan, and G. Neamtu, J. Pharmaceut. Biomed., 16, 521 (1997)
  • [9] J. G. Fernandez, B. G. Rojas, L. G. Guerrero, and M. Mosquera, Grasas Aceites, 41, 404 (1990)
  • [10] J. Sherma and M. Ervin, J. Liq. Chromatogr., 9, 3423 (1986)
  • [11] S. D. Wagner, S. W. Kaufer, and J. Sherma, J. Liq. Chromatogr. Related Technol., 24, 2525 (2001)
  • [12] J. Pachuski and J. Sherma, J. Liq. Chromatogr. Related Technol., in press
  • [13] J. Sherma, C. M. O’Hea, and B. Fried, J. Planar Chromatogr., 5, 343, 1992
  • [14] The United States Pharmacopeia/National Formulary (USP 24/NF 19), United States Pharmacopeial Convention, Inc., Rockville, MD, USA, 2000
  • [15] D. DiGregorio, E. Westgate, and J. Sherma, Acta Chromatogr., 10, 190 (2000)
  • [16] K. Ferenczi-Fodor, Z. Vegh, A. Nagy-Turak, B. Renger, and M. Zeller, J. AOAC Int., 84, 1265 (2001)
Typ dokumentu
Bibliografia
Identyfikator YADDA
bwmeta1.element.baztech-article-BAT3-0026-0032
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