Cloud Point-Dispersive Liquid–Liquid Microextraction for Extraction of Organic Acids from Biological Samples
详细信息    查看全文
  • 作者:Ali Daneshfar (1)
    Tahere Khezeli (1)
  • 关键词:Cloud point ; Dispersive liquid–liquid microextraction ; HPLC–UV
  • 刊名:Journal of Surfactants and Detergents
  • 出版年:2014
  • 出版时间:November 2014
  • 年:2014
  • 卷:17
  • 期:6
  • 页码:1259-1267
  • 全文大小:492 KB
  • 参考文献:1. Penner N, Ramanathan R, Zgoda-Pols J, Chowdhury S (2010) Quantitative determination of hippuric and benzoic acids in urine by LC-MS/MS using surrogate standards. J Pharm Biomed Anal 52:534-43 CrossRef
    2. Lu Sh (2006) Voltammetric determination of nicotinic acid by glassy-carbon electrode modified with multiwall carbon nanotubes. Russ J Electrochem 42:163-66 CrossRef
    3. Capella-Peiro ME, Carda-Broch S, Monferrer-Pons L, Esteve-Romero J (2004) Micellar liquid chromatographic determination of nicotinic acid and nicotinamide after precolumn K?nig reaction derivatization. Anal Chim Acta 517:81-7 CrossRef
    4. Zhu Y, Guan X, Ji H (2009) Electrochemical solid phase microextraction and determination of salicylic acid from blood samples by cyclic voltammetry and differential pulse voltammetry. J Solid State Electrochem 13:1417-423 CrossRef
    5. Razo-Flores E, Smulders P, Prenafeta-Boldl F, Lettinga G, Field JA (1999) Treatment of anthranilic acid in an anaerobic expanded granular sludge bed reactor at low concentrations. Water Sci Technol 40:187-94 CrossRef
    6. Lillenberg M, Yurchenko S, Kipper K, Herodes K, Pihl V, Sepp K, Lohmus R, Nei L (2009) Simultaneous determination of fluoro quinolones, sulfonamides and tetracyclines in sewage sludge by pressurized liquid extraction and liquid chromatography electrospray ionization-mass spectrometry. J Chromatogr A 1216:5949-954 CrossRef
    7. Herrera-Herrera AV, Hernandez-Borgesa J, Rodriguez-Delgado MA, Herrero M, Cifuentes A (2011) Determination of quinolone residues in infant and young children powdered milk combining solid phase extraction and ultra-performance liquid chromatography-tandem mass spectrometry. J Chromatogr A 1218:7608-614 CrossRef
    8. Moliner-Martinez Y, Vitta Y, Prima-Garcia H, Gonzalez-Fuenzalida RA, Ribera A, Campins-Falco P, Coronado E (2013) Silica supported Fe3O4 magnetic nanoparticles for magnetic solid-phase extraction and magnetic in-tube solid phase microextraction: application to organophosphorous compounds. Anal Bioanal Chem 406:2211-215 CrossRef
    9. Soini HA, Bruce KE, Wiesler D, David F, Sandra P, Novotny MV (2005) Stir bar sorptive extraction: a new quantitative and comprehensive sampling technique for determination of chemical signal profiles from biological media. J Chem Ecol 31:377-92 CrossRef
    10. Zhao RS, Yuan JP, Li HF, Wang X, Jiang T, Lin JM (2007) Nonequilibrium hollow-fiber liquid-phase microextraction with in situ derivatization for the measurement of triclosan in aqueous samples by gas chromatography-mass spectrometry. Anal Bioanal Chem 387:2911-915 CrossRef
    11. Frenich AG, Romero-Gonzalez R, Vidal JLM, Martinez OR, Baquero FP (2011) Comparison of solid phase microextraction and hollow fiber liquid phase microextraction for the determination of pesticides in aqueous samples by gas chromatography triple quadrupole tandem mass spectrometry. Anal Bioanal Chem 399:2043-059 CrossRef
    12. Tsai WC, Huang SD (2009) Dispersive liquid–liquid–liquid microextraction combined with liquid chromatography for the determination of chlorophenoxy acid herbicides in aqueous samples. J Chromatogr A 1216:7846-850 CrossRef
    13. Rezaee M, Assadi Y, Hosseini MRM, Aghaee E, Ahmadi F, Berijani S (2006) Determination of organic compounds in water using dispersive liquid–liquid microextraction. J Chromatogr A 1116:1-
文摘
A new method combining cloud point extraction (CPE) with dispersive liquid–liquid microextraction (DLLME) named “cloud point-dispersive liquid–liquid microextraction (CP-DLLME)-was presented in this work for the first time for the determination of organic acids as model compounds in biological samples using high performance liquid chromatography and UV detection (HPLC–UV). Water (disperser solvent) containing tert-octylphenol ethoxylate (7.5EO) as extraction solvent, was rapidly injected into a warmed sample solution and cloudy state formed immediately. After that, phase separation was performed by centrifugation. The surfactant-rich phase was diluted with acetonitrile and injected into a HPLC–UV apparatus. The influence of several important parameters on the extraction efficiencies was evaluated. Under optimized experimental conditions, the calibration graphs were linear in the range of 0.06-,500?μg L? for target analytes. Coefficient of determination (r 2) ranged from 0.9985 to 0.9994. The limits of detection were in the range of 0.05-7.1?μg L?. The new method was successfully applied with satisfactory results for analysis of target analytes in spiked samples. The relative mean recoveries of the spiked samples ranged from 91.8 to 107.1?% with relative standard deviations in the range of 2.1 to 4.3?%.

© 2004-2018 中国地质图书馆版权所有 京ICP备05064691号 京公网安备11010802017129号

地址:北京市海淀区学院路29号 邮编:100083

电话:办公室:(+86 10)66554848;文献借阅、咨询服务、科技查新:66554700