Subsequent Solid-phase Extraction Research Articles

Analysis of heterocyclic aromatic amines by high resolution gas chromatography-mass spectrometry: a suitable technique for the routine control of food and process flavours

Ten heterocyclic aromatic amines (HAA; [2-amino-3-methyl-3H-imidazo[4,5-f]quinoline (1); 2-amino-3,4-dimethyl-3H-imidazo[4,5-f]quinoline (2); 2-amino-3-methyl-3H-imidazo[4,5-f]quinoline (3); 2-amino-3,8-dimethyl-3H-imidazo[4,5-f]quinoline (4); 2-amino-3,4,8-trimethyl-3H-imidazo[4,5-f]quinoline (5); 2-amino-3,7,8-trimethyl-3H-imidazo[4,5-f]quinoline (6); 2amino-3,4,7,8-tetramethyl-3H-imidazo[4,5-f]quinoline (7); 2-amino-1-methyl-6-phenyl-imidazo[4,5-f]quinoline (8); 2-amino-6-methyldipyrido[1,2-α : 3′,2′-d]imidazole (9); 2-aminodipyrido[1,2-α : 3′,2′-d]imidazole (10)]) were analysed in commercially available meat products and process flavours. After sample preparation by Extrelut treatment, subsequent solid phase extraction applying propylsulphonic and C18 silica cartridges, as well as derivatization with 3,5-bis-trifluoromethylbenzyl bromide, HRGC-electron-impact-ionization-MS (HRGC-EIMS) analysis in the selected ion monitoring mode was performed. Isotope dilution analysis with 2amino-8-methyl-3-(trideuteromethyl)-3H-imidazo[4,5- f]quinoxaline and 2-amino-1-(trideuteromethyl)-6-phenyl-imidazo[4,5-b]pyridine was used to quantify 4 and 8; for 1–3, 5–7, 9 and 10, standard addition was employed as the determination method. The detection limit of 1 ng/g evaluated for 3–6 and 9 was sufficient for routine analysis, i.e. to obtain an initial insight into the grade of a potential HAA contamination of food or process flavours. To obtain more detailed information, the previously developed, more sensitive technique of HPLC-electrospray-tandem-MS (HPLC-ESI-MS/MS) has to be used, as shown by the comparison of the data obtained by HRGC-MS and HPLC-ESI-MS/MS analyses.

Determination of heterocyclic aromatic amines (HAA) in commercially available meat products and fish by high performance liquid chromatography—Electrospray tandem mass spectrometry (HPLC-ESI-MS-MS)

Ten heterocyclic aromatic amines (HAA) (1)–(10) were analyzed in commercially available meat products and fish. After sample preparation by Extrelut treatment and subsequent solid phase extraction applying propylsulphonic and C18 silica cartridges, HPLC-ESI-MS-MS using selected reaction monitoring (SRM) and d3-PhIP and d3-MeIQx as internal and external standards, respectively, revealed the widely distributed presence of PhIP (8) and MeIQx (4), ranging from 0.1 to 5.3 ng g−1 and 0.1 to 5.2 ng g−1, respectively. Lower amounts were found for 4,8-DiMeIQx (5) and 7,8-DiMeIQx (6), ranging from 0.2 to 2.0 ng g−1 and 0.1 to 0.2 ng g−1, respectively. The other HAA under study, i.e. IQ, MeIQ, 4,7,8-TriMeIQx, Glu-P-1, and Glu-P-2 were not determinable under the experimental conditions used (determination limit 0.1 ng g−1).

New strategies for trace analyses of ZrO 2 , SiC and Al 2 O 3 ceramic powders

The progress possible in the analysis of refractory powders such as ZrO2, SiC and Al2O3 by the use of new sample preparation, processing and introduction techniques elaborated for AAS, ICP-OES and ICP-MS with low and high mass resolution is demonstrated. For optimized sample preparation techniques based on dissolution of ZrO2, e.g. fusion with (NH4)2SO4, it is shown to what extent impurities present in (NH4)2SO4 determine the detection limit. Hydraulic high pressure nebulization with and without matrix removal by complexing the impurities with dithiocarbamates (Cu, Co, Cr and Ni) or oxine (Fe, Mn and Mo) and fixing them on a C18 solid phase for subsequent solid phase extraction coupled with flame atomic absorption was used to determine Fe, Cu, Cr, Mn, Ni, Co and Mo impurities in (NH4)2SO4 in the 10–100 ng/g range. Further a method to synthesize (NH4)2SO4 with higher purity than some commercially available high-purity (NH4)2SO4 with respect to Fe, Cu, Cr and Mn using high-purity NH3 and chlorosulphonic acid is shown. Reliable determinations of Fe and Al at the 100 μg/g level in ZrO2 with ICP-OES with matrix removal as well as with ICP-MS without matrix removal are reported. For the direct analysis of Al2O3 powders, slurry nebulization ICP-MS sample introduction is shown to improve detection limits and to reduce sample preparation, if the leachable and non-leachable fractions are analyzed separately. For powders such as SiC, the matrix or solvents can cause spectral interferences. Matrix removal is shown to be useful to improve detection limits for the interfered elements. High resolution ICP-MS can be used to control the completeness of matrix removal techniques and to overcome limitations due to spectral interferences even in case of complex materials.

