Essential-Oil Analysis of Irradiated Spices by Using Comprehensive Two-Dimensional Gas Chromatography

ChemPlusChem ◽  
2014 ◽  
Vol 79 (6) ◽  
pp. 798-803 ◽  
Author(s):  
Celale Kirkin ◽  
Blagoj Mitrevski ◽  
Gurbuz Gunes ◽  
Philip J. Marriott
Molecules ◽  
2010 ◽  
Vol 15 (10) ◽  
pp. 7006-7015 ◽  
Author(s):  
Syarul Nataqain Baharum ◽  
Hamidun Bunawan ◽  
Ma’aruf Abd. Ghani ◽  
Wan Aida Wan Mustapha ◽  
Normah Mohd Noor

2016 ◽  
Vol 39 (24) ◽  
pp. 4765-4772 ◽  
Author(s):  
Ján Krupčík ◽  
Roman Gorovenko ◽  
Ivan Špánik ◽  
Daniel W. Armstrong ◽  
Pat Sandra

Foods ◽  
2019 ◽  
Vol 8 (11) ◽  
pp. 580 ◽  
Author(s):  
Mariosimone Zoccali ◽  
Barbara Giocastro ◽  
Ivana L. Bonaccorsi ◽  
Alessandra Trozzi ◽  
Peter Q. Tranchida ◽  
...  

The present research is focused on the in-depth qualitative analysis of three types of lime essential oil (EO), viz., Key (A and B) and Persian, using the off-line combination of normal phase high performance liquid chromatography (NP-HPLC) and comprehensive two-dimensional gas chromatography–quadrupole mass spectrometry (GC × GC-QMS). The first analytical dimension (NP-HPLC) was exploited for the isolation of the hydrocarbon constituents from the oxygenated ones. Each fraction was then reduced in volume and analyzed using (cryogenic modulation) GC × GC-QMS. Peak assignment was carried out through the combined use of mass spectral database and linear retention index matching processes. The powerful four-dimensional technology enabled the separation and identification of a very high number (153) of lime essential oil volatile compounds.


2008 ◽  
Vol 3 (7) ◽  
pp. 1934578X0800300
Author(s):  
Peter Quinto Tranchida ◽  
Rosaria Costa ◽  
Paola Dugo ◽  
Giovanni Dugo ◽  
Luigi Mondello

The present research is focused on the use of micro-bore column fast gas chromatography in combination with rapid-scanning quadrupole mass spectrometry for mediumly-complex essential oil analysis. A basil essential oil sample was initially subjected to conventional GC-MS (analysis time: 25 min) under optimum analytical conditions. Peak identification was carried by using a dual-filtered MS library search procedure: the first filter deleted “hits” with a less than 90% spectral similarity, while the second filter eliminated matches with a linear retention index (LRI) outside a pre-defined LRI window. The same essential oil sample was analyzed under optimized fast GC-MS conditions by using a micro-bore column, with the same aforementioned MS library search process (analysis time: 5.3 min). Resolution was altogether similar in both applications, with the same number of compounds reliably-identified, namely fifty-nine. The experiment demonstrated the usefulness of the rapid GC approach in this type of experiment.


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