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A new method for screening aldose reductase inhibitors using ultrahigh performance liquid chromatography-tandem mass spectrometry

机译:超高效液相色谱-串联质谱法筛选醛糖还原酶抑制剂的新方法

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In this study, an ultrahigh performance liquid chromatography and tandem mass spectrometry (UPLC-MS/ MS) method was developed for the detection of aldose reductase (AR) activity and the screening of AR inhibitors in vitro. Glucose was chosen as the substrate of the enzymatic reaction system according to the polyol pathway. In the polyol pathway, glucose could be converted into sorbitol. The multiple reaction monitoring (MRM) mode was used to directly detect the level of sorbitol from each analyte and the amount of sorbitol could be reduced via the addition of an inhibitor. The proposed approach had been successfully applied to determine the AR inhibitory activities of epalrestat, flavonoids and natural product extracts. Additionally, we proposed a detailed discussion of the structure-activity relationships of flavonoids according to the inhibitory activities of thirty-two flavonoids. The screening method proposed in our study was similar to the metabolic pathway in diabetic patients and could eliminate the interference of other substances. We could envision that our method could be used for the screening of AR inhibitors as drugs for the treatment of related diabetic complications.
机译:在这项研究中,开发了一种超高效液相色谱和串联质谱(UPLC-MS / MS)方法,用于检测醛糖还原酶(AR)活性并在体外筛选AR抑制剂。根据多元醇途径,选择葡萄糖作为酶促反应系统的底物。在多元醇途径中,葡萄糖可以转化为山梨糖醇。多反应监测(MRM)模式用于直接检测每种分析物的山梨醇水平,可通过添加抑制剂来减少山梨醇的量。所提出的方法已成功应用于确定依帕司他,类黄酮和天然产物提取物的AR抑制活性。此外,我们根据32种黄酮类化合物的抑制活性,对黄酮类化合物的构效关系进行了详细讨论。我们研究中提出的筛选方法与糖尿病患者的代谢途径相似,可以消除其他物质的干扰。我们可以设想,我们的方法可用于筛选AR抑制剂,作为治疗相关糖尿病并发症的药物。

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