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Abstrakty
This study aimed to optimize and validate methods for the analysis of thiamin and folic acid in fortified rice, pure and mixed to the milled rice (raw and cooked). The analysis was performed by high-performance liquid chromatography coupled to a diode array detector (HPLC—DAD). Different mobile phases were tested. Different ratios of organic modifier, pH ranges, triethylamine concentrations, and flow rates were used. For the validation, tests of recovery, repeatability, linearity, limit of detection (LOD), and limit of quantification (LOQ) were performed. The optimized methods showed good resolution of vitamins’ peaks, excellent recovery (82.6 to 104%), repeatability with relative standard deviation of peak areas, and retention times less than 10% and high coefficients of determination (0.9998 for thiamin and 0.9997 for folic acid). The LOD and LOQ were 0.00193 μg and 0.0193 μg for thiamin and 0.000934 μg and 0.00934 μg for folic acid. The optimized methods demonstrated reliability and sensitivity in the detection and quantification of these vitamins in fortified rice, pure and mixed to milled rice (raw and cooked). Furthermore, the methods were performed in isocratic mode, with short run time (<13 min), reflecting positively on the economy of reagents and analysis times.
Słowa kluczowe
Czasopismo
Rocznik
Tom
Strony
455--472
Opis fizyczny
Bibliogr. 29 poz., rys., tab.
Twórcy
autor
- Laboratory of Vitamin Analysis, Department of Nutrition and Health, Federal University of Viçosa, Avenida Ph Holfs, s/n, Campus Universitário, Viçosa, Minas Gerais, CEP: 36570-000, Brazil
autor
- Laboratory of Vitamin Analysis, Department of Nutrition and Health, Federal University of Viçosa, Avenida Ph Holfs, s/n, Campus Universitário, Viçosa, Minas Gerais, CEP: 36570 000, Brazil
autor
- Department of Food Technology, Federal University of Viçosa, Avenida Ph Holfs, s/n, Campus Universitário, Viçosa, Minas Gerais, CEP: 36571-000, Brazil
autor
- Laboratory of Vitamin Analysis, Department of Nutrition and Health, Federal University of Viçosa, Avenida Ph Holfs, s/n, Campus Universitário, Viçosa, Minas Gerais, CEP: 36570-000 , Brazil
autor
- Laboratory of Vitamin Analysis, Department of Nutrition and Health, Federal University of Viçosa, Avenida Ph Holfs, s/n, Campus Universitário, Viçosa, Minas Gerais, CEP: 36570 000, Brazil
Bibliografia
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- [2] FAO, Statistical Databases, http://faostat.fao.org/site/339/default.aspx, 2012
- [3] M. Walter, E. Marchezan II, and A. Avila, Ciênc. Rur, 38, 1184–1192 (2008)
- [4] N.B. Piccoli, N. Grede, S. de Pee, A. Singhkumarwong, E. Roks, R. Moench- Pfanner, and M.W. Bloem, Food. Nutr. Bull., 33, 360–372 (2012)
- [5] C.M. Della Lucia, M.D.V. Tostes, C.M.M. Silveira, L.A. Bordalo, F.C. Rodrigues, H.M. Pinheiro-Sant’Ans, H.S.D. Martino, and N.M.B. Costa, Arch. Latinoam. Nutr, 63, 64–73 (2013)
- [6] Y. Li, L.L. Diosady, S. Jankowski, Int. J. Food. Sci. Nutr., 59, 24–33 (2008)
- [7] C.M. Della Lucia, E.R. Silva, S.M.R. Ribeiro, H.M. Pinheiro-Sant’Ana, and S.C.C. Brandão, Q. Nov, 34, 335–340 (2011)
- [8] H.K. Trang, All Theses, http://www.http://tigerprints.clemson.edu/cgi/ view content.cgi?article=2745&context=all_theses, 2013
- [9] P.L.M. Lynch and I.S. Young, J. Chromatogr. A, 881, 267–284 (2000)
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- [13] R.R. Eitenmiller, L. Ye, and W.O. Landen, Vitamin Analysis for the Health and Food Science, Boca Raton, New York, 2008, pp. 291–318
- [14] K. Swan-Choo and T. E-Siong, Malays. J. Nutr., 2, 49–65 (1996)
- [15] G.F.M. Ball, Vitamins in Foods: Analysis, Bioavailability, and Stability, Boca Raton, New York, 2006, p. 651
- [16] M.W. Dong, J. Lepore, and T. Tarumoto, J. Chromatogr., 442, 81–95 (1988)
- [17] F.M. Lanças, Validação de Métodos Cromatográficos de Análise, São Carlos, 2004
- [18] R.R. Catharino, H.T. Godoy, and J.A. Lima-Pallone, Q. Nov, 29, 972–976 (2006)
- [19] S. A. S. Institute Inc., SAS/STAT User’s Guide, SAS Institute Inc., Cary, NC, 2003
- [20] PATH, Ultra Rice Technology, http://www.path.org/files/UltraRiceBrochure2000-web.pdf, 2011
- [21] R. San José Rodriguez, V. Fernández-Ruiz, M. Cámara, and M.C. Sánchez-Mata, J. Cereal. Sci., 55, 293–299 (2012)
- [22] S. Albalfi-Hurtado, M.T. Veciana-Nogués, M. Izquierdo-Pulido, and A. Mariné-Font, J. Chromatogr. A, 778, 247–253 (1997)
- [23] B. Hucker, L. Wakeling, and F. Vriesekoop, J. Cereal. Sci., 56, 300–306 (2012)
- [24] A.E.F. Presoto and L.B.D. Almeida-Muradian, Q. Nov, 31, 498–502 (2008)
- [25] T.R. Boen, B.T. Soeiro, E.R. Pereira-Filho, and J.A. Lima-Pallone, J. Braz. Chem. Soc., 19, 53–59 (2008)
- [26] A. Lebiedziñska, M. Dbrowska, P. Szefer, and M. Marszall, Toxicol. Mech. Methods, 18, 463–467 (2008)
- [27] J. Alaburda, A.P. de Almeida, L. Shundo, V. Ruvieri, and M. Sabino, J. Food. Comp. Anal., 21, 336–342 (2008)
- [28] AOAC, Peer Verified Methods Program, Manual on Policies and Procedures AOAC International, Arlington, 1993
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Uwagi
PL
Opracowanie ze środków MNiSW w ramach umowy 812/P-DUN/2016 na działalność upowszechniającą naukę.
Typ dokumentu
Bibliografia
Identyfikator YADDA
bwmeta1.element.baztech-84c679b5-9014-484a-8cb6-6425daf66758