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Gas chromatographic determination of parabens after in-situ derivatization and dispersive liquid-liquid microextraction

Identyfikatory
Warianty tytułu
Języki publikacji
EN
Abstrakty
EN
Dispersive liquid-liquid microextraction in combination with an in situ derivatization is suggested for parabens sampling and preconcentration. The derivatization was carried out with acetic anhydride under alkaline conditions maintained using di-potassium hydrogen phosphate. The effects of an extraction solvent type, extraction and disperser solvents volume, extraction time, and ionic strength of the solution on the extraction efficiency were investigated. Chlorobenzene containing n-hexadecane as internal standard was used as an extracting solvent and acetone was used as a disperser solvent. The calibration graphs were linear up to 10 mg mL-1, correlation coefficients were 0.997–0.999, enrichment factors were from 70 for methylparaben to 210 for butylparaben, and detection limits were 22, 4.2, 3.3, and 2.5 µg L−1 for methylparaben, ethylparaben, propylparaben, and butylparaben, respectively. Repeatabilities of the results were acceptable with relative standard deviations up to 11%. A possibility to apply the proposed method for parabens determination in water samples was demonstrated.
Rocznik
Strony
589--601
Opis fizyczny
Bibliogr. 31 poz., rys., tab.
Twórcy
autor
  • Vilnius University Department of Analytical and Environmental Chemistry Naugarduko 24 LT-03225 Vilnius Lithuania
autor
  • Vilnius University Department of Analytical and Environmental Chemistry Naugarduko 24 LT-03225 Vilnius Lithuania
autor
  • Vilnius University Department of Analytical and Environmental Chemistry Naugarduko 24 LT-03225 Vilnius Lithuania
  • Vilnius University Department of Analytical and Environmental Chemistry Naugarduko 24 LT-03225 Vilnius Lithuania
Bibliografia
  • [1] J.K. Lokhnauth and N.H. Snow, Anal. Chem., 77, 5938 (2005)
  • [2] G. Shanmugam, B.R. Ramaswamy, V. Radhakrishnan, and H. Tao, Microchem. J., 96, 391 (2010)
  • [3] P. Canosa, I. Rodriguez, E. Rubi, N. Negreira, and R. Cela, Anal. Chim. Acta, 575, 106 (2006)
  • [4] T. Benijts, W. Lambert, and A. De Leenheer, Anal. Chem., 76, 704 (2004)
  • [5] I. Gonzalez-Marino, J.B. Quintana, I. Rodriguez, S. Schrader, and M. Moeder, Anal. Chim. Acta, 684, 59 (2011)
  • [6] A.M. Casas Ferreira, M. Moder, and M.E. Fernandez Laespada, Anal. Bioanal. Chem., 399, 945 (2011)
  • [7] E. Villaverde-de-Saa, I. Gonzalez-Marino, J.B. Quintana, R. Rodil, I. Rodriguez, and R. Cela, Anal. Bioanal. Chem., 397, 2559 (2010)
  • [8] J. Regueiro, M. Llompart, E. Psillakis, J.C. Garcia-Monteagudo, and C. Garcia-Jares, Talanta, 79, 1387 (2009)
  • [9] J. Regueiro, E. Becerril, C. Garcia-Jares, and M. Llompart, J. Chromatogr. A, 1216, 4693 (2009)
  • [10] T. Benijts, W. Lambert, and A. De Leenheer, Anal. Chem., 76, 704 (2004)
  • [11] A. Prichodko, V. Sakociute, and V. Vickackaite, Chemija, 21, 112 (2010)
  • [12] M. Saraji and S. Mirmahdieh, J. Sep. Sci., 32, 988 (2009)
  • [13] S. Tayama, Y. Nakagawa, and K. Tayama, Mutat. Res., 649, 114 (2008)
  • [14] P.D. Darbre, A. Aljarrah, W.R. Miller, N.G. Coldham, M.J. Sauer, and G.S. Pope, J. Appl. Toxicol., 24, 5 (2004)
  • [15] P.D. Darbre and P.W. Harvey, J. Appl. Toxicol., 28, 561 (2008)
  • [16] J.J. Strouse, T.R. Fears, M.A. Tucker, and A.S. Wayne, J. Clin. Oncol., 23, 4735 (2005)
  • [17] M. Terasaki and M. Makino, Int. J. Environ. Anal. Chem., 88, 911 (2008)
  • [18] A.M. Peek, Anal. Bioanal. Chem., 386, 907 (2006)
  • [19] T. Okumura and Y. Nishikawa, Anal. Chim. Acta, 325, 175 (1996)
  • [20] P. Canosa, I. Rodriguez, E. Rubi, M.H. Bollain, and R. Cela, J. Chromatogr. A, 1124, 3 (2006)
  • [21] P. Canosa, I. Rodriguez, E. Rubi, and R. Cela, J. Chromatogr. A, 1072, 107 (2005)
  • [22] V. Ciuvasovaite, E. Adomaviciute, and V. Vickackaite, Chemija, 18, 11 (2007)
  • [23] Y.C. Fiamegos and C.D. Stalikas, Anal. Chim. Acta, 597, 32 (2007)
  • [24] A. Prichodko, K. Jonusaite, and V. Vickackaite, Centr. Eur. J. Chem., 7, 285 (2009)
  • [25] M.A. Farajzadeh, Gj. Djozan, and R. Fazeli Bakhtiyari, Talanta, 81, 1360 (2010)
  • [26] M. Rezaee, Y. Assadi, M.R. Milani Hosseini, E. Aghaee, F. Ahmadi, and S. Berijani, J. Chromatogr. A, 1116, 1 (2006)
  • [27] C. Basheer, H.K. Lee, and J.P. Obbard, J. Chromatogr. A, 968, 191 (2002)
  • [28] Y. Lu, Q. Lin, G. Luo, and Y. Dai, Anal. Chim. Acta, 566, 259 (2006)
  • [29] M.R.K. Zanjani, Y. Yamini, S. Shariati, and J.A. Jonsson, Anal. Chim. Acta, 585, 286 (2007)
  • [30] H. Farahani, M.R. Ganjali, R. Dinarvand, and P. Norouzi, Talanta, 76, 718 (2008)
  • [31] H.R. Sobhi, Y. Yamini, A. Esrafili, and R.H.H.B. Abadi, J. Chromatogr. A, 1196–1197, 28 (2008)
Typ dokumentu
Bibliografia
Identyfikator YADDA
bwmeta1.element.baztech-b9a2c9a4-84aa-4b9d-b222-5af2fa48ccbc
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