首页> 外文期刊>Analytical and bioanalytical chemistry >Online coupling solid-phase ligand-fishing with high-performance liquid chromatography-diode array detector-tandem mass spectrometry for rapid screening and identification of xanthine oxidase inhibitors in natural products
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Online coupling solid-phase ligand-fishing with high-performance liquid chromatography-diode array detector-tandem mass spectrometry for rapid screening and identification of xanthine oxidase inhibitors in natural products

机译:在线耦合固相配体捕捞与高效液相色谱-二极管阵列检测器-串联质谱联用,用于快速筛选和鉴定天然产物中的黄嘌呤氧化酶抑制剂

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摘要

Screening and analysis of bioactive compounds from natural products is challenging work due to their complexity. This study presents the first report on hyphenation of solid-phase ligand-fishing using immobilized xanthine oxidase microcolumn (IXOM) and high-performance liquid chromatography-diode array detector-tandem mass spectrometry (HPLC-DAD-MS/MS) for screening and identification of XO inhibitors from complex mixtures. Solid-phase ligand-fishing system was hyphenated with the HPLC system via four-port switching valve and a six-port injection valve as an interface for transferring effluents from IXOM to HPLC, and collecting chromatograms from LFMC (ligand-fishing microextraction column) and C-18 column in a run by only one DAD. Mixtures containing allopurinol (positive control) and tryptophane (negative control) were analyzed in order to verify the specificity and reproducibility of the approach. Subsequently, the newly developed system was applied to screening and identification of XO inhibitors from L. macranthoides and its human microsomal metabolites. Six prototype compounds (3-caffeoylquinic acid, 5-caffeoylquinic acid, 4-caffeoylquinic acid, 3,4-dicaffeoylquinic acid, 3,5-dicaffeoylquinic acid, 4,5-dicaffeoylquinic acid) and three metabolites (3-caffeoyl-epi-quinic acid, 5-caffeoyl-epi-quinic acid, 4-caffeoyl-epi-quinic acid) with XO binding affinities were identified. The XO inhibition activities of six prototype compounds were evaluated and confirmed using in vitro enzymatic assay. With the online system developed here, we present a feasible, selective, and effective strategy for rapid screening and identification of enzyme inhibitors from complex mixtures.
机译:从天然产物中筛选和分析生物活性化合物由于其复杂性而具有挑战性。这项研究提供了关于使用固定的黄嘌呤氧化酶微柱(IXOM)和高效液相色谱-二极管阵列检测器-串联质谱(HPLC-DAD-MS / MS)进行固相配体捕捞联用的第一篇报道来自复杂混合物的XO抑制剂。固相配体-捕捞系统通过四端口切换阀和六端口进样阀与HPLC系统联用,作为从IXOM到HPLC转移流出物并收集LFMC(配体捕捞微萃取柱)色谱图的接口C-18色谱柱仅由一个DAD运行。分析了含有别嘌醇(阳性对照)和色氨酸(阴性对照)的混合物,以验证该方法的特异性和可重复性。随后,新开发的系统被用于筛选和鉴定来自L. macranthoides及其人类微粒体代谢物的XO抑制剂。六个原型化合物(3-咖啡酰基奎宁酸,5-咖啡酰基奎宁酸,4-咖啡酰基奎宁酸,3,4-二咖啡酰基奎宁酸,3,5-二咖啡酰基奎宁酸,4,5-二咖啡酰基奎宁酸)和三种代谢物(3-咖啡酰基-表-鉴定了具有XO结合亲和力的苯甲酸,5-咖啡酰基-表奎宁酸,4-咖啡酰基-表奎宁酸,4-咖啡酰基-表奎宁酸。使用体外酶法评估并确认了六个原型化合物的XO抑制活性。通过此处开发的在线系统,我们提出了一种可行,选择性和有效的策略,用于从复杂混合物中快速筛选和鉴定酶抑制剂。

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