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通过固相萃取-液相色谱/电喷雾电离-八极杆-正交加速飞行时间质谱和新型薄层色谱生物自显影技术对天然来源的乙酰胆碱酯酶抑制剂进行高效、选择性和灵敏的分子筛选。

Highly efficient, selective and sensitive molecular screening of acetylcholinesterase inhibitors of natural origin by solid-phase extraction-liquid chromatography/electrospray ionisation-octopole-orthogonal acceleration time-of-flight-mass spectrometry and novel thin-layer chromatography-based bioautography.

作者信息

Mroczek Tomasz

机构信息

Department of Pharmacognosy with Medicinal Plant Laboratory Unit, Lublin, Poland.

出版信息

J Chromatogr A. 2009 Mar 20;1216(12):2519-28. doi: 10.1016/j.chroma.2009.01.061. Epub 2009 Jan 23.

Abstract

Highly efficient, selective and sensitive molecular screening of natural acetylcholinesterase (AChE) inhibitors was developed and comprised optimized pressurized liquid extraction (PLE) of plant materials followed by highly selective solid-phase extraction (SPE) using Oasis HLB cartridges. Pure alkaloidal fractions were analyzed by a newly developed high-performance liquid-chromatography (HPLC) on a 3 microm Atlantis HILIC silica stationary phase combined with recently introduced electrospray ionisation (ESI) octopole-orthogonal acceleration time-of-flight (oa TOF)-mass spectrometry (MS) with high mass accuracy (about 2 ppm) and high sensitivity (absolute limit of detection (LOD) for galanthamine was about 43 fg at signal-to-noise 13:1). Moreover, a newly developed and validated TLC-bioautography permit galanthamine sensitivities at pg levels. In this way, more potent than galanthamine AChE inhibitor namely 1,2-dihydrogalanthamine in Narcissus jonquilla 'Pipit' extract could be found (with IC(50) value 0.19 microM lower of about 42% than that of galanthamine).

摘要

开发了一种高效、选择性和灵敏的天然乙酰胆碱酯酶(AChE)抑制剂分子筛选方法,该方法包括对植物材料进行优化的加压液体萃取(PLE),然后使用Oasis HLB柱进行高选择性固相萃取(SPE)。通过在3微米Atlantis HILIC硅胶固定相上进行新开发的高效液相色谱(HPLC),结合最近引入的具有高质量准确度(约2 ppm)和高灵敏度(加兰他敏的绝对检测限(LOD)在信噪比为13:1时约为43 fg)的电喷雾电离(ESI)八极杆-正交加速飞行时间(oa TOF)质谱(MS),对纯生物碱馏分进行分析。此外,一种新开发并经过验证的薄层色谱-生物自显影法能够检测到皮克水平的加兰他敏敏感性。通过这种方式,在水仙‘Pipit’提取物中发现了比加兰他敏更有效的AChE抑制剂,即1,2-二氢加兰他敏(其IC(50)值为0.19 microM,比加兰他敏低约42%)。

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