The extraction and determination of cytisine, sophocarpine, matrine, sophoridine and oxymatrine in Sophora flavescens Ait. were performed using subcritical water extraction and capillary electrophoresis with field-amplified sample stacking. The effects of extraction temperature, pressure, time and cycle number on the extraction yields were investigated systematically for accelerated solvent extraction with ethanol (ASE) and accelerated solvent extraction with water (subcritical water extraction, SWE). The extraction yields obtained using SWE, ASE, water ultrasonic extraction and chloroform soaking extraction methods were compared. The electrophoresis separation buffer was monosodium phosphate (pH 3.0; 110 mM)-isopropanol (85:15, v/v). The effect of phosphoric acid added to the sample matrix on the reproducibility of the peak heights of the analytes was also examined. Cytisine, sophoridine and oxymatrine showed good linearity (R(2)>0.999) within 0.125-4.0 μg/mL, and sophocarpine and matrine exhibited good linearity (R(2)>0.998) within 0.0625-2.0 μg/mL, with the detection limits in the range of 0.004-0.0013 μg/mL. The five alkaloid contents in medicinal plants from different sources and Sophora instant granule were determined and compared.

译文

苦参中的胞苷,槐果碱,苦参碱,槐定碱和氧化苦参碱的提取和测定。使用亚临界水萃取和毛细管电泳进行现场扩增样品堆积。系统研究了乙醇加速溶剂萃取 (ASE) 和水加速溶剂萃取 (亚临界水萃取,SWE) 提取温度,压力,时间和循环次数对提取收率的影响。比较了SWE,ASE,水超声提取和氯仿浸泡提取方法获得的提取率。电泳分离缓冲液是磷酸一钠 (pH 3.0; 110 mM)-异丙醇 (85:15,v/v)。还检查了添加到样品基质中的磷酸对分析物峰高重现性的影响。Cytisine,槐定碱和氧化苦参碱在0.125-4.0 μ g/mL范围内显示出良好的线性 (R(2)>0.999),而槐果碱和苦参碱在0.0625-2.0 μ g/mL范围内显示出良好的线性 (R(2)>0.998),检出限在0.004-0.0013 μ g/mL范围内。测定并比较了不同来源药用植物和苦参速溶颗粒中五种生物碱的含量。

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