Abstract

The bark of trees contains an interesting mixture of bioactive compounds, or so-called extractives. The use of supercritical carbon dioxide (sc-CO2) eliminates both the need for organic solvents as extractants and the danger that solvent traces might compromise the purity of the extracts. Unfortunately, the complexity and natural variability of extracts’ composition render any utilization attempts rather challenging. Thus, in order to implement exploitation concepts in a meaningful way, appropriate analytical techniques for characterizing extracts must be available beforehand. In our work, we explored gas chromatography coupled to both mass spectrometry and a flame ionization detector (GC-MS/FID), in combination with ultraperformance convergence chromatography and quadrupole time-of-flight mass spectrometry (UPC2-QTof-MS), for the characterization of bark extracts from pine (Pinus sylvestris L.) in both qualitative and quantitative terms. Although the conventional GC-MS/FID approach is a robust method for overall quantification of extractives, it fails to provide ample information about native sterol esters and triglycerides. These data are provided by a new, complementary analytical technique based on supercritical carbon dioxide, as the chromatographic eluant, coupled to a high-resolution mass spectrometer. The combination of both techniques and the use of sc-CO2 as both an extraction solvent and eluant made this combined tool especially powerful. The most prominent triglycerides in the extract were identified qualitatively and quantitatively, and the dominating sterol esters were identified qualitatively, by UPC2-QTof-MS.

Highlights

  • Lignocellulosic extractives have been used for millennia and have always been important in human history

  • gas chromatography (GC)-mass spectrometry (MS)/flame ionization detector (FID) and UPC2-ESI-QTofMS, and their results were presented for the analysis of extractives obtained from pine bark

  • GC-MS/FID was shown to be a reliable method for quantification of different families of compounds, thanks to its ability to operate at a high temperature

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Summary

■ INTRODUCTION

Lignocellulosic extractives have been used for millennia and have always been important in human history. The lock mass for gas flow (N2) of automated mass correction was based on the monoisotopic mass of leucineenkephaline (Waters): positive [M + H]+ = 556.2771 Da and negative [M − H]− = 554.2615 Da. A scan time of 0.50 s, interval of 20 s, mass window of ±0.5 Da, infusion flow rate of 5.0 μL min−1, and capillary voltage of 2.20 kV (+)/2.55 kV (−) were set as LockSpray. Mzmine.sourceforge.net), which applies four stages of processing: peak detection (the noise level was set to 5.02e2 for the positive mode and 9.0e2 for the negative mode), ADAP36 chromatogram building (Automated Data Analysis Pipeline algorithm module for chromatogram deconvolution), isotope peak grouping, and peak identification (with a homemade library containing 4,700 known extractive compounds). Each detected peak was subjected to manual validation by evaluation of the MS/MS fragmentation pattern using MassLynx software (version 4.2, Waters)

■ RESULTS AND DISCUSSION
■ CONCLUSIONS
■ ACKNOWLEDGMENTS
■ REFERENCES
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