It is possible to distinguish precious vanillin from Vanilla species (planifolia or tahitensis) from much less expensive synthetic and nature-identical vanillin on the basis of the stable isotope ratios of H and C ( 2 H/ 1 H, 13 C/ 12 C). Analysis is usually performed using GC-IRMS (Gas Chromatography - Isotope Ratio Mass Spectrometry) after solvent extraction of vanillin from the sample. Recently, head-space solid-phase microextraction (HS-SPME) has been proposed as an alternative for determining 13 C/ 12 C. The aim of this study was to develop a method to analyse 2 H/ 1 H in vanillin using SPME-GC-IRMS for the first time, by testing different operating conditions and comparing the results with those obtained after solvent extraction. The ultimate scope was to develop a quick, robust and effective method to measure 2 H/ 1 H and 13 C/ 12 C in vanillin to assess the authenticity of labelling. Almost 50 authentic samples from vanilla pods, nature-identical (ex) and synthetic vanillin and 4 commercial food products were taken into account. All the samples were subjected to HS-SPME-GC-IRMS analysis and most of them to GC-IRMS analysis after solvent extraction of vanillin. The SPME method developed for 2 H/ 1 H analysis guarantees the absence of isotopic fractionation, repeatability and reproducibility standard deviation of below 7‰ and savings in terms of time (from 30 to 5 min) and solvent. HS-SPME GC-IRMS analysis of δ 2 H and δ 13 C can be proposed as a rapid and robust method to discriminate different types of vanillin and assess the authenticity of natural vanillin, also contained in food matrices

C and H stable isotope ratio analysis using solid-phase microextraction and gas chromatography-isotope ratio mass spectrometry for vanillin authentication / Perini, Matteo; Pianezze, Silvia; Strojnik, Lidija; Camin, Federica. - In: JOURNAL OF CHROMATOGRAPHY A. - ISSN 0021-9673. - 1595:(2019), pp. 168-173. [10.1016/j.chroma.2019.02.032]

C and H stable isotope ratio analysis using solid-phase microextraction and gas chromatography-isotope ratio mass spectrometry for vanillin authentication

Camin, Federica
2019-01-01

Abstract

It is possible to distinguish precious vanillin from Vanilla species (planifolia or tahitensis) from much less expensive synthetic and nature-identical vanillin on the basis of the stable isotope ratios of H and C ( 2 H/ 1 H, 13 C/ 12 C). Analysis is usually performed using GC-IRMS (Gas Chromatography - Isotope Ratio Mass Spectrometry) after solvent extraction of vanillin from the sample. Recently, head-space solid-phase microextraction (HS-SPME) has been proposed as an alternative for determining 13 C/ 12 C. The aim of this study was to develop a method to analyse 2 H/ 1 H in vanillin using SPME-GC-IRMS for the first time, by testing different operating conditions and comparing the results with those obtained after solvent extraction. The ultimate scope was to develop a quick, robust and effective method to measure 2 H/ 1 H and 13 C/ 12 C in vanillin to assess the authenticity of labelling. Almost 50 authentic samples from vanilla pods, nature-identical (ex) and synthetic vanillin and 4 commercial food products were taken into account. All the samples were subjected to HS-SPME-GC-IRMS analysis and most of them to GC-IRMS analysis after solvent extraction of vanillin. The SPME method developed for 2 H/ 1 H analysis guarantees the absence of isotopic fractionation, repeatability and reproducibility standard deviation of below 7‰ and savings in terms of time (from 30 to 5 min) and solvent. HS-SPME GC-IRMS analysis of δ 2 H and δ 13 C can be proposed as a rapid and robust method to discriminate different types of vanillin and assess the authenticity of natural vanillin, also contained in food matrices
2019
Perini, Matteo; Pianezze, Silvia; Strojnik, Lidija; Camin, Federica
C and H stable isotope ratio analysis using solid-phase microextraction and gas chromatography-isotope ratio mass spectrometry for vanillin authentication / Perini, Matteo; Pianezze, Silvia; Strojnik, Lidija; Camin, Federica. - In: JOURNAL OF CHROMATOGRAPHY A. - ISSN 0021-9673. - 1595:(2019), pp. 168-173. [10.1016/j.chroma.2019.02.032]
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/11572/265983
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