Usefulness of D-optimal designs and multicriteria optimization in laborious analytical procedures -: Application to the extraction of quinolones from eggs

被引:33
作者
García, I
Sarabia, L
Ortiz, MC
Aldama, JM
机构
[1] Univ Burgos, Dept Chem, Fac Sci, Burgos 09001, Spain
[2] Univ Burgos, Dept Math & Computat, Fac Sci, Burgos 09001, Spain
[3] Inst Ciencias Salud Anal Fis Quim, Talavera De La Reina 45600, Toledo, Spain
关键词
D-optimal design; ciprofloxacin; enrofloxacin; residue analysis; exchange algorithm; HPLC; fluorescence; European Decision 2002/657/EC;
D O I
10.1016/j.chroma.2005.05.044
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
An analytical method has been developed to extract ciprofloxacin and enrofloxacin from eggs. The aim of this work is to determine the experimental conditions of extraction providing high recoveries with small standard deviations. An experimental design based on the D-optimality criterion and replicated three times was built to evaluate the effect of five factors related to the extraction which is the most inaccurate stage of the procedure. This non-classical design is needed because there are several practical constraints: (i) the extraction procedure is time-consuming, quinolones are not stable and the design must be performed in a single working session. (ii) The tube capacity of the centrifuge is 6, so the number of experiments will be 6 or a multiple of 6. In the optimal experimental conditions, the extraction is performed once with 5 ml of methanol. Then, fatty acids are removed with a mixture of hexane/ether. Analytes are finally separated and detected by HPLC-fluorescence without the additional step of purification by solid-phase extraction (SPE). Under these conditions, the mean recovery is 64% and 70% and the standard deviation 5% and 4% for ciprofloxacin and enrofloxacin, respectively. The capability of decision, CC alpha, is 3.1 and 2.8 mu g kg(-1) of ciprofloxacin and enrofloxacin, respectively. The capability of detection, CC beta, is 7.8 and 7.0 mu g kg(-1) of ciprofloxacin and enrofloxacin, respectively. In both cases the probabilities of false positive, alpha, and of false negative, beta, were fixed at 0.05. (c) 2005 Elsevier B.V. All rights reserved.
引用
收藏
页码:190 / 198
页数:9
相关论文
共 37 条
  • [1] [Anonymous], NEMRODW VERSION 2000
  • [2] Atkinson A.C., 1992, OPTIMUM EXPT DESIGNS
  • [3] Methods of analysis olf 4-quinolone antibacterials
    Belal, F
    Al-Majed, AA
    Al-Obaid, AM
    [J]. TALANTA, 1999, 50 (04) : 765 - 786
  • [4] OPTIMIZATION IN IRREGULARLY SHAPED REGIONS - PH AND SOLVENT STRENGTH IN REVERSED-PHASE HIGH-PERFORMANCE LIQUID-CHROMATOGRAPHY SEPARATIONS
    BOURGUIGNON, B
    DEAGUIAR, PF
    KHOTS, MS
    MASSART, DL
    [J]. ANALYTICAL CHEMISTRY, 1994, 66 (06) : 893 - 904
  • [5] Carlson R., 1992, Design and Optimization in Organic Synthesis
  • [6] Analysis of fluoroquinolones in biological fluids by high-performance liquid chromatography
    Carlucci, G
    [J]. JOURNAL OF CHROMATOGRAPHY A, 1998, 812 (1-2) : 343 - 367
  • [7] Determination of enrofloxacin and its metabolite ciprofloxacin in goat milk by high-performance liquid chromatography with diode-array detection - Optimization and validation
    Cinquina, AL
    Roberti, P
    Giannetti, L
    Longo, F
    Draisci, R
    Fagiolo, A
    Brizioli, NR
    [J]. JOURNAL OF CHROMATOGRAPHY A, 2003, 987 (1-2) : 221 - 226
  • [8] D-optimal designs
    deAguiar, PF
    Bourguignon, B
    Khots, MS
    Massart, DL
    PhanThanLuu, R
    [J]. CHEMOMETRICS AND INTELLIGENT LABORATORY SYSTEMS, 1995, 30 (02) : 199 - 210
  • [9] Simultaneous determination of six quinolones in pig muscle by liquid chromatography-atmospheric pressure chemical ionisation mass spectrometry
    Delepine, B
    Hurtaud-Pessel, D
    Sanders, P
    [J]. ANALYST, 1998, 123 (12) : 2743 - 2747
  • [10] Optimization of headspace solid-phase microextraction by means of an experimental design for the determination of methyl tert.-butyl ether in water by gas chromatography-flame ionization detection
    Dron, J
    Garcia, R
    Millán, E
    [J]. JOURNAL OF CHROMATOGRAPHY A, 2002, 963 (1-2) : 259 - 264