Determination of Ametryn in River Water, River Sediment and Bivalve Mussels by Liquid Chromatography-Tandem Mass Spectrometry

被引:18
作者
Jacomini, Analu E. [2 ]
de Camargo, Plinio B. [3 ]
Avelar, Wagner E. P. [2 ]
Bonato, Pierina S. [1 ]
机构
[1] Univ Sao Paulo, Dept Quim & Fis, Fac Ciencias Farmaceut Ribeirao Preto, BR-14040903 Ribeirao Preto, SP, Brazil
[2] Univ Sao Paulo, Dept Biol, Fac Filosofia Ciencias & Letras Ribeirao Preto, BR-14040901 Ribeirao Preto, SP, Brazil
[3] Univ Sao Paulo, Ctr Energia Nucl Aplicada, BR-13416000 Piracicaba, SP, Brazil
基金
巴西圣保罗研究基金会;
关键词
ametryn; liquid chromatography; mass spectrometry; method validation; environmental analysis; SOLID-PHASE EXTRACTION; ANODONTITES-TRAPESIALIS; TRIAZINE HERBICIDES; PESTICIDES; SAMPLES; BRAZIL; METABOLITES; PHENYLUREA; RESIDUES; MS/MS;
D O I
10.1590/S0103-50532009000100018
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Analytical methods employing liquid chromatography-mass spectrometry (LC-MS-MS) for ametryn determination in river water, river sediment and in freshwater bivalve mussel Corbicula fluminea are described. Liquid-liquid extraction was used for sample preparation. The analyses of ametryn in samples were performed on a reversed-phase RP-18 column with MS detection in positive electrospray and multi reaction monitoring modes. The quantitation limit of ametryn was 20 ng L-1, 0.1 ng g(-1) and 0.5 ng g(-1), for water, sediment and bivalve samples, respectively. Linearity, precision, accuracy and recovery were also reported. The results obtained for method validation are within the international limits and in accordance with literature, suggesting that the developed methods are suitable for the quantitation of ametryn in river water, river sediment and in bivalve Corbicula fluminea. These methods were applied for the analysis of samples from Mogi-Guacu River and Pardo River, Sao Paulo State. Results indicated that the highest level of ametryn was 1.44 ng g(-1) in bivalve samples from Mogi-Guacu River.
引用
收藏
页码:107 / 116
页数:10
相关论文
共 29 条
  • [1] ARMAS ED, 2005, QUIM NOVA, V28, P975, DOI DOI 10.1590/S0100-40422005000600008
  • [2] Avelar W E, 1991, An Acad Bras Cienc, V63, P337
  • [3] AVELAR WEP, 1998, CI CULT, V50, P452
  • [4] LC-ESI-MS/MS determination of phenylurea and triazine herbicides and their dealkylated degradation products in oysters
    Bichon, E.
    Dupuis, M.
    Le Bizec, B.
    Andre, F.
    [J]. JOURNAL OF CHROMATOGRAPHY B-ANALYTICAL TECHNOLOGIES IN THE BIOMEDICAL AND LIFE SCIENCES, 2006, 838 (02): : 96 - 106
  • [5] Development of a multiresidue method for analyzing herbicide and fungicide residues in bovine milk based on solid-phase extraction and liquid chromatography-tandem mass spectrometry
    Bogialli, S
    Curini, R
    Di Corcia, A
    Laganà, A
    Stabile, A
    Sturchio, E
    [J]. JOURNAL OF CHROMATOGRAPHY A, 2006, 1102 (1-2) : 1 - 10
  • [6] Validation of liquid chromatographic and gas chromatographic methods - Applications to pharmacokinetics
    Bressolle, F
    BrometPetit, M
    Audran, M
    [J]. JOURNAL OF CHROMATOGRAPHY B-BIOMEDICAL APPLICATIONS, 1996, 686 (01): : 3 - 10
  • [7] Briggs S.A., 1992, Basic guide to pesticides: their characteristics and hazards
  • [8] Herbicide leaching on a recharge area of the Guarany aquifer in Brazil
    Cerdeira, AL
    dos Santos, NAG
    Pessoa, MCPY
    Gomes, MAF
    Lanchote, VL
    [J]. JOURNAL OF ENVIRONMENTAL SCIENCE AND HEALTH PART B-PESTICIDES FOOD CONTAMINANTS AND AGRICULTURAL WASTES, 2005, 40 (01) : 159 - 165
  • [9] Sorption-desorption behavior of triazine and phenylurea herbicides in Kishon river sediments
    Chefetz, B
    Bilkis, YI
    Polubesova, T
    [J]. WATER RESEARCH, 2004, 38 (20) : 4383 - 4394
  • [10] Solid-phase extraction followed by high-performance liquid chromatography-ionspray interface-mass spectrometry for monitoring of herbicides in environmental water
    Curini, R
    Gentili, A
    Marchese, S
    Marino, A
    Perret, D
    [J]. JOURNAL OF CHROMATOGRAPHY A, 2000, 874 (02) : 187 - 198