Determination of isopropylthioxanthone (ITX) in milk, yoghurt and fat by HPTLC-FLD, HPTLC-ESI/MS and HPTLC-DART/MS

被引:125
作者
Morlock, Gertrud [1 ]
Schwack, Wolfgang [1 ]
机构
[1] Univ Hohenheim, Inst Food Chem, D-70599 Stuttgart, Germany
关键词
planar chromatography; isopropyl-9H-thioxanthen-9-one (ITX); 2,4-diethyl-9H-thioxanthen-9-one (DTX); HPTLC-ESI/MS; HPTLC-DART/MS;
D O I
10.1007/s00216-006-0430-5
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Two new HPTLC methods for quantification of isopropyl-9H-thioxanthen-9-one (ITX) in milk, yoghurt and fat samples have been developed. Extraction of ITX from milk and yoghurt was performed with a mixture of cyclohexane and ethyl acetate by employment of accelerated solvent extraction (ASE). For soy bean oil and margarine, a simple partitioning of ITX into acetonitrile was used. ITX and 2,4-diethyl-9H-thioxanthen-9-one (DTX) used as internal standard have been separated on silica gel 60 HPTLC plates with a mixture of toluene and n-hexane (4:1, v/v) and on RP18 HPTLC plates with a mixture of acetonitrile and water (9:1, v/v). Development was performed anti-parallel from both plate sides leading to a throughput of 36 separations in 7 min. Fluorescence measurement at 254/> 400 nm was used for quantification. Limits of detection (S/N of 3) have been established to be 64 pg for ITX and DTX on both types of HPTLC plates. In fatty matrix (spiked butter) LOD of ITX was determined to be 1 mu g kg(-1). In the working range monitored (20-200 mu g kg(-1)) polynomial regression of ITX showed a relative standard deviation (sdv) of +/- 1.51 % (r=0.99981). Starting with the limit of quantification the response was linear (sdv=+/- 2.18 %, r=0.99893). Regarding repeatability (n=9) a coefficient of variation (CV) of 1.1 % was obtained for ITX at 32 ng on silica gel plates and of 2.9 % on reversed-phase plates. Repeatabilities (n=4) of ITX determination at 20, 50 and 100 mu g kg(-1) in milk, yoghurt, soybean oil and margarine showed CVs between +/- 1.0 and 6.4 %. The results prove that modern planar chromatography is a rapid and cost-efficient alternative method to quantify ITX in milk-based or fatty matrices. Only positive results are confirmed by online ESI/MS in the SIM mode (LOQ 128 pg) and by DART/MS involving a minimal employment of the MS device, which is a further advantage of HPTLC. Overall mean recovery rates of ITX at 20 or 50 and 100 mu g kg(-1) (n=8) were 41 % for milk, 70 % for yoghurt, 6 % for margarine and 12 % for soy bean oil. However, with the internal standard correction recoveries were about 130 % for milk and yoghurt and 70 and 97 % for margarine and soy bean oil, respectively.
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页码:586 / 595
页数:10
相关论文
共 11 条
[1]  
Cavalli S, 2003, LC GC EUR, P9
[2]  
Cavalli S, 2003, LC GC N AM, P35
[3]   Versatile new ion source for the analysis of materials in open air under ambient conditions [J].
Cody, RB ;
Laramée, JA ;
Durst, HD .
ANALYTICAL CHEMISTRY, 2005, 77 (08) :2297-2302
[4]  
*EUR FOOD SAF AUTH, 2005, EFSA PROV ADV SAF IT
[5]  
EURACHEM, 1998, FITN PURP AN METH
[6]  
FRANCIS ES, 2004, 227 ACS NAT M AN CA
[7]  
JAUTZ U, 2006, UNPUB ANAL CHEM
[8]   A simple device for the extraction of TLC spots: direct coupling with an electrospray mass spectrometer [J].
Luftmann, H .
ANALYTICAL AND BIOANALYTICAL CHEMISTRY, 2004, 378 (04) :964-968
[9]   New HPTLC method, with systematic mobile-phase optimization, for determination of six apolar heterocyclic aromatic amines [J].
Morlock, G .
JPC-JOURNAL OF PLANAR CHROMATOGRAPHY-MODERN TLC, 2004, 17 (06) :431-434
[10]  
MORLOCK G, 2006, UNPUB