Elsevier

Analytical Biochemistry

Volume 499, 15 April 2016, Pages 1-7
Analytical Biochemistry

A high-throughput method for liquid chromatography–tandem mass spectrometry determination of plasma alkylresorcinols, biomarkers of whole grain wheat and rye intake

https://doi.org/10.1016/j.ab.2015.12.023Get rights and content

Abstract

Plasma alkylresorcinols are increasingly analyzed in cohort studies to improve estimates of whole grain intake and their relationship with disease incidence. Current methods require large volumes of solvent (>10 ml/sample) and have relatively low daily sample throughput. We tested five different supported extraction methods for extracting alkylresorcinols from plasma and improved a normal-phase liquid chromatography coupled to a tandem mass spectrometer method to reduce sample analysis time. The method was validated and compared with gas chromatography–mass spectrometry analysis. Sample preparation with HybridSPE supported extraction was most effective for alkylresorcinol extraction, with recoveries of 77–82% from 100 μl of plasma. The use of 96-well plates allowed extraction of 160 samples per day. Using a 5-cm NH2 column and heptane reduced run times to 3 min. The new method had a limit of detection and limit of quantification equivalent to 1.1–1.8 nmol/L and 3.5–6.1 nmol/L plasma, respectively, for the different alkylresorcinol homologues. Accuracy was 93–105%, and intra- and inter-batch precision values were 4–18% across different plasma concentrations. This method makes it possible to quantify plasma alkylresorcinols in 100 μl of plasma at a rate of at least 160 samples per day without the need for large volumes of organic solvents.

Section snippets

Chemicals and sample preparation plates

All solvents were HPLC (high-performance liquid chromatography) or LC–MS grade from Sigma–Aldrich (Stockholm, Sweden). Alkylresorcinol standards—heptadecylresorcinol (C17:0), nonadecylresorcinol (C19:0), H42-nonadecylresorcinol (H42–C19:0), heneicosylresorcinol (C21:0), tricosylresorcinol (C23:0), and pentacosylresorcinol (C25:0)—were purchased from ReseaChem (Burgsdorf, Switzerland). The phospholipid removal plates tested were Oasis (Waters, Manchester, UK), Phree (Phenomenex, Værløse,

Plate comparison

Based on the comparison of total alkylresorcinol area, area relative to internal standard, variation of peak area for alkylresorcinols, and internal standard for three phospholipid removal plates and two SLE plates, we determined that extraction on HybridSPE plates with acetone gave the best performance for total alkylresorcinol peak area and variability. Further optimization for extraction volume and solvent additive concluded that the addition of acid to the extraction solvent did not improve

Discussion

Plasma alkylresorcinols are one of the better studied dietary intake biomarkers to date, with validation studies suggesting that they fulfill the main criteria for a dietary biomarker [18], [25], leading to increased demand for their analysis in both observational and intervention studies. However, the throughput of the currently available methods is low compared with many common clinical analyses using enzyme-linked immunosorbent assay (ELISA) methods. Efforts to find suitable antibodies for

Conclusions

This new sample preparation and normal-phase LC–MS/MS method dramatically cuts down the time required to extract and analyze plasma alkylresorcinols and uses a third of the solvent required for sample preparation for GC–MS analysis. Based on our instrumentation, we were able to analyze plasma alkylresorcinols from only 100 μl of plasma, with one experienced laboratory worker able to comfortably analyze 160 samples per day, in addition to calibration curve and quality control samples. This

Conflict of interest statement

I.B. and J-P.G. are employees of the Nestlé Research Centre, part of the Nestlé company that produces a range of food and beverage products. None of the other authors declares any conflict of interest.

Acknowledgments

This work was supported in part by a grant to A.B.R. by the Chalmers Foundation, part of the Chalmers University of Technology, Gothenburg, Sweden. We thank the sales representatives from the respective plate manufacturers for kindly donating the sample preparation plates tested in this study, Per Strömberg for providing blank plasma samples, and Annette Almgren for drawing blood samples used during testing. Anders Franzén (Bergman Labora) and Anja Grüning and Dirk Jacobi (Shimadzu Europe) are

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