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2006•Journal of Planar Chromatography – Modern TLCRequires access

HPTLC determination of xanthohumol in hops (Humulus lupulusL.) and hop products

Javor Kac, Aleš Mlinarič, Andrej Umek

Open publisher page 14 citations

Abstract

A sensitive thin-layer chromatographic method has been established for quantification of xanthohumol in hops ( Humulus lupulus L.) and hop products. Chromatographic separation was performed on silica gel 60 HPTLC plates with toluene-dioxane-acetic acid, 77 + 20 + 3 ( v/v ), as mobile phase. The plates were scanned densito-metrically at λ = 368 nm. The method was validated for precision, repeatability, and accuracy. It was found to be precise — intra-day and inter-day RSD were 1.7% and 2.3%, respectively. Instrumental precision and repeatability for the method were found to be 0.38 and 1.5 (% CV ), respectively. The accuracy was checked by measuring the recovery at three levels; average recovery was 103.9%. The method was used for the estimation of xanthohumol in hop extracts and xanthohumol-enriched beer and was confirmed to be suitable for this purpose.

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What this paper is about

A sensitive thin-layer chromatographic method has been established for quantification of xanthohumol in hops ( Humulus lupulus L.) and hop products. Chromatographic separation was performed on silica gel 60 HPTLC plates with toluene-dioxane-acetic acid, 77 + 20 + 3 ( v/v ), as mobile phase. The plates were scanned densito-metrically at λ = 368 nm. The method was validated for precision, repeatability, and accuracy. It was found to be precise — intra-day and inter-day RSD were 1.7% and 2.3%, respectively. Instrumental precision and repeatability for the method were found to be 0.38 and 1.5 (% CV ), respectively. The accuracy was checked by measuring the recovery at three levels; average recovery was 103.9%. The method was used for the estimation of xanthohumol in hop extracts and xanthohumol-enriched beer and was confirmed to be suitable for this purpose.

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Available abstract

A sensitive thin-layer chromatographic method has been established for quantification of xanthohumol in hops ( Humulus lupulus L.) and hop products. Chromatographic separation was performed on silica gel 60 HPTLC plates with toluene-dioxane-acetic acid, 77 + 20 + 3 ( v/v ), as mobile phase. The plates were scanned densito-metrically at λ = 368 nm. The method was validated for precision, repeatability, and accuracy. It was found to be precise — intra-day and inter-day RSD were 1.7% and 2.3%, respectively. Instrumental precision and repeatability for the method were found to be 0.38 and 1.5 (% CV ), respectively. The accuracy was checked by measuring the recovery at three levels; average recovery was 103.9%. The method was used for the estimation of xanthohumol in hop extracts and xanthohumol-enriched beer and was confirmed to be suitable for this purpose.

Key concepts: Xanthohumol, Humulus lupulus, Hop (telecommunications), Repeatability, Chromatography, Chemistry, Acetic acid, Silica gel

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