Evaluation and application of static headspace-multicapillary column-gas chromatography-ion mobility spectrometry for complex sample analysis

被引:48
作者
Denawaka, Chamila J. [1 ]
Fowlis, Ian A. [1 ]
Dean, John R. [1 ]
机构
[1] Northumbria Univ, Dept Appl Sci, Newcastle Upon Tyne NE1 8ST, Tyne & Wear, England
关键词
Static headspace; Multicapillary column-gas chromatography; Ion mobility spectrometry; Theory; Quantification; Foot malodour; VOLATILE ORGANIC-COMPOUNDS; CHEMICAL WARFARE AGENTS; MASS-SPECTROMETRY; MALODOR GENERATION; WATER CLUSTERS; LAUNDRY; IDENTIFICATION; ODOR; METABOLITES; EXPLOSIVES;
D O I
10.1016/j.chroma.2014.02.047
中图分类号
Q5 [生物化学];
学科分类号
070307 [化学生物学];
摘要
An evaluation of static headspace-multicapillary column-gas chromatography-ion mobility spectrometry (SHS-MCC-GC-IMS) has been undertaken to assess its applicability for the determination of 32 volatile compounds (VCs). The key experimental variables of sample incubation time and temperature have been evaluated alongside the MCC-GC variables of column polarity, syringe temperature, injection temperature, injection volume, column temperature and carrier gas flow rate coupled with the IMS variables of temperature and drift gas flow rate. This evaluation resulted in six sets of experimental variables being required to separate the 32 VCs. The optimum experimental variables for SHS-MCC-GC-IMS, the retention time and drift time operating parameters were determined; to normalise the operating parameters, the relative drift time and normalised reduced ion mobility for each VC were determined. In addition, a full theoretical explanation is provided on the formation of the monomer, dimer and trimer of a VC. The optimum operating condition for each VC calibration data was obtained alongside limit of detection (LOD) and limit of quantitation (LOQ) values. Typical detection limits ranged from 0.1 ng bis(methylthio)methane, ethylbutanoate and (E)-2-nonenal to 472 ng isovaleric acid with correlation coefficient (R-2) data ranging from 0.9793 (for the dimer of octanal) through to 0.9990 (for isobutyric acid). Finally, the developed protocols were applied to the analysis of malodour in sock samples. Initial work involved spiking an inert matrix and sock samples with appropriate concentrations of eight VCs. The average recovery from the inert matrix was 101 +/- 18% (n = 8), while recoveries from the sock samples were lower, that is, 54 +/- 30% (n = 8) for sock type 1 and 78 +/- 24% (n = 6) for sock type 2. Finally, SHS-MCC-GC-IMS was applied to sock malodour in a field trial based on 11 volunteers (mixed gender) over a 3-week period. By applying the SHS-MCC-GC-IMS database, four VCs were identified and quantified: ammonia, dimethyl disulphide, dimethyl trisulphide and butyric acid. A link was identified between the presence of high ammonia and dimethyl disulphide concentrations and a high malodour odour grading, that is, >= 6. Statistical analysis did not find any correlation between the occurrence of dimethyl disulphide and participant gender. (C) 2014 The Authors. Published by Elsevier B.V. This is an open access article under the CC BY license (http://creativecommons.org/licens es/by/3.0/).
引用
收藏
页码:136 / 148
页数:13
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