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Screening of xanthine oxidase inhibitors in complex mixtures using online HPLC coupled with postcolumn fluorescencebased biochemical detection

机译:使用在线HPLC结合柱后荧光生化检测筛选复杂混合物中的黄嘌呤氧化酶抑制剂

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摘要

Xanthine oxidase (XO) catalyzes the metabolism of hypoxanthine and xanthine to uric acid, the overproduction and/or underexcretion of which could cause the incidence of hyperuricemia such as gout. Herein, the inhibition of XO is recognized as one of the therapeutic approaches to treat gout. In the present study, an off-line fluorescence-based microplate method was first developed for an XO assay in which the enzyme converted pterin to its fluorescent metabolite isoxanthopterin. Then, a postcolumn continuous XO assay as a means of bioactivity assessment was coupled to HPLC separation to establish the online HPLC with diode array detection, biochemical detection, and MS/MS system for the screening of XO inhibitors. The availability of the online system was first tested with a positive drug, allopurinol, a well-known XO inhibitor, and subsequent analysis of Scutellaria baicalensis extract showed that two main bioactive compounds with XO inhibitory activities were observed, indicating that the developed online system was applicable to complex mixtures.
机译:黄嘌呤氧化酶(XO)催化次黄嘌呤和黄嘌呤代谢为尿酸,其过度产生和/或排泄不足会导致高尿酸血症(如痛风)的发生。在此,XO的抑制被认为是治疗痛风的治疗方法之一。在本研究中,首先开发了基于离线荧光的微孔板方法用于XO分析,其中酶将蝶呤转化为荧光代谢产物异黄蝶呤。然后,将作为生物活性评估手段的柱后连续XO测定与HPLC分离相结合,以建立具有二极管阵列检测,生化检测和用于XO抑制剂筛选的MS / MS系统的在线HPLC。首先使用阳性药物别嘌醇(一种著名的XO抑制剂)测试了在线系统的可用性,随后对黄cut提取物进行的分析表明,观察到了两种具有XO抑制活性的主要生物活性化合物,表明开发的在线系统适用于复杂混合物。

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