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Automated High-Throughput Quantification of Phenyl-γ-valerolactones and Creatinine in Urine by Laser Diode Thermal Desorption.
Lessard-Lord, Jacob; Auger, Serge; Demers, Sarah; Plante, Pier-Luc; Picard, Pierre; Desjardins, Yves.
Affiliation
  • Lessard-Lord J; Institute of Nutrition and Functional Foods (INAF), Faculty of Agriculture and Food Sciences, Laval University, 2440 Boulevard Hochelaga, Québec, Québec G1V 0A6, Canada.
  • Auger S; Nutrition, Health and Society Centre (NUTRISS), INAF, Laval University, 2440 boulevard Hochelaga, Québec, Québec G1V 0A6, Canada.
  • Demers S; Department of Plant Science, Faculty of Agriculture and Food Sciences, Laval University, 2425 Rue de l'Agriculture, Québec, Québec G1V 0A6 Canada.
  • Plante PL; Phytronix Technologies, 4535, Boulevard Wilfrid-Hamel, Suite #120, Québec, Québec G1P 2J7, Canada.
  • Picard P; Phytronix Technologies, 4535, Boulevard Wilfrid-Hamel, Suite #120, Québec, Québec G1P 2J7, Canada.
  • Desjardins Y; Institute of Nutrition and Functional Foods (INAF), Faculty of Agriculture and Food Sciences, Laval University, 2440 Boulevard Hochelaga, Québec, Québec G1V 0A6, Canada.
J Agric Food Chem ; 71(44): 16787-16796, 2023 Nov 08.
Article in En | MEDLINE | ID: mdl-37890868
Quantification of nutritional biomarkers is crucial to accurately assess the dietary intake of different classes of (poly)phenols in large epidemiological studies. High-throughput analysis is mandatory to apply this methodology in large cohorts. However, the current validated methods to quantify (poly)phenols metabolites in biological fluids use ultra performance liquid chromatography (UPLC), leading to analysis time of several minutes per sample. To significantly reduce the run time, we developed and validated a method to quantify in urine the flavan-3-ols biomarkers, phenyl-γ-valerolactones (PVLs), using laser diode thermal desorption (LDTD). This mass spectrometry source allows direct introduction of sample extracts, resulting in analysis time of less than 10 s per sample. Also, to encompass the problem associated with the cost and availability of sulfated and glucuronide analytical standards, urine samples were subjected to enzymatic hydrolysis. Creatinine was also quantified to normalize the results obtained from the urinary spot. Results obtained with LDTD-MS/MS were cross-validated by UPLC-MS/MS using 155 urine samples. Coefficient of correlation was above 0.975 for PVLs and creatinine. For all analytes, the accuracy was between 90% and 113% by LDTD-MS/MS. Altogether, sample preparation was fully automated to demonstrate the application potential of this method to large cohorts.
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Tandem Mass Spectrometry / Lasers Language: En Journal: J Agric Food Chem Year: 2023 Document type: Article Affiliation country: Canada Country of publication: United States

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Tandem Mass Spectrometry / Lasers Language: En Journal: J Agric Food Chem Year: 2023 Document type: Article Affiliation country: Canada Country of publication: United States