Chromatographic and spectroscopic characterization of urolithins for their determination in biological samples after the intake of foods containing ellagitannins and ellagic acid

•LC, UV and MS (QQQ and QTOF) characteristics of urolithin standards were studied.•Relative response factors in UV at 305nm respect to Uro-A or EA were calculated.•We provide useful data for urolithin analysis when standards are not available.•Methods were validated for their application in urine, f...

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Published inJournal of Chromatography A Vol. 1428; pp. 162 - 175
Main Authors García-Villalba, Rocío, Espín, Juan Carlos, Tomás-Barberán, Francisco A.
Format Journal Article
LanguageEnglish
Published Netherlands Elsevier B.V 08.01.2016
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Summary:•LC, UV and MS (QQQ and QTOF) characteristics of urolithin standards were studied.•Relative response factors in UV at 305nm respect to Uro-A or EA were calculated.•We provide useful data for urolithin analysis when standards are not available.•Methods were validated for their application in urine, feces and plasma samples.•Biological samples were analyzed after the intake of ellagitannin-containing foods. Ellagitannins and ellagic acid (EA) are metabolized by the gut microbiota to produce urolithins that could be responsible for the health effects attributed to ellagitannin-containing food products. Several urolithin aglycones could be present in fecal samples while glucuronide and sulphate conjugates are mainly found in plasma and urine. So far, the lack of available standards has made difficult their correct identification and quantification. In the present study, UV and MS spectra characteristics of urolithins and their phase II metabolites have been determined using different systems based on liquid chromatography (LC) coupled with diode-array or mass spectrometer detectors with different analyzers (triple quadrupole (QqQ) and quadrupole time-of-flight (QTOF)). Chromatographic separation was achieved on a reversed-phase Poroshell C18 column (3×100mm, 2.7μm). Elution order, characteristic UV spectra, and relative response factors (RRFs) with respect to their parental compound (EA) and the most common metabolite urolithin A (Uro-A) were determined. This contribution, along with the most important mass spectra characteristics (MRM transitions, qualifier/quantifier ratio, accurate mass and fragmentation pattern) will allow the determination of urolithin metabolites in different biological samples and their quantification even if not all metabolites are commercially available. The methods developed in the three systems have been fully validated in terms of linearity, sensitivity, precision, recovery, matrix effect, selectivity and stability. After that, they were successfully applied to complex biological matrices (urine, feces and plasma) from two human studies in which volunteers consumed ellagitannin-containing foods, such as walnuts and pomegranate extracts.
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ISSN:0021-9673
1873-3778
DOI:10.1016/j.chroma.2015.08.044