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机构地区:[1]广东石油化工学院化学与生命科学学院 [2]茂名出入境检验检疫局,茂名525000 [3]华南师范大学生命科学学院,广东省植物发育生物工程重点实验室,广州510631
出 处:《天然产物研究与开发》2014年第5期699-703,712,共6页Natural Product Research and Development
基 金:广东省科技计划项目(2011B020310008);广东省自然科学基金(S201101000368)
摘 要:采用HPLC-DAD和UPLC-MS/MS对蔓花生中白藜芦醇、白藜芦醇苷和二苯乙烯苷三种二苯乙烯类化合物进行鉴定,建立HPLC-DAD同时测定三种化合物含量的方法。HPLC-DAD分析采用依利特ODS1色谱柱,柱温40℃,流动相A为甲醇,B为1%乙酸水溶液,流速1.0 mL/min。UPLC-MS/MS采用ACQUITY UPLC BEH C18色谱柱,流动相A为乙腈,B为水,电喷雾离子源,负离子检测,数据采集方式为多反应监测模式(MRM)。结果表明:蔓花生根、茎和叶中白藜芦醇含量分别为66.28、90.83和81.56μg/g,白藜芦醇苷含量分别为123.78,302.77和236.53μg/g,根和茎中二苯乙烯苷含量分别为673.60和764.65μg/g,叶中未检测到二苯乙烯苷。Simultaneous determination of 3 stilbene compounds, namely resveratrol, polydatin and stilbene glucoside (2, 3,5,4'-tetra-hydroxT-stilbene-2-O-β-D-gluceside) from Arachis duranensis was performed using HPLC-DAD and UPLC- MS/MS. The experimental conditions for I-IPLC-DAD analysis were as follows: ODS1 column (250mm × 4.6 mm 5 μm) ; column temperature, 40℃ ; mobile phase A, methanol; mobile phase B, 1% aqueous acetic acid; flow rate, 1.0 mL/min; DAD scanning wavelength, 190-400 nm; detection wavelength, 303 nm. The UPLC-MS/MS conditions were as follows :ACQU1TY UPI.,C BEH Cls column (2.1 mmx 50 ram,1.7 pln) ;mobile phase A,acetonitrile;mobile phase B, water;ion source, ESI (negative ion mode). UPLC-MS/MS data were collected using multiple reaction monitoring (MRM) mode. The results showed that resveratrel contents were 66.28,90.83 and 81.56 μg/g,polydatin contents were 123.78,302.77 and 236.53μg/g, in roots, stems and leaves of A. duranens/s, respectively. The content stilhene glucoside in roots and stems was 673.60 and 764.65 μg/g,respectively,but was not detected in leaves.
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