Two-Dimensional Retention Indices Improve Component Identification in Comprehensive Two-Dimensional Gas Chromatography of Saffron

被引:67
作者
Jiang, Ming [1 ]
Kulsing, Chadin [2 ]
Nolvachai, Yada [2 ]
Marriott, Philip J. [2 ]
机构
[1] Huazhong Univ Sci & Technol, Sch Pharm, Tongji Med Coll, Wuhan 430030, Hubei, Peoples R China
[2] Monash Univ, Australian Ctr Res Separat Sci, Sch Chem, Clayton, Vic 3800, Australia
基金
澳大利亚研究理事会; 中国国家自然科学基金;
关键词
FLIGHT MASS-SPECTROMETRY; CROCUS-SATIVUS L; VOLATILE COMPONENTS; CAROTENOIDS;
D O I
10.1021/acs.analchem.5b00953
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
Comprehensive two-dimensional gas chromatography hyphenated with accurate mass time-of-flight mass spectrometry (GC X GC-accTOFMS) Was applied for improved analytical accuracy of saffron analysis, by using retention indices in the two-dimensional separation. This constitutes 3 dimensions of identification. In addition to accTOFMS specificity, and first dimension retention indices (I-1), a simple method involving direct multiple injections with stepwise isothermal temperature programming is described for construction of isovolatility curves for reference alkane series in GC X GC. This gives access to calculated second dimension retention indices (I-2). Reliability of the calculated I-2 was evaluated by using a Grob test mixture, and saturated alkanes, revealing good correlation between previously reported I values from the literature, with R-2 correlation being,0.9997. This essentially recognizes the retention property of peaks in the GC x GC 2D space as being reducible to a retention index in each. dimension, which should be a valuable tool supporting identification. The benefit of I-2 data, in supplementing I-1 and MS library matching, was clearly demonstrated by the progressive reduction of the number of possible compound matches for peaks observed in saffron: 114 analytes were assessed according to I-1 and I-2 values within +/- 20 index unit of reference values, and by MS. spectrum matching above a match,statistic of 750 (including mass accuracy of the molecular ion <20 ppm) and their possible identities derived. The described method provides a new avenue to utilize the full capability of the two-dimensional separation (GC X GC), in combination with MS library matching in complex sample analysis, to provide improved component identification.
引用
收藏
页码:5753 / 5761
页数:9
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