首页> 外文期刊>Analytical chemistry >Analytical Condition Setting a Crucial Step in the Quantification of Unstable Polyphenols in Acidic Conditions: Analyzing Prenylflavanoids in Biological Samples by Liquid Chromatography-Electrospray Ionization Triple Quadruple Mass Spectrometry
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Analytical Condition Setting a Crucial Step in the Quantification of Unstable Polyphenols in Acidic Conditions: Analyzing Prenylflavanoids in Biological Samples by Liquid Chromatography-Electrospray Ionization Triple Quadruple Mass Spectrometry

机译:分析条件在酸性条件下的不稳定多酚定量中设置了关键步骤:通过液相色谱-电喷雾电离三重四极杆质谱法分析生物样品中的异戊二烯类黄酮

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摘要

The interest in studying hops and beer prenylflavanoids, isoxanthohumol, xanthohumol, and 8-prenylnaringenin, has increased in recent years due to their biological activity as strong phytoestrogens and potent cancer chemopreventive agents. However, prenylflavanoids behave differently from most polyphenols, since they are unstable at acidic pH. To our knowledge, no published studies to date have considered the degradation of these compounds during analytical processes. In the present work, a new sensitive and specific method based on solid phase extraction and liquid chromatography coupled to electrospray ionization triple quadruple mass spectrometry (LC-ESI-MS/MS) was developed and validated. The new method was optimized to avoid degradation of the selected analytes, isoxanthohumol, xanthohumol, and 8-prenylnaringenin, throughout the analytical process and to reduce the urine matrix effect in LC-ESI-MS/MS assays. It was concluded that a neutral pH (pH 7.0) is necessary for the analysis of prenylflavanoids, in order to maintain the stability of compounds for at least 24 h. The addition of ascorbic acid to the media improved stability, calibration curves, coefficients of correlation, accuracy, and precision parameters. Mix-mode cation exchange sorbent yielded the best matrix effect factors and recoveries. Method validation results showed appropriate intraday and interday accuracy and precision (<15%). Recovery of isoxanthohumol, xanthohumol, and 8-prenylnaringenin was 97.1% ± 0.03, 105.8% ± 0.05, and 105.4% ± 0.04, respectively, and matrix effect factors were nearly 100%. The stability assay showed that analytes were stable for at least 24 h. The method was applied to quantify 10 human samples of urine and was able to quantify prenylflavanoids in urine after the consumption of a single dose of beer (330 mL).
机译:近年来,由于其作为强力植物雌激素和有效的化学预防剂的生物学活性,对啤酒花和啤酒中的异戊二烯类黄酮,异黄腐酚,黄腐酚和8-异戊烯基柚皮苷的研究兴趣有所增加。但是,异戊二烯类黄酮的行为与大多数多酚不同,因为它们在酸性pH下不稳定。据我们所知,迄今为止,尚未有公开的研究考虑过这些化合物在分析过程中的降解。在目前的工作中,基于固相萃取和液相色谱结合电喷雾电离三重四极杆质谱(LC-ESI-MS / MS)的一种新的灵敏,特异的方法得到了开发和验证。在整个分析过程中,对新方法进行了优化,以避免所选分析物,异黄腐酚,黄腐酚和8-异戊烯基柚皮素的降解,并降低LC-ESI-MS / MS分析中尿液基质的影响。得出的结论是,分析异戊二烯类黄酮需要中性的pH值(pH 7.0),以保持化合物的稳定性至少24 h。向介质中添加抗坏血酸可改善稳定性,校准曲线,相关系数,准确性和精密度参数。混合模式阳离子交换吸附剂产生最佳的基质效应因子和回收率。方法验证结果显示适当的日内和日间准确性和精密度(<15%)。异黄腐酚,黄腐酚和8-异戊烯基柚皮苷的回收率分别为97.1%±0.03、105.8%±0.05和105.4%±0.04,基质效应因子接近100%。稳定性测定表明分析物稳定至少24小时。该方法用于定量10个人的尿液样本,并且能够定量消耗单剂量啤酒(330 mL)后尿液中的异戊二烯类黄酮。

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