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Validation of HPLC Method for Quantitative Determination of Pirimiphos methyl

Treść / Zawartość
Identyfikatory
Warianty tytułu
Języki publikacji
EN
Abstrakty
EN
The objective of this research to optimise the HPLC method was developed for quantitative determination of Pirimiphos-methyl. Chromatographic separation was achieved on a 250 x 4.6 mm i.d. reversed phase column Qualisil BDS 5u C18, Using deionized acetonitrile:water in the ratio of 85:15 v/v respectively as mobile phase. The eluent was monitored at 254 nm. A sharp peak was obtained for the Pirimiphos-methyl at 9.29 min. The UV Spectrophotometric method performed at 254 nm after full scan analysis using methanol as a solvent. The result revealed that both methods are suitable to carry out routine analysis of Pirimiphos methyl, However HPLC results showed high precise, accurate and sensitive than the UV Spectrophotometer. Hence HPLC method is suitable for trace analysis of Pirimiphos methyl in environmental samples.
Rocznik
Tom
Strony
93--102
Opis fizyczny
Bibliogr. 16 poz., rys., tab.
Twórcy
  • Bioscience Research Foundation, Porur, Chennai 600 116, Tamil Nadu, India
autor
  • Bioscience Research Foundation, Porur, Chennai 600 116, Tamil Nadu, India
autor
  • Bioscience Research Foundation, Porur, Chennai 600 116, Tamil Nadu, India
  • Bioscience Research Foundation, Porur, Chennai 600 116, Tamil Nadu, India
Bibliografia
  • [1] IE. Mills, Pirimiphos-methyl: blood concentrations and tissue retention in rat. Report No CTL/P/247. Imperial Chemical industries, Central toxicology laboratory, (1976)11.
  • [2] C. Cox, Journal of Pesticide Reform 2 (1996) 2.
  • [3] C. Sobarzo, E. Bustoos-Obregón, Asian Journal of Andrology 2 (2000) 147.
  • [4] E.ustos-Obregón, P. Gonzállez-Hormanzábal, Int. J. Morphol. 2 (2003) 155.
  • [5] A. E. Ghaly, F. Alkoaik, A. Snow, Canadian Biosystems Engineering 49 (2007) 61.
  • [6] Hendig Winarno, Agustin N. M. Bagyo, Winarti A. Lindu, Ermin K. Winarno, Atom Indonesia 30(2) (2004) 35.
  • [7] US Food and Drug Administration, Pesticide Analytical Manual, Vol. I, FDA, Rockville, MD, 1979.
  • [8] P. Lopez-Roldan, M. J. Lopez de Alda, D. Barcelo, Anal. Bioanal. Chem. 378 (2004) 599.
  • [9] A. Pasha, Y. N. Vijayashankar, N. G. K. Karanth, J. AOAC Int. 79 (1996) 1009.
  • [10] A. Di Corcia, M. Marchetti, Anal. Chem. 63 (1991) 580.
  • [11] O. A. Zalat, M. A. Elsayed, M. S. Fayed, M. K. Abd El Megid, International Letters of Chemistry, Physics and Astronomy 2 (2014) 58-63.
  • [12] S. Magdic, A. Boyd-Boland, K. Jinno, J. B. Pawliszyn, J. Chromatogr. A 736 (1996) 219.
  • [13] P. L. Wylie, K. Uchiyama, J. AOAC Int. 79 (1996) 571.
  • [14] B. F. Scott, J. Struger, H. Tse, J. Environ. Anal. Chem. 61 (1995) 129.
  • [15] N. K. Wilson, J. C. Chuang, C. Lyu, J. Expo. Anal. Environ. Epidemiol. 11 (2001) 449.
  • [16] D. E. Glotfelty, M. S. Majewski, J. N. Seiber, Environ. Sci. Technol. 24 (1990) 353.
Typ dokumentu
Bibliografia
Identyfikator YADDA
bwmeta1.element.baztech-2f19eae4-46f0-47dd-8777-e6ba8c1ca382
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