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Validated method to determine (±)-gossypol in Candida tropicalis culture by high-performance liquid chromatography

Identyfikatory
Warianty tytułu
Języki publikacji
EN
Abstrakty
EN
A validated high-performance liquid chromatography (HPLC) method has been developed to analyze the (±)-gossypol in the selection of strains of Candida tropicalis culture. Since gossypol was easily degraded and oxidized, the addition of antioxidant NADPH-Na4 and acetone extraction was chosen to prevent gossypol degradation and gradient elution assay was applied to obtain gossypol resolution. Concentrations of gossypol in C. tropicalis ZD-3 culture 20 μg/mL were determined, and concentration–time profiles were observed. Linearity of the gossypol standard curve by HPLC area method was ranged from 0.1 to 20 μg/mL with Y = 26.954 × X − 29.547, R2 = 0.9991, and n = 3, with limit of detection (LOD) of 50 ng/mL and lower limit of quantification (LLOQ) of 500 ng/mL. The recovery rate is dose-dependent and ranged from 85.3% to 103.5%. It is a rapid and reliable HPLC method for gossypol quantization in microorganism culture which could be applied in solid fermentation in the feed industry.
Rocznik
Strony
269--273
Opis fizyczny
Bibliogr. 18 poz., rys.
Twórcy
autor
  • College of Animal Science and Technology, Shihezi University, Shihezi, Xinjiang 832000, P.R. China
autor
  • College of Animal Science and Technology, Shihezi University, Shihezi, Xinjiang 832000, P.R. China
autor
  • College of Animal Science and Technology, Shihezi University, Shihezi, Xinjiang 832000, P.R. China
  • College of Animal Science and Technology, Shihezi University, Shihezi, Xinjiang 832000, P.R. China
autor
  • College of Animal Science and Technology, Shihezi University, Shihezi, Xinjiang 832000, P.R. China
autor
  • College of Animal Science and Technology, Shihezi University, Shihezi, Xinjiang 832000, P.R. China
autor
  • College of Animal Science and Technology, Shihezi University, Shihezi, Xinjiang 832000, P.R. China
Bibliografia
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  • [4] Zhang W. J.; Xu Z. R.; Zhao S. H.; Jiang J. F.; Wang Y. B.; Yan X. H. Toxicon 2006, 48, 221–226.
  • [5] Zhang W. J.; Xu Z. R.; Sun J. Y.; Yang X. J. Zhejiang Univ.-Sci. B 2006, 7, 690–695.
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  • [7] Nazarova I. P.; Nezhinskaya G. A.; Glushenkova A. I.; Umarov A. U. Chem. Nat. Compd. 1979, 15, 530–533.
  • [8] Nomeir A. A.; Abou-Donia M. B. J. Am. Oil Chem. Soc. 1982, 59, 546–549.
  • [9] Coward L.; Gorman G.; Noker P.; Kerstner-Wood C.; Pellecchia M.; Reed J. C.; Jia L. J. Pharmaceut. Biomed. 2006, 42, 581–586.
  • [10] Lee K. J.; Dabrowski K. J. Chromatogr. B 2002, 779, 313.
  • [11] Lin H.; Gounder M. K.; Bertino J. R.; Kong A. N. T.; Dipaola R. S.; Stein M. N. J. Pharmaceut. Biomed. 2012, 66, 371.
  • [12] Lee K. J.; Dabrowski K. J. Agr. Food Chem. 2002, 50, 3056.
  • [13] Hron Sr R. J.; Kim H. L.; Calhoun M. C.; Fisher G. S. J. Am. Oil Chem. Soc. 1999, 76, 1351–1355.
  • [14] Chamkasem N. J. Am. Oil Chem. Soc. 1988, 65, 1601–1604.
  • [15] Vshivkov S.; Pshenichnov E.; Golubenko Z.; Akhunov A.; Namazov S.; Stipanovic R. D. J. Chromatogr. B: Anal. Technol. Biomed. Life Sci. 2012, 908, 94–97.
  • [16] Jefford C. W.; Grant H. G. Anal. Chim. Acta 1985, 166, 311–314.
  • [17] Jia L.; Coward L. C.; Kerstnerwood C. D.; Cork R. L.; Gorman G. S.; Noker P. E.; Kitada S.; PellecchiaM.; ReedJ. C. Cancer Chemother. Pharmacol. 2008, 61, 63–73.
  • [18] Krempl C.; Heidel-Fischer H. M.; Jiménez-Alemán G. H.; ReicheltM.; MenezesR. C.; Boland W.; Vogel H.; Heckel D. G.; JoußenN. Insect. Biochem. Molec. 2016, 78, 69–77.
Uwagi
PL
Opracowanie rekordu w ramach umowy 509/P-DUN/2018 ze środków MNiSW przeznaczonych na działalność upowszechniającą naukę (2018).
Typ dokumentu
Bibliografia
Identyfikator YADDA
bwmeta1.element.baztech-98470163-0186-4636-b73f-14ed383c6e45
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