首页> 外文期刊>Journal of chromatography, A: Including electrophoresis and other separation methods >An improved method for a fast screening of alpha-glucosidase inhibitors in cherimoya fruit (Annona cherimola Mill.) applying effect-directed analysis via high-performance thin-layer chromatography-bioassay-mass spectrometry
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An improved method for a fast screening of alpha-glucosidase inhibitors in cherimoya fruit (Annona cherimola Mill.) applying effect-directed analysis via high-performance thin-layer chromatography-bioassay-mass spectrometry

机译:快速筛选亚硫咖啡果(Annona Cherimola Mill)的快速筛选α-葡萄糖苷酶抑制剂的改进方法。通过高性能薄层色谱 - 生物测定 - 质谱法应用效果效应分析

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alpha-glucosidase inhibitors (AGIs) are very attractive bioactive compounds due to their therapeutic profile that includes beneficial effects over glycemic control in type 2 diabetes mellitus and viral infections. Its detection and identification in plants and fruits has gained growing attention, and certainly requires efficient screening methodologies. The objective of the present work was to develop a fast methodology to detect and identify AGIs in cherimoya fruit (Annona cherimola Mill.) applying effect-directed analysis via high-performance thin layer-chromatography (HPTLC) linked with bioassay and mass spectrometry (MS). Both, HPTLC and bioassay conditions, were optimized accomplishing 50% and 83% reduction on enzyme concentration and incubation time respectively, compared to the original method. Additionally, the contrast between inhibitory bands and purple background was also enhanced by enzyme substrate impregnation on HPTLC plate. The optimized detection conditions established were the following: 5.0 U mL(-1) of enzyme solution, 1.0 mg mL(-1) of 2-naphthyl-alpha-D-glucopyranoside substrate, 1.0 mg mL(-1) of Fast Blue B salt solution and 10 min as incubation time. Applying this methodology, coupled to HPTLC-MS and ultra-high-performance liquid chromatography (UHPLC)-diode array detector (DAD)-MS/MS, it was possible for the first time to detect and identify three AGIs in cherimoya peel and seeds. Compounds were tentatively assigned as phenolamides (phenylethyl cinnamides): N-trans-feruloyl tyramine (m/z 314 [M+H](+) ; UV lambda(max) 293 and 316 nm), N-trans-p-coumaroyl tyramine (m/z 284 [M+H](+) ; UV lambda(max) 296nm) and N-trans-feruloyl phenethylamine (m/z 298 [M+H](+) ; UV lambda(max) 288 nm). To the best of our knowledge, the presence of latter compound is reported for the first time in cherimoya. (C) 2019 Elsevier B.V. All rights reserved.
机译:α-葡萄糖苷酶抑制剂(AGIS)是非常有吸引力的生物活性化合物由于其包括在血糖控制在2型糖尿病和病毒感染的有益作用它们的治疗分布。它的检测和鉴定的植物和水果已经获得了越来越多的关注,当然也需要有效的筛选方法。本工作的目的是开发一种快速的方法来检测和番荔枝果实识别AGIS(番荔枝cherimola轧机。)将效果定向经由高性能薄层色谱法(HPTLC)与生物测定法和质谱联分析(MS )。既,HPTLC和生物测定的条件下,进行了优化完成50%,并且在分别酶浓度和温育时间%的减少83,相比于原来的方法。此外,抑制性带和紫色的背景之间的对比度是通过对HPTLC板的酶底物浸渍增强。建立优化的检测条件如下:酶溶液5.0毫升ü(-1),1.0毫克的2-萘基的α-d-D-吡喃葡糖苷底物溶液(-1),1.0毫克毫升(-1)固蓝B的盐溶液和10分钟作为温育时间。采用这个方法,其耦合到HPTLC-MS和超高效液相色谱法(UHPLC)-diode阵列检测器(DAD)-MS / MS,有可能在第一次检测和番荔枝果皮和种子确定3个AGIS 。化合物暂定为phenolamides(苯乙基肉桂酰胺):N-反式 - 阿魏酰酪胺(M / Z 314 [M + H](+); UV拉姆达(最大值)293和316纳米),N-反式 - 对香豆酰基酪胺(M / Z 284 [M + H](+); UV拉姆达(最大值)296nm)和N-反式 - 阿魏酰苯乙胺(M / Z 298 [M + H](+); UV拉姆达(最大值)288 nm)的。据我们所知,后者化合物的存在报道中番荔枝首次。 (c)2019 Elsevier B.v.保留所有权利。

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