Exploiting green sorbents in rotating-disk sorptive extraction for the determination of parabens by high-performance liquid chromatography with tandem electrospray ionization triple quadrupole mass spectrometry

被引:22
作者
Vieira, Camila M. S. [1 ]
Mazurkieviczi, Melaine [1 ]
Lopez Calvo, Angela Maria [2 ]
Debatin, Vitor [1 ]
Micke, Gustavo Amadeu [1 ]
Richter, Pablo [3 ]
Rosero-Moreano, Milton [2 ]
da Rocha, Eduardo Carasek [1 ]
机构
[1] Univ Fed Santa Catarina, Dept Quim, BR-88040900 Florianopolis, SC, Brazil
[2] Univ Caldas, Fac Ciencias Exactas & Nat, Dept Quim, GICTA, Manizales, Colombia
[3] Univ Chile, Dept Quim Inorgan & Analitica, Fac Ciencias Quim & Farmaceut, Santiago, Chile
关键词
cork; montmorillonite clay; parabens; rotating; disk sorptive extraction; water; MOLECULARLY IMPRINTED POLYMER; SOLID-PHASE MICROEXTRACTION; POLYCYCLIC AROMATIC-HYDROCARBONS; PUBLIC-HEALTH SIGNIFICANCE; HUMAN BREAST-TUMORS; WATER SAMPLES; WASTE-WATER; HPLC DETERMINATION; HUMAN URINE; CORK;
D O I
10.1002/jssc.201800426
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
In this study, the viability of applying cork and montmorillonite clay modified with ionic liquid as biosorbents in the rotating-disk sorptive extraction technique was investigated. Specifically, this was aimed at the determination of methyl paraben, ethyl paraben, propyl paraben, and isobutyl paraben, with separation/determination by high-performance liquid chromatography coupled with mass spectrometry. The optimization of the method for both biosorbents was performed using multivariate procedures. The extraction efficiencies for the target compounds in aqueous matrices were compared to those obtained using the commercial sorbent Octadecil Silano-C18. The optimum extraction conditions for both natural sorbents were the use of an ammonia solution (pH 10) as desorption solvent and an extraction time of 30 min. The proposed methods show limits of quantification of 0.8 mu g/L for cork, 3.0 mu g/L for montmorillonite clay and 6.0 mu g/L for Octadecil Silano-C18. The relative recoveries from river water and tap water samples ranged from 80.3 to 118.7% and 80.0 to 119.9% for cork and montmorillonite clay modified with ionic liquid, respectively. Relative standard deviations were obtained for intra-and interday precisions of <15% and <19% for cork and <19% and <17% for montmorillonite clay modified with ionic liquid.
引用
收藏
页码:4047 / 4054
页数:8
相关论文
共 50 条
  • [21] Validation of a method for the determination of tributyltin in seawater by stir bar sorptive extraction-liquid chromatography tandem mass spectrometry
    Camino-Sanchez, F. J.
    Zafra-Gomez, A.
    Oliver-Rodriguez, B.
    Ruiz-Naranjo, I.
    Ruiz-Garcia, J.
    Vilchez, J. L.
    JOURNAL OF CHROMATOGRAPHY A, 2012, 1263 : 14 - 20
  • [22] Photodegradation of the antibiotic spiramycin studied by high-performance liquid chromatography-electrospray ionization-quadrupole time-of-flight mass spectrometry
    Voigt, Melanie
    Savelsberg, Christina
    Jaeger, Martin
    TOXICOLOGICAL AND ENVIRONMENTAL CHEMISTRY, 2017, 99 (04) : 624 - 640
  • [23] Determination of pesticide residues in wine by membrane-assisted solvent extraction and high-performance liquid chromatography-tandem mass spectrometry
    Moeder, M.
    Bauer, C.
    Popp, P.
    van Pinxteren, M.
    Reemtsma, T.
    ANALYTICAL AND BIOANALYTICAL CHEMISTRY, 2012, 403 (06) : 1731 - 1741
  • [24] Factorial Design Optimisation of Solid Phase Extraction for Preconcentration of Parabens in Wastewater Using Ultra-High Performance Liquid Chromatography Triple Quadrupole Mass Spectrometry
    Muckoya, Vallerie A.
    Nomngongo, Philiswa N.
    Ngila, Jane C.
    CURRENT ANALYTICAL CHEMISTRY, 2020, 16 (04) : 436 - 446
  • [25] Determination of parabens in domestic sewage by isotope-coded derivatization coupled with high performance liquid chromatography-tandem mass spectrometry
    Che, Dandan
    Sun, Zhiwei
    Cheng, Jie
    Dou, Kun
    Ji, Zhongyin
    Chen, Guang
    Li, Guoliang
    You, Jinmao
    MICROCHEMICAL JOURNAL, 2017, 130 : 420 - 427
  • [26] Simultaneous determination of urinary parabens, bisphenol A, triclosan, and 8-hydroxy-2′-deoxyguanosine by liquid chromatography coupled with electrospray ionization tandem mass spectrometry
    Lu Ren
    Jianzhang Fang
    Guihua Liu
    Jianqing Zhang
    Zhou Zhu
    Honghe Liu
    Kai Lin
    Huimin Zhang
    Shaoyou Lu
    Analytical and Bioanalytical Chemistry, 2016, 408 : 2621 - 2629
  • [27] Electro-oxidation of diclofenac in methanol as studied by high-performance liquid chromatography/electrospray ionization mass spectrometry
    Franski, Rafal
    Zalas, Maciej
    Gierczyk, Blazej
    Schroeder, Grzegorz
    RAPID COMMUNICATIONS IN MASS SPECTROMETRY, 2016, 30 (13) : 1662 - 1666
  • [28] C18-coated stir bar sorptive extraction combined with high performance liquid chromatography-electrospray tandem mass spectrometry for the analysis of sulfonamides in milk and milk powder
    Yu, Chunhe
    Hu, Bin
    TALANTA, 2012, 90 : 77 - 84
  • [29] Determination of ethylenediaminetetraacetic acid in nuclear waste by high-performance liquid chromatography coupled with electrospray mass spectrometry
    de Maquille, Laurence du Bois
    Renaudin, Laetitia
    Goutelard, Florence
    Jardy, Alain
    Vial, Jerome
    Thiebaut, Didier
    JOURNAL OF CHROMATOGRAPHY A, 2013, 1276 : 20 - 25
  • [30] Pesticide residue determination in surface waters by stir bar sorptive extraction and liquid chromatography/tandem mass spectrometry
    Giordano, A.
    Fernandez-Franzon, M.
    Ruiz, M. J.
    Font, G.
    Pico, Y.
    ANALYTICAL AND BIOANALYTICAL CHEMISTRY, 2009, 393 (6-7) : 1733 - 1743