Determination of radiation-induced hydrocarbons in processed food and complex lipid matrices

Detection of irradiated components in processed food with complex lipid matrices can be affected by two problems. First, the processed food may contain only a small amount of the irradiated component, and the radiation-induced hydrocarbons may be diluted throughout the lipid matrix of the whole food. Second, in complex lipid matrices, the detection of prior irradiation is often disturbed by fat-associated compounds. In these cases, common solid phase extraction (SPE) Florisil clean-up alone is inadequate in the detection of prior irradiation. Subsequent SPE argentation chromatography of the Florisil eluate allows the measurement of small amounts of irradiated lipid-containing ingredients in processed food as well as the detection of prior irradiation in complex lipid matrices such as paprika and chilli. SPE argentation chromatography is the first method available for the selective enrichment of radiation-specific hydrocarbons from even complex lipid matrices, thus enabling the detection of irradiation doses as low as 0.025 kGy. Furthermore, by using radiation-induced hydrocarbons in the detection of prior irradiation of paprika and chilli powder, a second independent method, the first being measurement of thermoluminescence, is available for the analysis of these matrices. Such analysis could be achieved by using this highly sensitive, cheap and easy to perform combined SPE Florisil/argentation chromatography method, without the need for sophisticated techniques like SFE-GC/MS or LC-GC/MS, so that highly sensitive detection of prior irradiation could be performed in almost every laboratory.

Analysis of ifosforamide mustard, the active metabolite of ifosfamide, in plasma.

Ifosforamide mustard is the active metabolite of ifosfamide, a cytostatic drug. In this study a sensitive and selective method for the analysis of ifosforamide mustard in plasma is described. The method consists of direct derivatisation of ifosforamide mustard in plasma with diethyldithiocarbamate and subsequent solid-phase extraction of the resulting derivative. The analysis of the derivatisation product was performed by high-performance liquid chromatography with UV detection. The calibration graph was linear in the concentration range 0.45-45 microM and the minimum detectable concentration was 0.45 mumol. The samples were stabilised by addition of semicarbazide and sodium chloride. A patient's plasma sample was analysed by means of the described method. The ifosforamide mustard concentration was 2.3 microM.

Determination of proguanil and metabolites in small sample volumes of whole blood stored on filter paper by high-performance liquid chromatography

A method is reported for the determination of proguanil and its two metabolites cycloguanil and 4-chlorophenylbiguanide in whole blood and plasma samples obtained by thumbprick and stored dry on filter paper. The sample preparation involves liquid extraction from the filter paper and subsequent solid-phase extraction using C 8 Bond-Elut cartridges. Separation and quantification is by a previously reported ion-pairing high-performance liquid chromatographic system with ODS Hypersil as stationary phase and an 50:50 acetonitrile-pH 2 phosphate buffer mobile phase containing 200 m M sodium dodecylsulphate as ion-pairing agent. The analytical characteristics of the method are reported. Representative concentrations are shown as a function of time from a human subject after ingestion of a single 200-mg dose of proguanil hydrochloride. Typical ranges of concentration detected by the proposed method in human subjects were proguanil 12–900 ng/ml, cycloguanil 16–44 ng/ml and 4-chlorophenylbiguanide 1.5–10 ng/ml in whole blood.

TRACE ANALYSIS OF PROTEIN AMINO ACIDS AS N(O, S)-ISOBUTYLOXYCARBONYL TERT.-BUTYLDIMETHYLSILYL DERIVATIVES IN AQUEOUS SAMPLES

N(O, S)-isoButyloxycarbonyl(-isoEOC) derivatization with subsequent solid-phase extraction and silylation was investigated for the trace analysis of protein amino acids in complex aqueous samples. The amino acids in basic aqueous medium were allowed to react with isobutyl chloroformate. After acidification the resulting N(O, S)-isoBOC amino acids were solid-phase extracted using Chromosorb P as solid sorbent and then converted to tert.-butyldimethylsilyl derivatives, followed by direct gas chromatographic analysis. The application of the method to the amino acid profiling of various complex samples is demonstrated.

Analysis of blood and urine samples from Macaca mulata for pyronaridine by high-performance liquid chromatography with electrochemical detection

We describe a high-performance liquid chromatographic method with electrochemical detection for quantifying pyronaridine in rhesus monkey (Macaca mulata) blood and urine samples. The detection limit is 20 ng/ml at a signal-to-noise ratio of 4 in 0.5-ml samples of blood or urine. Blood analysis includes a liquid-liquid extraction and a subsequent solid-phase extraction that removes an interferent present in blood. For urine, a back-extraction is substituted for the solid-phase extraction step. The method uses an analogue of amodiaquine as internal standard, a 10-microns rigid macroporous styrene-divinylbenzene copolymer column and a mobile phase of 1% (v/v) triethylamine in methanol-water (34:66, v/v). The method was applied to samples of blood and urine from a monkey after a single intramuscular dose of pyronaridine tetraphosphate (160 mg as base).